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Combined Effects of Ba-Duan-Jin Based Deep Breathing Exercises and Forced Expiratory Technique - Trial NCT06332417

Access comprehensive clinical trial information for NCT06332417 through Pure Global AI's free database. This phase not specified trial is sponsored by Riphah International University and is currently Recruiting. The study focuses on Chronic Obstructive Pulmonary Disease. Target enrollment is 68 participants.

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NCT06332417
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Trial Details
ClinicalTrials.gov โ€ข NCT06332417
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Combined Effects of Ba-Duan-Jin Based Deep Breathing Exercises and Forced Expiratory Technique
Combined Effects of Ba-Duan-Jin Based Deep Breathing Exercises and Forced Expiratory Technique in Patients With Chronic Obstructive Pulmonary Disease

Study Focus

Ba-Duan-Jin Based Deep Breathing Exercises

Interventional

other

Sponsor & Location

Riphah International University

Lahore, Pakistan

Timeline & Enrollment

N/A

Feb 29, 2024

Jun 15, 2024

68 participants

Primary Outcome

36-Item Short Form Survey (SF-36),FEV1/FVC ratio,Exercise Tolerance : 6 minute walk test,Forced vital capacity (FVC),Forced expiratory volume (FEV1)

Summary

This study will be a randomized control trial. A total of 68 patients will be recruited and
 randomly assign to the experimental group or the control group in a 1:1 ratio. Participants
 in the experimental group will receive a 8-week Ba-duan jin exercise training intervention
 along with Forced Expiratory Technique at least 3 days a week and 30 minutes a day, while
 participants in the control group will be only given Forced Expiratory intervention and will
 be told to maintain their original lifestyle for 8 weeks along with standard COPD treatment.

ICD-10 Classifications

Other chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease, unspecified
Other specified chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease with acute exacerbation, unspecified
Chronic obstructive pulmonary disease with acute lower respiratory infection

Data Source

ClinicalTrials.gov

NCT06332417

Non-Device Trial