Fracture of Proximal End of HumerusPERFoRMNCT05390463
Feasibility of the PERformance Guided Fracture Rehablitation Method-protocol
An observational study of Fracture of Proximal End of Humerus and Fracture of Distal End of Radius, run by Zuyderland Medisch Centrum at 1 site in Netherlands.
Trial summary
Introduction: The scientific support for prescribed rehabilitation programs for upper extremity fractures is scarce, early mobilization has previously been shown to benefit the speed of recovery at the activity and participation level. Read more about this study
- Who is it for?
- Ages 18 to 70 years
- Conditions the study is for
- Fracture of Proximal End of Humerus, Fracture of Distal End of Radius, Upper Extremity Fracture
- What is being tested?
- PERformance guided Fracture Rehablitation Method (PERFoRM) protocol.
- How many people
- 20 participants
- Where
- 1 siteNetherlands
- Study dates
- 24 Apr 2022to 28 Nov 2023
- How long will I take part?
- 6 Months
- Phase
- Observational
- 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 18 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Study population: Patients with surgically treated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures) treated within the MDTU (Multi Disciplinary Trauma Unit) of the Zuyderland MC in Heerlen are included in this study.
Who may be able to join
- The inclusion criteria:
- Patients with a surgically treated (osteosynthesis) proximal humeral or distal radius fracture
- Patients aged 18 to 70 years
- Patients with a premorbid level with at least independent living and independence in ADL and/or HDL.
- Patients are able to come to the Rehabilitation outpatient clinic of the Zuyderland MC in Heerlen for treatment
- Patients are sufficiently instructable with regard to communication/language (NL/English)
Show all 15Show fewer
- The exclusion criteria:
- Multiple fractures to 1 limb
- Pathological fractures
- Complications such as trophic dysregulation/CRPS at the time of inclusion
- Extensive concomitant neurovascular injury at the time of inclusion
- Cognitive problems with regard to learnability and instructability
- Influencing psychological problems or active substance use (with the exception of injury/trauma-related (movement) anxiety, event PTSD)
- Influencing other problems/comorbidities to upper extremity such as neuromuscular disorders and anatomic anomalies
- The subject is not prepared to conform to the informed consent
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Feasibility of the PERformance Guided Fracture Rehablitation Method (PERFoRM) Protocol for Periarticular Upper Extremity Fractures
Introduction: The scientific support for prescribed rehabilitation programs for upper extremity fractures is scarce, early mobilization has previously been shown to benefit the speed of recovery at the activity and participation level. Different (inter)national protocols for fracture rehabilitation of the upper extremity are not very specific with regard to the content of (para)medical treatment. The above underlines the need for a clearly defined and practically feasible treatment method.
That is why the PERformance guided Fracture Rehablitation Method (PERForRM) protocol was drawn up, in which the treatment method is clearly described in a structured and protocol-based manner. The ultimate goal of the PERformance guided Fracture Rehablitation Method (PERFoRM) protocol is to optimize recovery, with maximum recovery of activity and participation level in upper extremity fractures. Expert opinion/empiricism was used during the writing of the protocol, partly arising from the earlier development of a protocol for the lower extremity. The approach according to the PERForRM protocol does not focus on the time-contingent load on the fracture, but rather on the functional use of the extremity, whereby the quality of movement is paramount. The PERForRM protocol proposes a "gold standard" in the form of milestones for describing the quality of movement of the upper extremity for (para)medics.
Read more
Method:
The aim of this pilot study is to test the manageability/feasibility of this protocol in clinical practice in patients with peri-articular fractures of the upper extremity (proximal humeral and distal radius fractures). It also describes the recovery in the area of the ICF domains and the complications that occurred when applying the PERForRM protocol. The inclusion period consists of 3 months, with a follow-up of 6 months. The manageability is measured by means of a questionnaire that is administered to the practitioners (2x during the study period). The data analysis will mainly have a descriptive character
Read the detailed description
Research question:
Question 1: How has the feasibility of the PERFORM protocol been applied in patients with peri-articular fractures of the upper extremity (operated proximal humeral and distal radius fractures)? Question 2a: How is the recovery on the different ICF domains after applying the PERFORM protocol in patients with peri-articular fractures of the upper extremity (proximal humeral and distal radius fractures) compared to results already described in the literature with regard to recovery (semi-structured treatment / protocols) after related fractures? Question 2b: Is the number of complications occurring when applying the PERFORM protocol equal to the results already described in the literature with regard to recovery (semi-structured treatment / protocols) after the relevant fractures?
