Spinal Muscular AtrophyRESISTANTNCT05632666
Respiratory Muscle Training in Patients With Spinal Muscular Atrophy (SMA).
A study testing Inspiratory and expiratory muscle training at a therapeutic intensity and Inspiratory and expiratory muscle training at a non-therapeutic intensity in people with Spinal Muscular Atrophy, run by UMC Utrecht at 1 site in Netherlands.
Trial summary
The goal of this clinical trial is to study respiratory muscle training in patients with Spinal Muscular Atrophy (SMA). The main questions it aims to answer are: Is a home-based individualized training program for the inspiratory and expiratory muscles feasible (good adherence and good acceptability)? Can a home-based… Read more about this study
- Who is it for?
- Ages 8 years and older
- Conditions the study is for
- Spinal Muscular Atrophy
- What is being tested?
- Inspiratory and expiratory muscle training at a therapeutic intensity and Inspiratory and expiratory muscle training at a non-therapeutic intensity
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 30 participants
- Where
- 1 siteNetherlands
- Study dates
- 2 Feb 2021to 31 Jan 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 8 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Age ≥ 8 years;
- Respiratory muscle weakness (PImax ≤80 cmH2O (31));
- Maintenance dose (≥2 months) Spinraza® or (≥2 months) Risdiplam or no treatment;
- Given oral and written informed consent when ≥18 years old and additional informed consent by the parents or legal representative if the participant is <16 years old.
Who cannot join
- Inability to perform respiratory and/or lung-function testing;
- Inability to understand Dutch or English;
- A history of pneumothorax or symptomatic low cardiac output syndrome;
- Treatment period < 2 months of Spinraza® or Risdiplam
Trial locations and contacts
1 site in 1 country.
About this study
The goal of this clinical trial is to study respiratory muscle training in patients with Spinal Muscular Atrophy (SMA). The main questions it aims to answer are:
- Is a home-based individualized training program for the inspiratory and expiratory muscles feasible (good adherence and good acceptability)?
- Can a home-based individualized training program for the inspiratory and expiratory muscles increase the strength of these muscles? Participants will be asked to perform 10 training sessions per week, spread out over 5-7 days. Each training session consists of 30 breathing cycles through the inspiratory muscle trainer and 30 breathing cycles trough the expiratory muscle trainer.
Read more
In the first four months of the study researchers will compare two groups to see if a higher trainings load is more effective.
One group will start at a trainings load of 10% of their maximal inspiratory and expiratory muscle strength.
The other group will start at a trainings load of 30% of their maximal inspiratory and expiratory muscle strength. This group also need to adjust the trainings load based on their perceived exertion.
After four months all participants will train on a trainings load of 30% of their maximal inspiratory and expiratory muscle strength and adjust the trainings load based on their perceived exertion.
The participants will come to the hospital for lung function tests every four months for 12 months.
Read the detailed description
The aim of this study is to assess the feasibility and efficacy of respiratory muscle training in patients with SMA and respiratory muscle weakness. The hypothesis is that an individualized incremental home-based respiratory muscle training program will be feasible and will improve inspiratory muscle strength, expiratory muscle strength, lung function and patient reported breathing difficulties in patients with SMA.
Study setting: This study is conducted at the outpatient department of the Netherlands SMA center and the Child Development and Exercise Center at the University Medical Center Utrecht (UMCU), The Netherlands. All members of the study team, consisting of physicians, physiotherapists, lung function technicians, clinical exercise physiologists and nurses, have broad experience with SMA due to the national cohort study that is carried out in this center since 2010.
Study design: The RESISTANT study is an investigator-initiated, mono-center study consisting of two parts:
Part 1 (0-4 months): a single blinded randomized sham-controlled trial (RCT). In the first part of the study, the feasibility and efficacy of respiratory muscle training (RMT) in patients with SMA will be determined.
Before the first visit, participants will be recruited for enrollment by a research nurse. Patients who express interest in participating receive a patient information letter and an appointment with the physiotherapist. At the first visit (M0), the physiotherapist further determines whether patients are eligible for participation. After signing the informed consent form, participants are weighed and their length is determined, followed by lung function tests. If the maximum inspiratory mouth pressure (PImax) >80 centimeter of Water Column (cmH2O), participants are excluded for the study. If PImax ≤ 80 cmH2O, participants will be stratified prior to randomization based on PImax (group 1: PImax <60 cmH2O, group 2: PImax ≥60 cmH2O, 60 cmH2O was the median PImax in the group of patients used for the natural history study). Participants will be randomly allocated to the intervention or sham-control group. A variable block randomization method with allocation concealment in a centralized system will be used for randomization. The lung function analyst is blinded for treatment allocation. A data analyst will design and sign the data analysis plan in advance. The data will be analyzed according to the analysis plan by a physiotherapist who is not blinded for treatment allocation. The physiotherapists who will perform the two-weekly telephone calls are not blinded for treatment allocation. Patients will know that there are two treatment groups, and they are informed that it is not yet known which treatment is most effective.
All participants (and parents) will be instructed by a trained physiotherapist on the use of both devices at the first visit (baseline or M0). Participants are instructed to aim for 10 training sessions per week, divided over 5 to 7 days. A minimum of 6 hours in between training sessions is recommended. Per training session, the participant breathes 30 times through the POWERbreathe (inspiratory muscle training) and 30 times through the reverse Threshold® IMT (expiratory muscle training). If necessary, the participant may take a break, with a maximum of 60 seconds after 10 or 15 breaths. After each session they fill in a diary, which contains information about the load and the perceived exertion (Borg scale 0-10).
In the active treatment group, the intensity of the training is set at M0 at 30% of PImax and maximum expiratory mouth pressure (PEmax) and will be increased or decreased based on level of perceived exertion. Participants are instructed to increase the intensity with 1-5 cmH2O if they score a perceived exertion of 0-4 and decrease the intensity if they score a perceived exertion of 7-10. If they score a perceived exertion of 5 or 6, the intensity will not me adjusted. The intensity of the training in the sham-controlled group will be set at M0 at 10% of PImax and PEmax and will remain the same during the first 4 months of training.
- Inspiratory muscle trainer: For the inspiratory muscle training (IMT) the Conformité Européenne certified POWERbreathe KHP2 is used. Clinical research has shown high participant motivation and adherence to training with the POWERbreathe KHP2 thanks to the on-screen feedback. Furthermore, healthcare professionals can review participant progress by tracking up to 30 of the participants training sessions which the KHP2 is able to store. This data can be scrolled through to monitor progress. The electronic, variable, tapered flow valve ensures maximum training benefit. It is easy to use, easy to clean and training improvements can be easily monitored.
