- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02061046
To Study the Impact of CPAP on Gait Parameters in OSA Patients (OSA_Gait)
November 30, 2015 updated by: Gilles Allali, University Hospital, Geneva
Impact of the CPAP on Gait in OSA Patients
To study the impact of CPAP therapy on gait in patients with obstructive sleep apnea syndrome.
Study Overview
Detailed Description
To study the impact of CPAP therapy on gait velocity and temproral gait in patients with obstructive sleep apnea syndrome using the SMTEC system.
Patients will be assessed before and 8 weeks after CPAP therapy.
Study Type
Observational
Enrollment (Actual)
35
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Geneva, Switzerland, 1211
- Geneva University Hospitals
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
OSA patients without any prior treatment
Description
Inclusion Criteria:
- OSA patients newly diagnosed
Exclusion Criteria:
- acute medical illness in the past months
- neurological and psychiatric diseases
- orthopaedic, rheumatologic or any sensory conditions affecting normal walking
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
On CPAP therapy
OSA patients assessed before and after 8 weeks of CPAP therapy
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8 weeks of CPAP therapy
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Gait parameters: gait velocity [m/s]
Time Frame: 8 weeks
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gilles Allali, MD/PhD, University Hospital, Geneva
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2009
Primary Completion (Actual)
August 1, 2009
Study Completion (Anticipated)
May 1, 2018
Study Registration Dates
First Submitted
February 7, 2014
First Submitted That Met QC Criteria
February 10, 2014
First Posted (Estimate)
February 12, 2014
Study Record Updates
Last Update Posted (Estimate)
December 2, 2015
Last Update Submitted That Met QC Criteria
November 30, 2015
Last Verified
November 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PRD 10-II-7
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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