Hypothesis:
Question 1: The PERForRM protocol can be used by both physicians and paramedics in the trauma rehabilitation chain. Experiences of physicians and paramedics show that the protocol is useful and applicable within the patient population (patients with peri-articular fractures of the upper extremity (operated proximal humeral and distal radius fractures)).
Question 2a: Patients with peri-articular fractures of the upper extremity treated with the PERFORM protocol show comparable or faster recovery in the different ICF domains compared to patients with peri-articular fractures of the upper extremity (proximal humerus). - and distal radius fractures) treated with a different post-treatment protocol (often diverse and semi- or only globally structured) as described in the literature.
Question 2b: A comparable number of complications occur in the study population and recovery in the different ICF domains is as fast or faster compared to results from the literature already described (Quick-DASH, JAMAR, NPRS, RAND-36).
Goal:
The aim of this study is to gain insight into the feasibility of the PERFORM protocol in patients with peri-articular fractures of the upper extremity (operated proximal humeral and distal radius fractures). The patients receive care-as-usual, but structured and recorded according to the PERForRM protocol. In addition, the aim of this study is to document the recovery of the patient population at the ICF level with a structured follow-up treatment according to the PERFORM protocol.
Method:
The manageability of the PERForRM protocol is investigated in a prospective, observational study design. Patients with upper extremity fractures are included post-operatively and treated according to the PERFORM protocol for 3 months. Measurement moments are 0-2, 6, 12 weeks and 6 months after the fracture. The paramedical treatment will last 3 months, after which, depending on the performance level at that time, an advice will be issued regarding aftercare.
The inclusion will take place within the MDTU (MultiDisciplinary Trauma Unit) of the Zuyderland MC in Heerlen by the specialties surgery and orthopedics and the associated (trauma) surgeons and orthopaedists. The application of the paramedical treatment will take place within the Rehabilitation Department of the Zuyderland MC at the Heerlen location.
Study population:
Patients with operated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures) who are undergoing treatment within the MDTU (Multi Disciplinary Trauma Unit) of the Zuyderland MC in Heerlen are included in this study.
Number of intended subjects:
Given the limited number of intended subjects and the heterogeneity of the group and the lack of a normal distribution of the descriptive prospective pilot study, a sample size calculation is not realistic. In view of the feasibility of the pilot study within the Rehabilitation Department, an estimate was made with regard to the inclusion number of a maximum of 30 subjects. The maximum number of 30 subjects was chosen because of the practical feasibility and treatment capacity of the rehabilitation outpatient clinic.
Data collection:
Research question 1: Two qualitative measurements were performed to test the practicality of the PERForRM protocol. The feasibility of the PERForRM protocol is recorded twice via a standardized questionnaire with the practitioner (start and end of the pilot).
Research question 2 (2a/2b): PAG = pt ass guide; AIG = aims ident guide; TEG = treatment evaluation guide; Milestones = standardized list of skills to be achieved; (quick-)DASH = disab arm should hand; JAMAR = JAMAR hand dynamometer; NPRS = num pain rating scale; RAND-36 = research and develop-36; general health condition.
Collecting data:
The medical information is collected by the doctors involved in this study The paramedical information is collected by the paramedics involved.
Data Inspection:
Given the predominantly descriptive nature of this pilot study and the existing experience with treatment as described in the protocol, no extreme qualitative or quantitative values are expected. If this is the case, the pilot should be able to detect these kinds of effects. If missing values arise in the questionnaires, reminders are sent repeatedly to encourage people to provide missing data.
Testing for normal distribution:
Since this study is a pilot study, as a result of which the number of participants is so low and the patients with their fractures are so heterogeneous, it is expected that the data will not be distributed according to a normal distribution. This is tested by means of the Shapiro-Wilk test.
Descriptive statistics:
For the normally distributed data, the mean +/-SD will be reported and students' t-test will be used for comparisons. For non-parametric data, we will report the median +/- interquartile range (IQR) and use the Mann Whitney U tests. The descriptive statistics of the results of the survey data are presented in tables. From there, the ordinal values will be used to calculate means, median, and dispersion. The nominal values will be shown in percentages of the whole.