- Expiratory muscle trainer: For the expiratory muscle training (EMT) the Threshold Inspiratory Muscle Trainer (IMT) (Philips Respironics) in reverse is used. Use of the Threshold Positive Expiratory Pressure (PEP) (Philips Respironics) is one method to perform EMT. However, the maximal expiratory resistance of the Threshold PEP is limited to 20 cmH20. To overcome this limitation in expiratory resistance, the Threshold IMT will be used in reverse. This device contains, at its end, a valve closed by the positive pressure of a spring, which can be graded from 9 to 41 cmH2O and allows resistance changes by 1 cmH2O increments. The reverse Threshold IMT has a one-way spring-loaded valve, that closes during expiration and requires that participants exhale hard enough, to open the valve and let the air go out. This device provides constant pressure for expiratory muscle training, regardless of how quickly or slowly the participant breathes, and the optimal loading pressure can be adjusted, based upon the individual characteristics of the participant.
Part 2 (5-12 months): open label extension phase. In the second part of the study, the sham-control group will be provided with a supervised RMT at a therapeutic intensity of 30% of PImax and PEmax and the long-term effects of RMT on the occurrence of respiratory infections, health related quality of life and feasibility will be investigated in the active treatment and sham-controlled group.
Participants will visit our outpatient department every 4 months for 12 months after inclusion for assessment of primary and secondary outcome measures. This study is currently ongoing; the first participant was included on 2-2-2021. Study completion is expected in the first quarter of 2023.
Sample size: Based on a previous report on inspiratory muscle training in patients with neuromuscular diseases (n=27, 18 patients with Duchenne Muscular Dystrophy (DMD) and 9 patients with SMA) indicating a mean improvement in PImax of 28 cmH2O difference (SD ±26.27), a mean difference of 20 cmH2O (SD 25.0) is assumed between active and sham treated patients after 4 months. To detect this effect size with 80% power and two-sided alpha of 5%, 50 patients are needed (25 per group).
Statistical analysis: Continuous variables will be expressed as means with standard deviations or medians with interquartile ranges (whichever is more appropriate), and discrete variables will be expressed as numbers with percentages. The main efficacy population will consist of all patients being randomized and analyzed according to their original treatment allocation, irrespective of actual received treatment or follow-up (intention-to-treat). The primary comparison will be the mean difference in PImax at month 4. An ANCOVA model will be used to analyze the differences between groups adjusting for baseline PImax. Missing data in the outcomes at month 4 will be imputed by the baseline-observation-carried-forward (BOCF) approach. This will be a conservative method because expected is that patients' PImax will improve after training. For the longitudinal data, a mixed model will be used for repeated measurements including a term for visit, treatment, their interaction, and baseline PImax to account for the correlation within subjects. Similar models will be used for the secondary endpoints. The incidence of adverse events will be summarized by treatment group and in all treatment groups combined in frequency tables, coded according to the introductory guide Medical Dictionary for Regulatory Activities (MedDRA) version 21.0.
Data management: The following measures will be taken to assure the confidentiality and anonymity of the participants' data or documents collected in Castor: a) each participant will be identified in an electronic database by a unique six digit code; b) the list of participant names corresponding to the codes will be stored in a separate encrypted electronic database, safeguarded by the principal investigator; c) only study investigators will have access to the databases and examine individual data or documents; d) all logins will be recorded; e) adopt strict precautions to prevent access to the data or documents by non-authorized persons; f) the handling of data and documents will comply with the General data protection regulation (GDPR) and is further described in the Data Monitoring Plan.
Ethics, dissemination, and safety monitoring: The investigator obtains written informed consent before study participation from participants and from parents if the participant is <16 years old.
The trial is monitored by an external independent party (Julius Clinical). Because of the negligible risk classification minimal monitoring will be necessary. All participants are insured by the sponsor in case of harm due to study participation.
The study will be conducted according to the principles of the Declaration of Helsinki, adapted 19-10-2013, and in accordance with the Medical Research Involving Human Subjects Act (WMO). The code of Conduct as agreed upon 2001 by the Dutch organization of Pediatrics will be used. The study is partly done by minors, which means that in any case of resistance the test and research protocol will be terminated. Resistance means that the patient's behavior obviously differs from or is more excessive compared to participant's normal behavior. The national rules of the Dutch Association of Pediatrics for protection of minor study participants, are followed during the entire study. The results of this study will be publicly disclosed in several publications in peer reviewed scientific journals related to the topic of this study and orally in conferences concerning this theme.
- Conditions
- Spinal Muscular Atrophy
- Being tested
- Inspiratory and expiratory muscle training at a therapeutic intensity, Inspiratory and expiratory muscle training at a non-therapeutic intensity
- Keywords
- Spinal Muscular Atrophy, Inspiratory Muscle Training, Expiratory Muscle Training, Maximum Inspiratory Mouth Pressure, Maximum Expiratory Mouth Pressure, Respiratory Muscle Training
- Medical subject headings
- Muscular Atrophy, Spinal
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Inspiratory and expiratory muscle training at a therapeutic intensityOther
The active treatment group will receive inspiratory muscle training starting at a therapeutic intensity of 30% of maximum inspiratory mouth pressure (PImax) and expiratory muscle training starting at a therapeutic intensity of 30% of maximum expiratory mouth pressure (PEmax) for 4 months.
In the active treatment group, the inspiratory and expiratory threshold (intensity) will be adjusted to the perceived exertion (measured with a Borg scale).
Inspiratory and expiratory muscle training at a non-therapeutic intensityOther
The sham-control group will receive the same training protocol as the active treatment group but with a low (10% of PImax and PEmax) and stable non-therapeutic intensity.
| Study group | Role | What they receive |
|---|---|---|
| Active treatment group | Experimental | Not described Receives: Other: Inspiratory and expiratory muscle training at a therapeutic intensity |
| Sham-controlled group | Sham comparator | Not described Receives: Other: Inspiratory and expiratory muscle training at a non-therapeutic intensity |
What is being measured
The primary outcome is the main question the study is designed to answer.
Maximal inspiratory mouth pressure (PImax)
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: Baseline
Maximal inspiratory mouth pressure (PImax)
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: 4 months
Maximal inspiratory mouth pressure (PImax)
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: 8 months
Maximal inspiratory mouth pressure (PImax)
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: 12 months
Feasibility: adherence from baseline (M0) to 4 months visit (M4)
The completion rate of the estimated number of training sessions over 4 months (>80% of the participants have fulfilled the prescribed treatment = good adherence). Adherence will be monitored by a patient diary, the data saved in the POWERbreathe KHP2 and, two weekly telephone- or video calls by a physiotherapist.
