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

Status

Unknown

Intervention / Treatment

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

      • Geneva, Switzerland, 1211
        • Geneva University Hospitals

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
8 weeks of CPAP therapy

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.

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

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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