(Interim) analyses: After completion of the rehabilitation, the data is processed and further descriptive. At the end of the 3-month follow-up, data are completed and added anonymously to the complete data set. Given the predominantly descriptive nature of the study, we do not expect extensive analyses, this will be limited to: Discriptives, T-Test (comparison T0, T1, T2, T3).
Coding and Interpreting:
The experiences of the (para)medics will be collected in the form of a questionnaire. The research group collects these experiences, which are then displayed anonymously. Subsequently, the qualitative data is coded and categorized and interpreted by means of a code tree.
Software:
Software that is used for registering data is data manager and for analyzing the results Excel and/or SPSS.
Data management:
- Location: the research data is initially collected in the patient file. From the patient file, this data is extracted to data manager and, if necessary, exported to Excel/SPSS.
- Retention of data: The data associated with this study will be kept for 15 years.
- Security of data: the research data as stated in the patient file are only accessible to the (para)medics involved. Data-manager is accessible to all members of the research team.
- Coding: the coding takes place after the patient has completed the informed consent. Numbers from 1 to 100 are assigned to the patient's hospital identification number and are saved in a new Excel file. This will be done for one of the researchers.
- Code key: The code key is stored on a server at Medisch Centrum Zuyderland. Only listed researchers have access to the code key.
Protection of privacy
- The privacy of the participants is protected from the basic agreements for the use of the patient file. Furthermore, no data is recorded in places other than the patient file or data manager.
- Sharing data: The data is not shared with institutions or persons outside Zuyderland. Results of the pilot in general, in the form of a scientific presentation/publication, are shared with institutions/persons outside Zuyderland. However, these are not micro-level data, but macro-level data that provide answers to the research questions.
- Conditions
- Fracture of Proximal End of Humerus, Fracture of Distal End of Radius, Upper Extremity Fracture, Upper Limb Fracture
- Being tested
- PERformance guided Fracture Rehablitation Method (PERFoRM) protocol.
- Keywords
- Fracture, Upper extremity, Radius, Humerus, Surgery, Rehabilitation, Surgical fixation, Protocol
- Medical subject headings
- Fractures, Bone
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PERformance guided Fracture Rehablitation Method (PERFoRM) protocol.Other
A structured rehabilitation protocol for surgically treated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures).
| Study group | Role | What they receive |
|---|---|---|
| PERFoRM | Patients with surgically treated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures) undergoing treatment within the MDTU (Multi Disciplinary Trauma Unit) of the Zuyderland MC in Heerlen are included in this study. Receives: Other: PERformance guided Fracture Rehablitation Method (PERFoRM) protocol. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Feasibility of the PERFoRM-protocol at starting point of the study: qualitative assessment through standardized questionnaire.
Feasibility of the PERFoRM-protocol: qualitative assessment through standardized questionnaire (questionnaire composed by investigator).
Measured: at starting point of the study (before the first inclusion); at 0 months.
Feasibility of the PERFoRM-protocol at 6 months after the starting point of the study: qualitative assessment through standardized questionnaire.
Feasibility of the PERFoRM-protocol: qualitative assessment through standardized questionnaire (questionnaire composed by investigator).
Measured: 6 months after above-mentioned starting point of the study.
Secondary outcomes (4)
Change of rate of disability of (affected) arm-shoulder-hand.
Measurement of change in rate of disability of (affected) arm-shoulder-hand, through (Quick-) DASH; Disability Arm Shoulder Hand - questionnaire.
Scoring: range 0-100. Score 0: no limitations in functioning. Score 100: high limitations in functioning.
Measured: Change between immediate phase (0-2 weeks) post-surgery, 6 weeks post-surgery, 3 months post-surgery, 6 months post surgery.
Change in handstrength of affected limb.
Measurement of change in handstrength of affected limb, through hand-held-dynamometer.
Reference table handstrength:
- Men: 0kg (lowest strength) - 64kg (highest strength);
- Women: 0kg (lowest strength) - 39kg (highest strength).
Measured: Change between immediate phase (0-2 weeks) post-surgery, 6 weeks post-surgery, 3 months post-surgery, 6 months post surgery.
Change in pain of affected limb.
Measurement of change in pain of affected limb, through Numeric Pain Rating Scale (NPRS).
Scoring: range 0-10. Score 0: no pain. Score 10: worst pain ever.