Measured: From baseline (M0) to 4 months visit (M4)
Feasibility: adherence from 4 months (M4) to 8 months visit (M8)
The completion rate of the estimated number of training sessions over 4 months (>80% of the participants have fulfilled the prescribed treatment = good adherence). Adherence will be monitored by a patient diary, the data saved in the POWERbreathe KHP2 and, two weekly telephone- or video calls by a physiotherapist.
Measured: From 4 months (M4) to 8 months visit (M8)
Feasibility: adherence from 8 months (M8) to 12 months visit (M12)
The completion rate of the estimated number of training sessions over 4 months (>80% of the participants have fulfilled the prescribed treatment = good adherence). Adherence will be monitored by a patient diary, the data saved in the POWERbreathe KHP2 and, two weekly telephone- or video calls by a physiotherapist.
Measured: From 8 months (M8) to 12 months visit (M12)
Feasibility: acceptability
The willingness to continue the training (>5 = good acceptability) assessed with a Borg Scale (0-10)
Measured: 4 months
Feasibility: acceptability
The willingness to continue the training (>5 = good acceptability) assessed with a Borg Scale (0-10)
Measured: 8 months
Feasibility: acceptability
The willingness to continue the training (>5 = good acceptability) assessed with a Borg Scale (0-10)
Measured: 12 months
Secondary outcomes (54)
Maximal expiratory mouth pressure (PEmax)
Maximal expiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: Baseline
Maximal expiratory mouth pressure (PEmax)
Maximal expiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: 4 months
Maximal expiratory mouth pressure (PEmax)
Maximal expiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: 8 months
Maximal expiratory mouth pressure (PEmax)
Maximal expiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Measured: 12 months
Health related quality of life
Health related quality of life will be measured with the 36-item Short Form Health Survey (SF36) for adults and the Pediatric Quality of Life Inventory (PedsQL) for children and their parents/caregivers.
Measured: Baseline
Health related quality of life
Health related quality of life will be measured with the 36-item Short Form Health Survey (SF36) for adults and the Pediatric Quality of Life Inventory (PedsQL) for children and their parents/caregivers.
Measured: 4 months
Health related quality of life
Health related quality of life will be measured with the 36-item Short Form Health Survey (SF36) for adults and the Pediatric Quality of Life Inventory (PedsQL) for children and their parents/caregivers.
Measured: 8 months
Health related quality of life
Health related quality of life will be measured with the 36-item Short Form Health Survey (SF36) for adults and the Pediatric Quality of Life Inventory (PedsQL) for children and their parents/caregivers.
Measured: 12 months
Forced vital capacity (FVC)
Forced vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: Baseline
Forced vital capacity (FVC)
Forced vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 4 months
Forced vital capacity (FVC)
Forced vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 8 months
Forced vital capacity (FVC)
Forced vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 12 months
Slow vital capacity (SVC)
Slow vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: Baseline
Slow vital capacity (SVC)
Slow vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 4 months
Slow vital capacity (SVC)
Slow vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 8 months
Slow vital capacity (SVC)
Slow vital capacity in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 12 months
Peak expiratory flow (PEF)
Peak expiratory flow in liters per second assessed conform the ERS/ATS recommendations. Reference values of Quanjer et al. 1993 will be used to calculate % of predicted for adults and Koopman et al. 2011 will be used to calculate % of predicted for kids.
Measured: Baseline
Peak expiratory flow (PEF)
Peak expiratory flow in liters per second assessed conform the ERS/ATS recommendations. Reference values of Quanjer et al. 1993 will be used to calculate % of predicted for adults and Koopman et al. 2011 will be used to calculate % of predicted for kids.
Measured: 4 months
Peak expiratory flow (PEF)
Peak expiratory flow in liters per second assessed conform the ERS/ATS recommendations. Reference values of Quanjer et al. 1993 will be used to calculate % of predicted for adults and Koopman et al. 2011 will be used to calculate % of predicted for kids.
Measured: 8 months
Peak expiratory flow (PEF)
Peak expiratory flow in liters per second assessed conform the ERS/ATS recommendations. Reference values of Quanjer et al. 1993 will be used to calculate % of predicted for adults and Koopman et al. 2011 will be used to calculate % of predicted for kids.
Measured: 12 months
Forced expiratory volume in 1 second (FEV1)
Forced expiratory volume in 1 second in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: Baseline
Forced expiratory volume in 1 second (FEV1)
Forced expiratory volume in 1 second in liters assessed conform the ERS/ATS recommendations.Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 4 months
Forced expiratory volume in 1 second (FEV1)
Forced expiratory volume in 1 second in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 8 months
Forced expiratory volume in 1 second (FEV1)
Forced expiratory volume in 1 second in liters assessed conform the ERS/ATS recommendations. Reference values from Quanjer et al. 2012 will be used to calculate % of predicted.
Measured: 12 months
Peak cough flow (PCF)
Peak cough flow in liters per second assessed conform the ERS/ATS recommendations.
Measured: Baseline
Peak cough flow (PCF)
Peak cough flow in liters per second assessed conform the ERS/ATS recommendations.
Measured: 4 months
Peak cough flow (PCF)
Peak cough flow in liters per second assessed conform the ERS/ATS recommendations.
Measured: 8 months
Peak cough flow (PCF)
Peak cough flow in liters per second assessed conform the ERS/ATS recommendations.
Measured: 12 months
Sniff Nasal Inspiratory Pressure (SNIP)
Sniff Nasal Inspiratory Pressure in Kilopascal (kPa) assessed conform the ERS/ATS recommendations.
Measured: Baseline
Sniff Nasal Inspiratory Pressure (SNIP)
Sniff Nasal Inspiratory Pressure in Kilopascal (kPa) assessed conform the ERS/ATS recommendations.
Measured: 4 months
Sniff Nasal Inspiratory Pressure (SNIP)
Sniff Nasal Inspiratory Pressure in Kilopascal (kPa) assessed conform the ERS/ATS recommendations.
Measured: 8 months
Sniff Nasal Inspiratory Pressure (SNIP)
Sniff Nasal Inspiratory Pressure in Kilopascal (kPa) assessed conform the ERS/ATS recommendations.
Measured: 12 months
Mouth occlusion pressure at 100ms (P0.1)
Mouth occlusion pressure at 100ms during quiet breathing in Kilopascal (kPa). P0.1 is a marker of neuromuscular ventilator drive, which is independent of the patient's effort. Assessed conform the ERS/ATS recommendations. Reference values of Criee 2003 will be used to calculate % of predicted.
