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Neuromuscular DisordersNCT02833168

Screening Questionnaire for Respiratory Muscle Weakness and Sleep-disordered Breathing in Neuromuscular Disorders

An observational study of Neuromuscular Disorders, run by Universität Münster at 2 sites in Germany.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

It is the aim of this project to develop and validate a German language screening questionnaire for symptoms of respiratory muscle weakness and sleep-disordered breathing (SDB) in patients with neuromuscular disorders. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Neuromuscular Disorders
What is being tested?
patient-filled questionnaires and spiromanometry
Type of treatment
Medical device
How many people
90 participants
Where
2 sitesGermany
Study dates
Apr 2016to Dec 2016
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 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with neuromuscular disorders, newly diagnosed obstructive sleep apnea syndrome or sleep disorders other than sleep-related breathing disorders (30 patients in each group)

Who may be able to join

  • proven neuromuscular disease known to be potentially associated with diaphragmatic weakness (group 1)
  • newly diagnosed obstructive sleep apnea with an apnea hypopnea index > 15/h total sleep time (group 2)
  • newly diagnosed narcolepsy, hypersomnia, insomnia or parasomnia in the absence of any sleep-related breathing disorder (group 3)
  • availability of recent diagnostic sleep studies including polysomnography and transcutaneous capnography

Who cannot join

  • ongoing CPAP oder non-invasive ventilation
  • inability to participate in study procedures
  • severe lung disease

Trial locations and contacts

2 sites in 1 country.

Germany2 sites, 2 recruiting
  • University Hospital Münster, Department of Sleep Medicine and Neuromuscular Disorders

    Münster, 48149

    Matthias Boentert, MD, +49-251-83 ext. 44458, matthias.boentert@ukmuenster.de

    Peter Young, MD, +49-251-83 ext. 48196, peter.young@ukmuenster.de

    Recruiting
  • Bethanien Hospital

    Solingen, 42699

    Winfried Randerath, MD, +49-212 630 ext. 0, Winfried.Randerath@klinik-bethanien.de

    Wiebke Dohrn, MD, +49-212 630 ext. 0, Wiebke.Dohrn@klinik-bethanien.de

    Recruiting

Other trials in Germany

About this study

Official title: Validation of a German Language Screening Questionnaire for Symptoms of Respiratory Muscle Weakness and Sleep-disordered Breathing in Patients With Neuromuscular Disorders

It is the aim of this project to develop and validate a German language screening questionnaire for symptoms of respiratory muscle weakness and sleep-disordered breathing (SDB) in patients with neuromuscular disorders.

Read the detailed description

SDB is a promiment clinical feature of various neuromuscular disorders including amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), and myopathies such as myotonic dystrophy type 1, Pompe disease, and limb-girdle muscular dystrophies (LGMD). In ALS, SMA, LGMD and Pompe disease, SDB is usually caused by nocturnal alveolar hypoventilaton due to diaphragmatic weakness which manifests first during sleep and REM sleep in particular. SDB usually leads to sleep disruption, non-restorative sleep and daytime symptoms including morning headache, hypersomnolence, and increased neuromuscular fatigue. In patients with severe diaphragmatic involvement both symptoms of SDB and potential complications of respiratory muscle weakness substantially add to overall disease burden of the disease and decrease life span. Diagnosis of SDB is established by means of sleep studies which should ideally comprise polysomnography (PSG) and transcutaneous capnography. PSG with capnometry is time-consuming, expensive and not readily available for patients or referring physicians, respectively. For this reason it is desirable to thoroughly screen patients with neuromuscular disease for symptoms of SDB and respiratory muscle weakness. Results from a validated screening questionnaire could be used as an adjunctive to pulmonary function testing or spirometry results in order to identify patients in whom sleep studies should be performed. In addition, a screening questionnaire would facilitate early recognition of patients with SDB, enabling treating physicians to take appropriate steps to establish the diagnosis and to initiate non-invasive ventilation as early as possible.

Until now, there is no validated German language screening questionnaire for symptoms of respiratory muscle weakness and SDB. Steier et al. published an English language questionnaire which was validated as a screening tool in 33 patients with very different neuromuscular disorders which were predominantly neurogenic (Steier et al. 2011). In this study, SDB was defined by an apnea hypopnea index above 5 per hour. Nocturnal oxygen saturation and CO2 monitoring were not taken into account at all. In addition the questionnaire does not systematically cover sleep-related symptoms of SDB in detail (such as sleep disruption and morning headache) which have to be separated from daytime symptoms such as dyspnea or orthopnea, respectively.

Thus, the current project aims to correlate comprehensively generated items of a screening questionnaire with sleep study results including capnography alongside with respiratory muscle testing in patients with neuromuscular disorders. As control subjects, patients with newly diagnosed obstructive sleep apnea syndrome and sleep disorders other than sleep-related breathing disorders are enrolled in the study.

Being tested
patient-filled questionnaires, spiromanometry
Keywords
Neuromuscular disorders, Sleep disordered breathing, Dyspnea
Medical subject headings
Neuromuscular Diseases, Sleep Apnea Syndromes, Dyspnea

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • patient-filled questionnairesOther

    All patients answer selected questionnaires on sleep-related symptoms, sleep quality, daytime performance, and health-related quality of life.

  • spiromanometryDevice

    Measurement of forced vital capacity, maximum inspiratory pressure and maximum expiratory pressure

Study groups in NCT02833168
Study groupRoleWhat they receive
1Patients with proven neuromuscular disorders known to be potentially associated with significant diaphragmatic weakness, e. g. ALS, myotonic dystrophy type 1, limb-girdle muscular dystrophy, Duchenne and Becker muscular dystrophy. Patients already receiving home ventilatory support will not be included in the study.
Receives: Other: patient-filled questionnaires; Device: spiromanometry
2Patient with proven obstructive sleep apnea syndrome prior to CPAP initiation.
Receives: Other: patient-filled questionnaires; Device: spiromanometry
3Patients with sleep disorders other than sleep-related breathing disorders, e. g. narcolepsy, hypersomnia, parasomnia or sleep-related movement disorders.
Receives: Other: patient-filled questionnaires; Device: spiromanometry

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Nocturnal hypercapnia tcCO2

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Jul 2016 (estimated)
  2. Study startApr 2016
  3. Primary completionDec 2016 (estimated)
  4. Study completionDec 2016 (estimated)

Resources

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
Case-control
Time perspective
Prospective
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02833168
Sponsor's protocol ID
KSN_2016_1_MB
Status last verified
Jul 2016
First submitted
12 Jul 2016
Last updated
14 Jul 2016
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Neuromuscular Disorders, run by Universität Münster at 2 sites in Germany.

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 3 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 14 Jul 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Germany. 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?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Matthias Boentert, MD (+49-251-83 ext. 44458, matthias.boentert@ukmuenster.de), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Nocturnal hypercapnia tcCO2 (time frame: 1 day). 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 14 Jul 2016.

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