Measured: Change between immediate phase (0-2 weeks) post-surgery, 6 weeks post-surgery, 3 months post-surgery, 6 months post surgery.
Change in general health status.
Measurement of change in general health status, through Research and develop-36; general health status (RAND-36) - questionnaire.
Scoring: range 0-100. Higher scores present better general health status.
Measured: Change between immediate phase (0-2 weeks) post-surgery, 3 months post-surgery, 6 months post surgery.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 May 2022
- Study start24 Apr 2022
- Primary completion28 Nov 2023
- Study completion28 Nov 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Fracture of Proximal End of HumerusStudies of the same condition, open and under way.
- 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 20 participants (actual)
- Target duration
- 6 Months
Sponsor and investigators
- Lead sponsor
- Zuyderland Medisch Centrum
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- MPM Dremmen, MD, Principal investigator, Zuyderland Medisch Centrum
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05390463
- Sponsor's protocol ID
- Z2021143
- Acronym
- PERFoRM
- Status last verified
- Jul 2024
- First submitted
- 22 Mar 2022
- Last updated
- 26 Jul 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Jul 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Feasibility of the PERformance Guided Fracture Rehablitation Method (PERFoRM) Protocol for Periarticular Upper Extremity Fractures
- ClinicalTrials.gov ID
- NCT05390463
- Acronym / sponsor ID
- PERFoRM / Z2021143
- Conditions
- Fracture of Proximal End of Humerus, Fracture of Distal End of Radius, Upper Extremity Fracture, Upper Limb Fracture
- Keywords
- Fracture, Upper extremity, Radius, Humerus, Surgery, Rehabilitation, Surgical fixation, Protocol
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Zuyderland Medisch CentrumUniversity, hospital or other
- Study start
- 24 Apr 2022 (actual)
- Primary completion
- 28 Nov 2023 (actual)
- Study completion
- 28 Nov 2023 (actual)
- First posted
- 25 May 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.
Introduction: The scientific support for prescribed rehabilitation programs for upper extremity fractures is scarce, early mobilization has previously been shown to benefit the speed of recovery at the activity and participation level. Different (inter)national protocols for fracture rehabilitation of the upper extremity are not very specific with regard to the content of (para)medical treatment. The above underlines the need for a clearly defined and practically feasible treatment method.
That is why the PERformance guided Fracture Rehablitation Method (PERForRM) protocol was drawn up, in which the treatment method is clearly described in a structured and protocol-based manner. The ultimate goal of the PERformance guided Fracture Rehablitation Method (PERFoRM) protocol is to optimize recovery, with maximum recovery of activity and participation level in upper extremity fractures. Expert opinion/empiricism was used during the writing of the protocol, partly arising from the earlier development of a protocol for the lower extremity. The approach according to the PERForRM protocol does not focus on the time-contingent load on the fracture, but rather on the functional use of the extremity, whereby the quality of movement is paramount. The PERForRM protocol proposes a "gold standard" in the form of milestones for describing the quality of movement of the upper extremity for (para)medics.
Method:
The aim of this pilot study is to test the manageability/feasibility of this protocol in clinical practice in patients with peri-articular fractures of the upper extremity (proximal humeral and distal radius fractures). It also describes the recovery in the area of the ICF domains and the complications that occurred when applying the PERForRM protocol. The inclusion period consists of 3 months, with a follow-up of 6 months. The manageability is measured by means of a questionnaire that is administered to the practitioners (2x during the study period). The data analysis will mainly have a descriptive character
Detailed description
Research question:
Question 1: How has the feasibility of the PERFORM protocol been applied in patients with peri-articular fractures of the upper extremity (operated proximal humeral and distal radius fractures)? Question 2a: How is the recovery on the different ICF domains after applying the PERFORM protocol in patients with peri-articular fractures of the upper extremity (proximal humeral and distal radius fractures) compared to results already described in the literature with regard to recovery (semi-structured treatment / protocols) after related fractures? Question 2b: Is the number of complications occurring when applying the PERFORM protocol equal to the results already described in the literature with regard to recovery (semi-structured treatment / protocols) after the relevant fractures?
Hypothesis:
Question 1: The PERForRM protocol can be used by both physicians and paramedics in the trauma rehabilitation chain. Experiences of physicians and paramedics show that the protocol is useful and applicable within the patient population (patients with peri-articular fractures of the upper extremity (operated proximal humeral and distal radius fractures)).