Measured: Baseline
Mouth occlusion pressure at 100ms (P0.1)
Mouth occlusion pressure at 100ms during quiet breathing in Kilopascal (kPa). P0.1 is a marker of neuromuscular ventilator drive, which is independent of the patient's effort. Assessed conform the ERS/ATS recommendations. Reference values of Criee 2003 will be used to calculate % of predicted.
Measured: 4 months
Mouth occlusion pressure at 100ms (P0.1)
Mouth occlusion pressure at 100ms during quiet breathing in Kilopascal (kPa). P0.1 is a marker of neuromuscular ventilator drive, which is independent of the patient's effort. Assessed conform the ERS/ATS recommendations. Reference values of Criee 2003 will be used to calculate % of predicted.
Measured: 8 months
Mouth occlusion pressure at 100ms (P0.1)
Mouth occlusion pressure at 100ms during quiet breathing in Kilopascal (kPa). P0.1 is a marker of neuromuscular ventilator drive, which is independent of the patient's effort. Assessed conform the ERS/ATS recommendations. Reference values of Criee 2003 will be used to calculate % of predicted.
Measured: 12 months
P0.1/PImax
The ratio of P0.1/PImax have been suggested as important predictor of impending respiratory muscle fatigue (work of breathing)
Measured: Baseline
P0.1/PImax
The ratio of P0.1/PImax have been suggested as important predictor of impending respiratory muscle fatigue (work of breathing)
Measured: 4 months
P0.1/PImax
The ratio of P0.1/PImax have been suggested as important predictor of impending respiratory muscle fatigue (work of breathing)
Measured: 8 months
P0.1/PImax
The ratio of P0.1/PImax have been suggested as important predictor of impending respiratory muscle fatigue (work of breathing)
Measured: 12 months
Medical Research Council (MRC) dyspnea scale
This scale measures perceived respiratory disability.
Measured: Baseline
Medical Research Council (MRC) dyspnea scale
This scale measures perceived respiratory disability.
Measured: 4 months
Medical Research Council (MRC) dyspnea scale
This scale measures perceived respiratory disability.
Measured: 8 months
Medical Research Council (MRC) dyspnea scale
This scale measures perceived respiratory disability.
Measured: 12 months
Respiratory infections
Respiratory infection frequency (based on the need for antibiotics and/or hospitalization).
Measured: Assessed during the two weekly telephone consultations.
Respiratory infections
Respiratory infection frequency (based on the need for antibiotics and/or hospitalization).
Measured: Assessed during the 4 months visit.
Respiratory infections
Respiratory infection frequency (based on the need for antibiotics and/or hospitalization).
Measured: Assessed during the 8 months visit.
Respiratory infections
Respiratory infection frequency (based on the need for antibiotics and/or hospitalization).
Measured: Assessed during the 12 months visit.
Adverse Events
Adverse Events
Adverse Events
Adverse Events Adverse Events coded according to the introductory guide MedDRA version 21.0
Measured: During the whole 12 months.
Dyspnea immediately after lung function measure and after each training session
Assesses with a Borg scale ranging from 0-10.
Measured: After each training session
Dyspnea immediately after lung function measure and after each training session
Assesses with a Borg scale ranging from 0-10.
Measured: Baseline
Dyspnea immediately after lung function measure and after each training session
Assesses with a Borg scale ranging from 0-10.
Measured: 4 months
Dyspnea immediately after lung function measure and after each training session
Assesses with a Borg scale ranging from 0-10.
Measured: 8 months
Dyspnea immediately after lung function measure and after each training session
Assesses with a Borg scale ranging from 0-10.
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Nov 2022
- Study start2 Feb 2021
- Primary completion31 Jan 2023 (estimated)
- Study completion31 Jan 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (24)Papers the sponsor has linked to this study.
- Other trials for Spinal Muscular AtrophyStudies of the same condition, open and under way.
- More trials run by UMC UtrechtThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- In the first four months of the study, the active treatment group will receive inspiratory muscle training starting at a therapeutic intensity of 30% of maximum inspiratory mouth pressure (PImax) and expiratory muscle training starting at a therapeutic intensity of 30% of maximum expiratory mouth pressure (PEmax). The sham-control group will receive the same training protocol but with a low (10% of PImax and PEmax) non-therapeutic intensity. After four months, the sham-control group will also be provided with a supervised RMT at a therapeutic intensity of 30% of PImax and PEmax.
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- UMC Utrecht
- Sponsor type
- University, hospital or other
- Collaborators
- Princess Beatrix Muscle Foundation
- Responsible party
- Principal investigator, Dr. H.J. (Erik) Hulzebos, UMC Utrecht
- Investigators
- Erik Hulzebos, Dr, Principal investigator, UMC Utrecht
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05632666
- Sponsor's protocol ID
- W.OB19-01
- Acronym
- RESISTANT
- Status last verified
- Nov 2022
- First submitted
- 2 Nov 2022
- Last updated
- 30 Nov 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Wadman RI, Vrancken AF, van den Berg LH, van der Pol WL. Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3. Neurology. 2012 Nov 13;79(20):2050-5. doi: 10.1212/WNL.0b013e3182749eca. Epub 2012 Oct 31.
PubMed 23115209Finkel RS, Sejersen T, Mercuri E; ENMC SMA Workshop Study Group. 218th ENMC International Workshop:: Revisiting the consensus on standards of care in SMA Naarden, The Netherlands, 19-21 February 2016. Neuromuscul Disord. 2017 Jun;27(6):596-605. doi: 10.1016/j.nmd.2017.02.014. Epub 2017 Mar 2. No abstract available.
PubMed 28392274Lunn MR, Wang CH. Spinal muscular atrophy. Lancet. 2008 Jun 21;371(9630):2120-33. doi: 10.1016/S0140-6736(08)60921-6.
PubMed 18572081Verhaart IEC, Robertson A, Wilson IJ, Aartsma-Rus A, Cameron S, Jones CC, Cook SF, Lochmuller H. Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature review. Orphanet J Rare Dis. 2017 Jul 4;12(1):124. doi: 10.1186/s13023-017-0671-8.
PubMed 28676062Wang CH, Finkel RS, Bertini ES, Schroth M, Simonds A, Wong B, Aloysius A, Morrison L, Main M, Crawford TO, Trela A; Participants of the International Conference on SMA Standard of Care. Consensus statement for standard of care in spinal muscular atrophy. J Child Neurol. 2007 Aug;22(8):1027-49. doi: 10.1177/0883073807305788.
