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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05397275
Other study ID # osmaniye korkut ata university
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2021
Est. completion date October 1, 2021

Study information

Verified date May 2022
Source Osmaniye Korkut Ata University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim: This study was conducted to determine the effect of progressive muscle relaxation and breathing exercise on sleep quality and exercise self-efficacy in chronic obstructive pulmonary patients. Methods: This study was conducted as a randomized controlled experimental study. The study was conducted with 64 chronic obstructive pulmonary patients, where 36 of them were in the intervention group and 34 in the control group. Data of the study were collected using the descriptive information form, the Pittsburgh Sleep Quality Index, and the Exercise Self-Regulatory Efficacy Scale (Ex-SRES) for patients with COPD. Results: When the total scores pertaining to the sleep quality index and exercise self-efficacy of the individuals in the intervention and control groups were compared, it was found that there were statistically significant differences in the intervention group compared to the control group (p < 0.05). Keywords: Exercise Self-Regulatory Efficacy, sleep quality in patients with COPD, PGE along with breathing exercises, pulmonary rehabilitation


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date October 1, 2021
Est. primary completion date July 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - were to be 18 years of age or older - not using sleeping pills - verbally stating that they have moderate and severe sleep disorders. Exclusion Criteria: - having any lung disease other than COPD - having cardiological problems (heart failure, uncontrollable hypertension, history of angina and myocardial infarction, heart valve problems), psychotic disorder, - inability to communicate verbally and having hearing problems.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
progressive muscle relaxation+breathe exercises
progressive muscle relaxation+breathe exercises
breathe exercises
breathe exercises

Locations

Country Name City State
Turkey Aksaray University Aksaray

Sponsors (1)

Lead Sponsor Collaborator
Osmaniye Korkut Ata University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary progressive muscle relaxation exercises changes sleep quality and exercise self-efficacy. Sleep quality will be assessed using the Pittsburgh Sleep Quality Index as an pre- test and 4 weeks later as a post-test test. 1 mounth
Secondary progressive muscle relaxation exercises with breathing exercise changes sleep quality and exercise self-efficacy. Sleep quality will be assessed using the Pittsburgh Sleep Quality Index as an pre-test and 4 weeks later as a post-test.
.The Exercise Self-Regulatory Efficacy Scale will be used as a pre-test and after 4 weeks as a post-test to measure the exercise capacity of COPD patients.
1 mounth
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