Question 2a: Patients with peri-articular fractures of the upper extremity treated with the PERFORM protocol show comparable or faster recovery in the different ICF domains compared to patients with peri-articular fractures of the upper extremity (proximal humerus). - and distal radius fractures) treated with a different post-treatment protocol (often diverse and semi- or only globally structured) as described in the literature.
Question 2b: A comparable number of complications occur in the study population and recovery in the different ICF domains is as fast or faster compared to results from the literature already described (Quick-DASH, JAMAR, NPRS, RAND-36).
Goal:
The aim of this study is to gain insight into the feasibility of the PERFORM protocol in patients with peri-articular fractures of the upper extremity (operated proximal humeral and distal radius fractures). The patients receive care-as-usual, but structured and recorded according to the PERForRM protocol. In addition, the aim of this study is to document the recovery of the patient population at the ICF level with a structured follow-up treatment according to the PERFORM protocol.
Method:
The manageability of the PERForRM protocol is investigated in a prospective, observational study design. Patients with upper extremity fractures are included post-operatively and treated according to the PERFORM protocol for 3 months. Measurement moments are 0-2, 6, 12 weeks and 6 months after the fracture. The paramedical treatment will last 3 months, after which, depending on the performance level at that time, an advice will be issued regarding aftercare.
The inclusion will take place within the MDTU (MultiDisciplinary Trauma Unit) of the Zuyderland MC in Heerlen by the specialties surgery and orthopedics and the associated (trauma) surgeons and orthopaedists. The application of the paramedical treatment will take place within the Rehabilitation Department of the Zuyderland MC at the Heerlen location.
Study population:
Patients with operated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures) who are undergoing treatment within the MDTU (Multi Disciplinary Trauma Unit) of the Zuyderland MC in Heerlen are included in this study.
Number of intended subjects:
Given the limited number of intended subjects and the heterogeneity of the group and the lack of a normal distribution of the descriptive prospective pilot study, a sample size calculation is not realistic. In view of the feasibility of the pilot study within the Rehabilitation Department, an estimate was made with regard to the inclusion number of a maximum of 30 subjects. The maximum number of 30 subjects was chosen because of the practical feasibility and treatment capacity of the rehabilitation outpatient clinic.
Data collection:
Research question 1: Two qualitative measurements were performed to test the practicality of the PERForRM protocol. The feasibility of the PERForRM protocol is recorded twice via a standardized questionnaire with the practitioner (start and end of the pilot).
Research question 2 (2a/2b): PAG = pt ass guide; AIG = aims ident guide; TEG = treatment evaluation guide; Milestones = standardized list of skills to be achieved; (quick-)DASH = disab arm should hand; JAMAR = JAMAR hand dynamometer; NPRS = num pain rating scale; RAND-36 = research and develop-36; general health condition.
Collecting data:
The medical information is collected by the doctors involved in this study The paramedical information is collected by the paramedics involved.
Data Inspection:
Given the predominantly descriptive nature of this pilot study and the existing experience with treatment as described in the protocol, no extreme qualitative or quantitative values are expected. If this is the case, the pilot should be able to detect these kinds of effects. If missing values arise in the questionnaires, reminders are sent repeatedly to encourage people to provide missing data.
Testing for normal distribution:
Since this study is a pilot study, as a result of which the number of participants is so low and the patients with their fractures are so heterogeneous, it is expected that the data will not be distributed according to a normal distribution. This is tested by means of the Shapiro-Wilk test.
Descriptive statistics:
For the normally distributed data, the mean +/-SD will be reported and students' t-test will be used for comparisons. For non-parametric data, we will report the median +/- interquartile range (IQR) and use the Mann Whitney U tests. The descriptive statistics of the results of the survey data are presented in tables. From there, the ordinal values will be used to calculate means, median, and dispersion. The nominal values will be shown in percentages of the whole.
(Interim) analyses: After completion of the rehabilitation, the data is processed and further descriptive. At the end of the 3-month follow-up, data are completed and added anonymously to the complete data set. Given the predominantly descriptive nature of the study, we do not expect extensive analyses, this will be limited to: Discriptives, T-Test (comparison T0, T1, T2, T3).
Coding and Interpreting:
The experiences of the (para)medics will be collected in the form of a questionnaire. The research group collects these experiences, which are then displayed anonymously. Subsequently, the qualitative data is coded and categorized and interpreted by means of a code tree.