PubMed 17761659Stam M, Wadman RI, Wijngaarde CA, Bartels B, Asselman FL, Otto LAM, Goedee HS, Habets LE, de Groot JF, Schoenmakers MAGC, Cuppen I, van den Berg LH, van der Pol WL. Protocol for a phase II, monocentre, double-blind, placebo-controlled, cross-over trial to assess efficacy of pyridostigmine in patients with spinal muscular atrophy types 2-4 (SPACE trial). BMJ Open. 2018 Jul 30;8(7):e019932. doi: 10.1136/bmjopen-2017-019932.
PubMed 30061431Mongiovi P, Dilek N, Garland C, Hunter M, Kissel JT, Luebbe E, McDermott MP, Johnson N, Heatwole C. Patient Reported Impact of Symptoms in Spinal Muscular Atrophy (PRISM-SMA). Neurology. 2018 Sep 25;91(13):e1206-e1214. doi: 10.1212/WNL.0000000000006241. Epub 2018 Aug 24.
PubMed 30143566Bartels B, Habets LE, Stam M, Wadman RI, Wijngaarde CA, Schoenmakers MAGC, Takken T, Hulzebos EHJ, van der Pol WL, de Groot JF. Assessment of fatigability in patients with spinal muscular atrophy: development and content validity of a set of endurance tests. BMC Neurol. 2019 Feb 9;19(1):21. doi: 10.1186/s12883-019-1244-3.
PubMed 30738436Bartels B, de Groot JF, Habets LE, Wijngaarde CA, Vink W, Stam M, Asselman FL, van Eijk RPA, van der Pol WL. Fatigability in spinal muscular atrophy: validity and reliability of endurance shuttle tests. Orphanet J Rare Dis. 2020 Mar 23;15(1):75. doi: 10.1186/s13023-020-1348-2.
PubMed 32293503Wadman RI, Wijngaarde CA, Stam M, Bartels B, Otto LAM, Lemmink HH, Schoenmakers MAGC, Cuppen I, van den Berg LH, van der Pol WL. Muscle strength and motor function throughout life in a cross-sectional cohort of 180 patients with spinal muscular atrophy types 1c-4. Eur J Neurol. 2018 Mar;25(3):512-518. doi: 10.1111/ene.13534. Epub 2018 Feb 2.
PubMed 29194869Finkel RS, Mercuri E, Darras BT, Connolly AM, Kuntz NL, Kirschner J, Chiriboga CA, Saito K, Servais L, Tizzano E, Topaloglu H, Tulinius M, Montes J, Glanzman AM, Bishop K, Zhong ZJ, Gheuens S, Bennett CF, Schneider E, Farwell W, De Vivo DC; ENDEAR Study Group. Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy. N Engl J Med. 2017 Nov 2;377(18):1723-1732. doi: 10.1056/NEJMoa1702752.
PubMed 29091570Paul GR, Gushue C, Kotha K, Shell R. The respiratory impact of novel therapies for spinal muscular atrophy. Pediatr Pulmonol. 2021 Apr;56(4):721-728. doi: 10.1002/ppul.25135. Epub 2020 Nov 2.
PubMed 33098622Heitschmidt L, Pichlmaier L, Eckerland M, Steindor M, Olivier M, Fuge I, Kolbel H, Hirtz R, Stehling F. Nusinersen does not improve lung function in a cohort of children with spinal muscular atrophy - A single-center retrospective study. Eur J Paediatr Neurol. 2021 Mar;31:88-91. doi: 10.1016/j.ejpn.2021.02.007. Epub 2021 Feb 28.
PubMed 33711791Koessler W, Wanke T, Winkler G, Nader A, Toifl K, Kurz H, Zwick H. 2 Years' experience with inspiratory muscle training in patients with neuromuscular disorders. Chest. 2001 Sep;120(3):765-9. doi: 10.1378/chest.120.3.765.
PubMed 11555507Winkler G, Zifko U, Nader A, Frank W, Zwick H, Toifl K, Wanke T. Dose-dependent effects of inspiratory muscle training in neuromuscular disorders. Muscle Nerve. 2000 Aug;23(8):1257-60. doi: 10.1002/1097-4598(200008)23:83.0.co;2-m.
PubMed 10918264
Study at a glance
From the registry record, last updated by the sponsor on 30 Nov 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Respiratory Muscle Training in Patients With Spinal Muscular Atrophy (SMA).
- ClinicalTrials.gov ID
- NCT05632666
- Acronym / sponsor ID
- RESISTANT / W.OB19-01
- Conditions
- Spinal Muscular Atrophy
- Keywords
- Spinal Muscular Atrophy, Inspiratory Muscle Training, Expiratory Muscle Training, Maximum Inspiratory Mouth Pressure, Maximum Expiratory Mouth Pressure, Respiratory Muscle Training
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 30 participants (actual)
- Lead sponsor
- UMC UtrechtUniversity, hospital or other
- Collaborators
- Princess Beatrix Muscle Foundation
- Study start
- 2 Feb 2021 (actual)
- Primary completion
- 31 Jan 2023 (estimated)
- Study completion
- 31 Jan 2023 (estimated)
- First posted
- 30 Nov 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to study respiratory muscle training in patients with Spinal Muscular Atrophy (SMA). The main questions it aims to answer are:
- Is a home-based individualized training program for the inspiratory and expiratory muscles feasible (good adherence and good acceptability)?
- Can a home-based individualized training program for the inspiratory and expiratory muscles increase the strength of these muscles? Participants will be asked to perform 10 training sessions per week, spread out over 5-7 days. Each training session consists of 30 breathing cycles through the inspiratory muscle trainer and 30 breathing cycles trough the expiratory muscle trainer.
In the first four months of the study researchers will compare two groups to see if a higher trainings load is more effective.
One group will start at a trainings load of 10% of their maximal inspiratory and expiratory muscle strength.
The other group will start at a trainings load of 30% of their maximal inspiratory and expiratory muscle strength. This group also need to adjust the trainings load based on their perceived exertion.
After four months all participants will train on a trainings load of 30% of their maximal inspiratory and expiratory muscle strength and adjust the trainings load based on their perceived exertion.
The participants will come to the hospital for lung function tests every four months for 12 months.
Detailed description
The aim of this study is to assess the feasibility and efficacy of respiratory muscle training in patients with SMA and respiratory muscle weakness. The hypothesis is that an individualized incremental home-based respiratory muscle training program will be feasible and will improve inspiratory muscle strength, expiratory muscle strength, lung function and patient reported breathing difficulties in patients with SMA.
Study setting: This study is conducted at the outpatient department of the Netherlands SMA center and the Child Development and Exercise Center at the University Medical Center Utrecht (UMCU), The Netherlands. All members of the study team, consisting of physicians, physiotherapists, lung function technicians, clinical exercise physiologists and nurses, have broad experience with SMA due to the national cohort study that is carried out in this center since 2010.
