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NCT03314558 Clinical Trial

Has Pulmonary Rehabilitation a Positive Impact on Sleep Quality in Patients Suffering From COPD ?

COPD Clinical Trial

Official title:
Has Pulmonary Rehabilitation a Positive Impact on Sleep Quality in Patients Suffering From Chronic Obstructive Pulmonary Disease?

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03314558
Other study ID # RR2017
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 15, 2017
Est. completion date September 30, 2022

Study information
Verified date January 2023
Source Centre Hospitalier Universitaire Saint Pierre
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of our study is to assess the impact of pulmonary rehabilitation on objective sleep quality in COPD patients.

Description:

COPD patients suffer from bad sleep quality. About 27 -50% are suffering from insomnia, and respiratory related symptoms are also inducing sleep disturbances. Recently, a correlation between altered sleep quality and low activity levels have been shown in this population. In primary insomnia, it is well established that physical activity has a positive impact on sleep quality. The purpose of our study is to assess the impact of pulmonary rehabilitation on objective sleep quality in COPD patients.

Recruitment information / eligibility
Status Completed
Enrollment 31
Est. completion date September 30, 2022
Est. primary completion date August 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - COPD patients - able to walk and cycle Exclusion Criteria: - Shift work - orthopedic diseases of limbs

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• pulmonary rehabilitation
a pulmonary rehabilitation program of 30 sessions, (3X1h/ week), will be followed by the COPD patients

Locations
Country Name City State
Belgium CHu Saint 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
Primary sleep efficiency sleep efficiency assessed by actigraphy 3 +/- 2 months
Secondary steps number of steps walked daily assessed by actigraphy 3 +/- 2 months
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