Software:
Software that is used for registering data is data manager and for analyzing the results Excel and/or SPSS.
Data management:
- Location: the research data is initially collected in the patient file. From the patient file, this data is extracted to data manager and, if necessary, exported to Excel/SPSS.
- Retention of data: The data associated with this study will be kept for 15 years.
- Security of data: the research data as stated in the patient file are only accessible to the (para)medics involved. Data-manager is accessible to all members of the research team.
- Coding: the coding takes place after the patient has completed the informed consent. Numbers from 1 to 100 are assigned to the patient's hospital identification number and are saved in a new Excel file. This will be done for one of the researchers.
- Code key: The code key is stored on a server at Medisch Centrum Zuyderland. Only listed researchers have access to the code key.
Protection of privacy
- The privacy of the participants is protected from the basic agreements for the use of the patient file. Furthermore, no data is recorded in places other than the patient file or data manager.
- Sharing data: The data is not shared with institutions or persons outside Zuyderland. Results of the pilot in general, in the form of a scientific presentation/publication, are shared with institutions/persons outside Zuyderland. However, these are not micro-level data, but macro-level data that provide answers to the research questions.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 6 Months
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| PERFoRM | – | Other: PERformance guided Fracture Rehablitation Method (PERFoRM) protocol.Patients with surgically treated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures) undergoing treatment within the MDTU (Multi Disciplinary Trauma Unit) of the Zuyderland MC in Heerlen are included in this study. |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Study population: Patients with surgically treated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures) treated within the MDTU (Multi Disciplinary Trauma Unit) of the Zuyderland MC in Heerlen are included in this study.
Key inclusion criteria (15 listed)
- Patients with a surgically treated (osteosynthesis) proximal humeral or distal radius fracture
- Patients aged 18 to 70 years
- Patients with a premorbid level with at least independent living and independence in ADL and/or HDL.
- Patients are able to come to the Rehabilitation outpatient clinic of the Zuyderland MC in Heerlen for treatment
- Patients are sufficiently instructable with regard to communication/language (NL/English)
Key exclusion criteria (0 listed)
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 |
|---|---|---|
| PERformance guided Fracture Rehablitation Method (PERFoRM) protocol.A structured rehabilitation protocol for surgically treated peri-articular fractures of the upper extremity (proximal humerus and distal radius fractures). | Other | PERFoRM |
Primary outcome
Feasibility of the PERFoRM-protocol at starting point of the study: qualitative assessment through standardized questionnaire.
Time frame: at starting point of the study (before the first inclusion); at 0 months.
Feasibility of the PERFoRM-protocol: qualitative assessment through standardized questionnaire (questionnaire composed by investigator).
Feasibility of the PERFoRM-protocol at 6 months after the starting point of the study: qualitative assessment through standardized questionnaire.
Time frame: 6 months after above-mentioned starting point of the study.
Feasibility of the PERFoRM-protocol: qualitative assessment through standardized questionnaire (questionnaire composed by investigator).
4 secondary outcomes
Change of rate of disability of (affected) arm-shoulder-hand.
Time frame: Change between immediate phase (0-2 weeks) post-surgery, 6 weeks post-surgery, 3 months post-surgery, 6 months post surgery.
Change in handstrength of affected limb.
Time frame: Change between immediate phase (0-2 weeks) post-surgery, 6 weeks post-surgery, 3 months post-surgery, 6 months post surgery.
Change in pain of affected limb.
Time frame: Change between immediate phase (0-2 weeks) post-surgery, 6 weeks post-surgery, 3 months post-surgery, 6 months post surgery.
Change in general health status.
Time frame: Change between immediate phase (0-2 weeks) post-surgery, 3 months post-surgery, 6 months post surgery.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Jul 2024.
- 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.
MPM Dremmen, MD principal investigator
Zuyderland Medisch Centrum
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Fracture of Proximal End of Humerus and Fracture of Distal End of Radius, run by Zuyderland Medisch Centrum 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 15 inclusion and 0 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: finished, as of the sponsor's last update on 26 Jul 2024. 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. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Feasibility of the PERFoRM-protocol at starting point of the study: qualitative assessment through standardized questionnaire. (time frame: at starting point of the study (before the first inclusion); at 0 months.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 26 Jul 2024.