Study design: The RESISTANT study is an investigator-initiated, mono-center study consisting of two parts:
Part 1 (0-4 months): a single blinded randomized sham-controlled trial (RCT). In the first part of the study, the feasibility and efficacy of respiratory muscle training (RMT) in patients with SMA will be determined.
Before the first visit, participants will be recruited for enrollment by a research nurse. Patients who express interest in participating receive a patient information letter and an appointment with the physiotherapist. At the first visit (M0), the physiotherapist further determines whether patients are eligible for participation. After signing the informed consent form, participants are weighed and their length is determined, followed by lung function tests. If the maximum inspiratory mouth pressure (PImax) >80 centimeter of Water Column (cmH2O), participants are excluded for the study. If PImax ≤ 80 cmH2O, participants will be stratified prior to randomization based on PImax (group 1: PImax <60 cmH2O, group 2: PImax ≥60 cmH2O, 60 cmH2O was the median PImax in the group of patients used for the natural history study). Participants will be randomly allocated to the intervention or sham-control group. A variable block randomization method with allocation concealment in a centralized system will be used for randomization. The lung function analyst is blinded for treatment allocation. A data analyst will design and sign the data analysis plan in advance. The data will be analyzed according to the analysis plan by a physiotherapist who is not blinded for treatment allocation. The physiotherapists who will perform the two-weekly telephone calls are not blinded for treatment allocation. Patients will know that there are two treatment groups, and they are informed that it is not yet known which treatment is most effective.
All participants (and parents) will be instructed by a trained physiotherapist on the use of both devices at the first visit (baseline or M0). Participants are instructed to aim for 10 training sessions per week, divided over 5 to 7 days. A minimum of 6 hours in between training sessions is recommended. Per training session, the participant breathes 30 times through the POWERbreathe (inspiratory muscle training) and 30 times through the reverse Threshold® IMT (expiratory muscle training). If necessary, the participant may take a break, with a maximum of 60 seconds after 10 or 15 breaths. After each session they fill in a diary, which contains information about the load and the perceived exertion (Borg scale 0-10).
In the active treatment group, the intensity of the training is set at M0 at 30% of PImax and maximum expiratory mouth pressure (PEmax) and will be increased or decreased based on level of perceived exertion. Participants are instructed to increase the intensity with 1-5 cmH2O if they score a perceived exertion of 0-4 and decrease the intensity if they score a perceived exertion of 7-10. If they score a perceived exertion of 5 or 6, the intensity will not me adjusted. The intensity of the training in the sham-controlled group will be set at M0 at 10% of PImax and PEmax and will remain the same during the first 4 months of training.
- Inspiratory muscle trainer: For the inspiratory muscle training (IMT) the Conformité Européenne certified POWERbreathe KHP2 is used. Clinical research has shown high participant motivation and adherence to training with the POWERbreathe KHP2 thanks to the on-screen feedback. Furthermore, healthcare professionals can review participant progress by tracking up to 30 of the participants training sessions which the KHP2 is able to store. This data can be scrolled through to monitor progress. The electronic, variable, tapered flow valve ensures maximum training benefit. It is easy to use, easy to clean and training improvements can be easily monitored.
- Expiratory muscle trainer: For the expiratory muscle training (EMT) the Threshold Inspiratory Muscle Trainer (IMT) (Philips Respironics) in reverse is used. Use of the Threshold Positive Expiratory Pressure (PEP) (Philips Respironics) is one method to perform EMT. However, the maximal expiratory resistance of the Threshold PEP is limited to 20 cmH20. To overcome this limitation in expiratory resistance, the Threshold IMT will be used in reverse. This device contains, at its end, a valve closed by the positive pressure of a spring, which can be graded from 9 to 41 cmH2O and allows resistance changes by 1 cmH2O increments. The reverse Threshold IMT has a one-way spring-loaded valve, that closes during expiration and requires that participants exhale hard enough, to open the valve and let the air go out. This device provides constant pressure for expiratory muscle training, regardless of how quickly or slowly the participant breathes, and the optimal loading pressure can be adjusted, based upon the individual characteristics of the participant.
Part 2 (5-12 months): open label extension phase. In the second part of the study, the sham-control group will be provided with a supervised RMT at a therapeutic intensity of 30% of PImax and PEmax and the long-term effects of RMT on the occurrence of respiratory infections, health related quality of life and feasibility will be investigated in the active treatment and sham-controlled group.
Participants will visit our outpatient department every 4 months for 12 months after inclusion for assessment of primary and secondary outcome measures. This study is currently ongoing; the first participant was included on 2-2-2021. Study completion is expected in the first quarter of 2023.
Sample size: Based on a previous report on inspiratory muscle training in patients with neuromuscular diseases (n=27, 18 patients with Duchenne Muscular Dystrophy (DMD) and 9 patients with SMA) indicating a mean improvement in PImax of 28 cmH2O difference (SD ±26.27), a mean difference of 20 cmH2O (SD 25.0) is assumed between active and sham treated patients after 4 months. To detect this effect size with 80% power and two-sided alpha of 5%, 50 patients are needed (25 per group).
Statistical analysis: Continuous variables will be expressed as means with standard deviations or medians with interquartile ranges (whichever is more appropriate), and discrete variables will be expressed as numbers with percentages. The main efficacy population will consist of all patients being randomized and analyzed according to their original treatment allocation, irrespective of actual received treatment or follow-up (intention-to-treat). The primary comparison will be the mean difference in PImax at month 4. An ANCOVA model will be used to analyze the differences between groups adjusting for baseline PImax. Missing data in the outcomes at month 4 will be imputed by the baseline-observation-carried-forward (BOCF) approach. This will be a conservative method because expected is that patients' PImax will improve after training. For the longitudinal data, a mixed model will be used for repeated measurements including a term for visit, treatment, their interaction, and baseline PImax to account for the correlation within subjects. Similar models will be used for the secondary endpoints. The incidence of adverse events will be summarized by treatment group and in all treatment groups combined in frequency tables, coded according to the introductory guide Medical Dictionary for Regulatory Activities (MedDRA) version 21.0.
Data management: The following measures will be taken to assure the confidentiality and anonymity of the participants' data or documents collected in Castor: a) each participant will be identified in an electronic database by a unique six digit code; b) the list of participant names corresponding to the codes will be stored in a separate encrypted electronic database, safeguarded by the principal investigator; c) only study investigators will have access to the databases and examine individual data or documents; d) all logins will be recorded; e) adopt strict precautions to prevent access to the data or documents by non-authorized persons; f) the handling of data and documents will comply with the General data protection regulation (GDPR) and is further described in the Data Monitoring Plan.
