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

Overview

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

Full Title of Study: “Has Pulmonary Rehabilitation a Positive Impact on Sleep Quality in Patients Suffering From Chronic Obstructive Pulmonary Disease?”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: August 31, 2022

Detailed 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.

Interventions

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

Arms, Groups and Cohorts

  • COPD patients following a pulmonary rehabilitation program
    • COPD patients following a pulmonary rehabilitation program

Clinical Trial Outcome Measures

Primary Measures

  • sleep efficiency
    • Time Frame: 3 +/- 2 months
    • sleep efficiency assessed by actigraphy

Secondary Measures

  • steps
    • Time Frame: 3 +/- 2 months
    • number of steps walked daily assessed by actigraphy

Participating in This Clinical Trial

Inclusion Criteria

  • COPD patients – able to walk and cycle Exclusion Criteria:

  • Shift work – orthopedic diseases of limbs

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 90 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Centre Hospitalier Universitaire Saint Pierre
  • Provider of Information About this Clinical Study
    • Principal Investigator: Marie Bruyneel, Chef de Clinique – Centre Hospitalier Universitaire Saint Pierre

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