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NCT02159664 Clinical Trial

Influence of Didgeridoo Practice on UA Obstruction Levels in Moderate OSA

Sleep Apnea Clinical Trial

Official title:
Influence of Didgeridoo Practice on Upper Airways Obstruction Levels in Moderate Obstructive Sleep Apnea Patients

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02159664
Other study ID # AK/14-03-25/4354
Secondary ID
Status Terminated
Phase N/A
First received June 6, 2014
Last updated September 8, 2017
Start date December 2014
Est. completion date March 2016

Study information
Verified date September 2017
Source Centre Hospitalier Universitaire Saint Pierre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Didgeridoo practice has been shown to improve OSA severity. The aim of our study is to assess the changes in upper airways obstruction levels before and after Didgeridoo practice in moderate OSA patients.

Description:

Didgeridoo practice has been shown to improve Obstructive Sleep Apnea (OSA) severity. The aim of our study is to assess the changes in upper airways obstruction levels, evaluated by sleep endoscopy, before and after 3 months of Didgeridoo practice in moderate non obese OSA patients. Severity of OSA will also be documented by polysomnography.

Recruitment information / eligibility
Status Terminated
Enrollment 4
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- moderate OSA, non obese

Exclusion Criteria:

- not willing play didgeridoo age<18 significant lung, cardiac disease neuromuscular disease psychiatric disorders drugs with influence on respiratory drive

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• didgeridoo practice
instrument lessons, 1X/w and daily practice, 20 min /d

Locations
Country Name City State
Belgium CHU St Pierre Brussels

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire Saint Pierre

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Other subjective sleep quality and sleepiness assessed by questionnaires 3 months
Primary upper airways obstruction levels assessed by drug-induced sleep endoscopy 3 months
Secondary apnea-hypopnea index assessed by polysomnography 3 months
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