Ethics, dissemination, and safety monitoring: The investigator obtains written informed consent before study participation from participants and from parents if the participant is <16 years old.
The trial is monitored by an external independent party (Julius Clinical). Because of the negligible risk classification minimal monitoring will be necessary. All participants are insured by the sponsor in case of harm due to study participation.
The study will be conducted according to the principles of the Declaration of Helsinki, adapted 19-10-2013, and in accordance with the Medical Research Involving Human Subjects Act (WMO). The code of Conduct as agreed upon 2001 by the Dutch organization of Pediatrics will be used. The study is partly done by minors, which means that in any case of resistance the test and research protocol will be terminated. Resistance means that the patient's behavior obviously differs from or is more excessive compared to participant's normal behavior. The national rules of the Dutch Association of Pediatrics for protection of minor study participants, are followed during the entire study. The results of this study will be publicly disclosed in several publications in peer reviewed scientific journals related to the topic of this study and orally in conferences concerning this theme.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- In the first four months of the study, the active treatment group will receive inspiratory muscle training starting at a therapeutic intensity of 30% of maximum inspiratory mouth pressure (PImax) and expiratory muscle training starting at a therapeutic intensity of 30% of maximum expiratory mouth pressure (PEmax). The sham-control group will receive the same training protocol but with a low (10% of PImax and PEmax) non-therapeutic intensity. After four months, the sham-control group will also be provided with a supervised RMT at a therapeutic intensity of 30% of PImax and PEmax.
| Arm | Type | Receives |
|---|---|---|
| Active treatment group | Experimental | Other: Inspiratory and expiratory muscle training at a therapeutic intensity |
| Sham-controlled group | Sham comparator | Other: Inspiratory and expiratory muscle training at a non-therapeutic intensity |
Who may qualify
- Ages
- 8 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (4 listed)
- Age ≥ 8 years;
- Respiratory muscle weakness (PImax ≤80 cmH2O (31));
- Maintenance dose (≥2 months) Spinraza® or (≥2 months) Risdiplam or no treatment;
- Given oral and written informed consent when ≥18 years old and additional informed consent by the parents or legal representative if the participant is <16 years old.
Key exclusion criteria (4 listed)
- Inability to perform respiratory and/or lung-function testing;
- Inability to understand Dutch or English;
- A history of pneumothorax or symptomatic low cardiac output syndrome;
- Treatment period < 2 months of Spinraza® or Risdiplam
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Inspiratory and expiratory muscle training at a therapeutic intensityThe active treatment group will receive inspiratory muscle training starting at a therapeutic intensity of 30% of maximum inspiratory mouth pressure (PImax) and expiratory muscle training starting at a therapeutic intensity of 30% of maximum expiratory mouth pressure (PEmax) for 4 months. In the active treatment group, the inspiratory and expiratory threshold (intensity) will be adjusted to the perceived exertion (measured with a Borg scale). | Other | Active treatment group |
| Inspiratory and expiratory muscle training at a non-therapeutic intensityThe sham-control group will receive the same training protocol as the active treatment group but with a low (10% of PImax and PEmax) and stable non-therapeutic intensity. | Other | Sham-controlled group |
Primary outcome
Maximal inspiratory mouth pressure (PImax)
Time frame: Baseline
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Maximal inspiratory mouth pressure (PImax)
Time frame: 4 months
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Maximal inspiratory mouth pressure (PImax)
Time frame: 8 months
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Maximal inspiratory mouth pressure (PImax)
Time frame: 12 months
Maximal inspiratory mouth pressure in Centimeter of Water Column (cmH2O) assessed conform the European Respiratory Society/American Thoracic Society (ERS/ATS) recommendations. Reference values of Wilson et al. 1984 will be used to calculate % of predicted.
Feasibility: adherence from baseline (M0) to 4 months visit (M4)
Time frame: From baseline (M0) to 4 months visit (M4)
The completion rate of the estimated number of training sessions over 4 months (>80% of the participants have fulfilled the prescribed treatment = good adherence). Adherence will be monitored by a patient diary, the data saved in the POWERbreathe KHP2 and, two weekly telephone- or video calls by a physiotherapist.
Feasibility: adherence from 4 months (M4) to 8 months visit (M8)
Time frame: From 4 months (M4) to 8 months visit (M8)
The completion rate of the estimated number of training sessions over 4 months (>80% of the participants have fulfilled the prescribed treatment = good adherence). Adherence will be monitored by a patient diary, the data saved in the POWERbreathe KHP2 and, two weekly telephone- or video calls by a physiotherapist.
Feasibility: adherence from 8 months (M8) to 12 months visit (M12)
Time frame: From 8 months (M8) to 12 months visit (M12)
The completion rate of the estimated number of training sessions over 4 months (>80% of the participants have fulfilled the prescribed treatment = good adherence). Adherence will be monitored by a patient diary, the data saved in the POWERbreathe KHP2 and, two weekly telephone- or video calls by a physiotherapist.
Feasibility: acceptability
Time frame: 4 months
The willingness to continue the training (>5 = good acceptability) assessed with a Borg Scale (0-10)
Feasibility: acceptability
Time frame: 8 months
The willingness to continue the training (>5 = good acceptability) assessed with a Borg Scale (0-10)
Feasibility: acceptability
Time frame: 12 months
The willingness to continue the training (>5 = good acceptability) assessed with a Borg Scale (0-10)
54 secondary outcomes
Maximal expiratory mouth pressure (PEmax)
Time frame: Baseline
Maximal expiratory mouth pressure (PEmax)
Time frame: 4 months
Maximal expiratory mouth pressure (PEmax)
Time frame: 8 months
Maximal expiratory mouth pressure (PEmax)
Time frame: 12 months
Health related quality of life
Time frame: Baseline
Health related quality of life
Time frame: 4 months
Health related quality of life
Time frame: 8 months
Health related quality of life
Time frame: 12 months
Forced vital capacity (FVC)
Time frame: Baseline
Forced vital capacity (FVC)
Time frame: 4 months
Forced vital capacity (FVC)
Time frame: 8 months
Forced vital capacity (FVC)
Time frame: 12 months
Slow vital capacity (SVC)
Time frame: Baseline
Slow vital capacity (SVC)
Time frame: 4 months
Slow vital capacity (SVC)
Time frame: 8 months
Slow vital capacity (SVC)
Time frame: 12 months
Peak expiratory flow (PEF)
Time frame: Baseline
Peak expiratory flow (PEF)
Time frame: 4 months
Peak expiratory flow (PEF)
Time frame: 8 months
Peak expiratory flow (PEF)
Time frame: 12 months
Forced expiratory volume in 1 second (FEV1)
Time frame: Baseline
Forced expiratory volume in 1 second (FEV1)
Time frame: 4 months
Forced expiratory volume in 1 second (FEV1)
Time frame: 8 months
Forced expiratory volume in 1 second (FEV1)
Time frame: 12 months
Peak cough flow (PCF)
Time frame: Baseline
Peak cough flow (PCF)
Time frame: 4 months
Peak cough flow (PCF)
Time frame: 8 months
Peak cough flow (PCF)
Time frame: 12 months
Sniff Nasal Inspiratory Pressure (SNIP)
Time frame: Baseline
Sniff Nasal Inspiratory Pressure (SNIP)
Time frame: 4 months
Sniff Nasal Inspiratory Pressure (SNIP)
Time frame: 8 months
Sniff Nasal Inspiratory Pressure (SNIP)
Time frame: 12 months
Mouth occlusion pressure at 100ms (P0.1)
Time frame: Baseline
Mouth occlusion pressure at 100ms (P0.1)
Time frame: 4 months
Mouth occlusion pressure at 100ms (P0.1)
Time frame: 8 months
Mouth occlusion pressure at 100ms (P0.1)
Time frame: 12 months
P0.1/PImax
Time frame: Baseline
P0.1/PImax
Time frame: 4 months
P0.1/PImax
Time frame: 8 months
P0.1/PImax
Time frame: 12 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Nov 2022.
- Background: PubMed 23115209Wadman RI, Vrancken AF, van den Berg LH, van der Pol WL. Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3. Neurology. 2012 Nov 13;79(20):2050-5. doi: 10.1212/WNL.0b013e3182749eca. Epub 2012 Oct 31.
- Background: PubMed 28392274Finkel RS, Sejersen T, Mercuri E; ENMC SMA Workshop Study Group. 218th ENMC International Workshop:: Revisiting the consensus on standards of care in SMA Naarden, The Netherlands, 19-21 February 2016. Neuromuscul Disord. 2017 Jun;27(6):596-605. doi: 10.1016/j.nmd.2017.02.014. Epub 2017 Mar 2. No abstract available.
- Background: PubMed 18572081Lunn MR, Wang CH. Spinal muscular atrophy. Lancet. 2008 Jun 21;371(9630):2120-33. doi: 10.1016/S0140-6736(08)60921-6.
- Background: PubMed 28676062Verhaart IEC, Robertson A, Wilson IJ, Aartsma-Rus A, Cameron S, Jones CC, Cook SF, Lochmuller H. Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature review. Orphanet J Rare Dis. 2017 Jul 4;12(1):124. doi: 10.1186/s13023-017-0671-8.
- Background: PubMed 17761659Wang CH, Finkel RS, Bertini ES, Schroth M, Simonds A, Wong B, Aloysius A, Morrison L, Main M, Crawford TO, Trela A; Participants of the International Conference on SMA Standard of Care. Consensus statement for standard of care in spinal muscular atrophy. J Child Neurol. 2007 Aug;22(8):1027-49. doi: 10.1177/0883073807305788.
- Background: PubMed 30061431Stam M, Wadman RI, Wijngaarde CA, Bartels B, Asselman FL, Otto LAM, Goedee HS, Habets LE, de Groot JF, Schoenmakers MAGC, Cuppen I, van den Berg LH, van der Pol WL. Protocol for a phase II, monocentre, double-blind, placebo-controlled, cross-over trial to assess efficacy of pyridostigmine in patients with spinal muscular atrophy types 2-4 (SPACE trial). BMJ Open. 2018 Jul 30;8(7):e019932. doi: 10.1136/bmjopen-2017-019932.
- Background: PubMed 30143566Mongiovi P, Dilek N, Garland C, Hunter M, Kissel JT, Luebbe E, McDermott MP, Johnson N, Heatwole C. Patient Reported Impact of Symptoms in Spinal Muscular Atrophy (PRISM-SMA). Neurology. 2018 Sep 25;91(13):e1206-e1214. doi: 10.1212/WNL.0000000000006241. Epub 2018 Aug 24.
- Background: PubMed 30738436Bartels B, Habets LE, Stam M, Wadman RI, Wijngaarde CA, Schoenmakers MAGC, Takken T, Hulzebos EHJ, van der Pol WL, de Groot JF. Assessment of fatigability in patients with spinal muscular atrophy: development and content validity of a set of endurance tests. BMC Neurol. 2019 Feb 9;19(1):21. doi: 10.1186/s12883-019-1244-3.
- Background: PubMed 32293503Bartels B, de Groot JF, Habets LE, Wijngaarde CA, Vink W, Stam M, Asselman FL, van Eijk RPA, van der Pol WL. Fatigability in spinal muscular atrophy: validity and reliability of endurance shuttle tests. Orphanet J Rare Dis. 2020 Mar 23;15(1):75. doi: 10.1186/s13023-020-1348-2.
- Background: PubMed 29194869Wadman RI, Wijngaarde CA, Stam M, Bartels B, Otto LAM, Lemmink HH, Schoenmakers MAGC, Cuppen I, van den Berg LH, van der Pol WL. Muscle strength and motor function throughout life in a cross-sectional cohort of 180 patients with spinal muscular atrophy types 1c-4. Eur J Neurol. 2018 Mar;25(3):512-518. doi: 10.1111/ene.13534. Epub 2018 Feb 2.
- Background: PubMed 29091570Finkel RS, Mercuri E, Darras BT, Connolly AM, Kuntz NL, Kirschner J, Chiriboga CA, Saito K, Servais L, Tizzano E, Topaloglu H, Tulinius M, Montes J, Glanzman AM, Bishop K, Zhong ZJ, Gheuens S, Bennett CF, Schneider E, Farwell W, De Vivo DC; ENDEAR Study Group. Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy. N Engl J Med. 2017 Nov 2;377(18):1723-1732. doi: 10.1056/NEJMoa1702752.
- Background: PubMed 33098622Paul GR, Gushue C, Kotha K, Shell R. The respiratory impact of novel therapies for spinal muscular atrophy. Pediatr Pulmonol. 2021 Apr;56(4):721-728. doi: 10.1002/ppul.25135. Epub 2020 Nov 2.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Erik Hulzebos, Dr principal investigator
UMC Utrecht
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Inspiratory and expiratory muscle training at a therapeutic intensity and Inspiratory and expiratory muscle training at a non-therapeutic intensity in people with Spinal Muscular Atrophy, run by UMC Utrecht at 1 site in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 30 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Maximal inspiratory mouth pressure (PImax) (time frame: Baseline). The study lists 10 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05632666, which also lists 24 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Nov 2022.