Evaluation of the Effect of Yoga Training on Functional Capacity and Quality of Life in Patients With Bronchiectasis

Not Applicable

Completed

• Conditions: Bronchiectasis Adult
• Interventions: Other: Yoga Training Program (exercises)

• Registration Number: NCT04744220
• Lead Sponsor: Istanbul Medipol University Hospital

Brief Summary

Evaluation of the Effect of Yoga Training on Functional Capacity and Quality of Life in Patients with Bronchiectasis between the ages of 30-55

Detailed Description

Investigating the effect of yoga training on functional capacity and quality of life and comparing with previous studies

Study Timeline

• Study Start: 2020-11-25
• Study First Submitted: 2021-01-21
• Study First Submitted QC: 2021-02-05
• Study First Posted: 2021-02-08
• Status Verified: 2022-10
• Primary Completion: 2022-11-20
• Study Completion: 2022-12-30
• Last Update Submitted: 2023-01-09
• Last Update Posted: 2023-01-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Diagnosed with bronchiectasis
• Age 30-55
• Not having a known systemic, orthopedic or neurological disease

Exclusion Criteria

• Severe heart failure
• People who had an acute exacerbation up to three weeks ago will not be included in the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Yoga Training Group	Yoga Training Program (exercises)	Training: Before the yoga program, the patients will be informed about the bronchiectasis disease and its symptoms, as well as all the parameters used in the evaluation, tests and the content of the yoga session. During the program, the perceived fatigue intensity of the patients will be questioned with the Modified Borg Scale. Yoga Session 1-8 weeks and duration * Breathing Exercises 5 min * Instant Relaxation Technique 2 min * Warm-up Exercises 10 min * Quick Relaxation Technique 3 min * Asanas (Posture Exercises) 15 min * Alternative Breathing Exercises 10 min * Deep Relaxation Technique 3 min

Primary Outcome Measures

Name	Time	Method
Patient Follow-up Form	Baseline	The demographic characteristics, physical characteristics such as age, height and body weight of the individuals included in the study and their education status will be recorded.

Secondary Outcome Measures

Name	Time	Method
Dyspnea Assessment	Before and after treatment (8 week)	Dyspnea will be assessed by the modified Medical Research Council (MMRC) dyspnea scale. Individuals will be asked to choose the statement that best describes their dyspnea level.; Scoring in MMRC varies between 0-4 points. "0 points" means that there is no dyspnea; "4 points" indicates a perception of dyspnea during basic daily life activities such as dressing.

Trial Locations

Locations (1)

Istanbul Medipol University Hospital; 🇹🇷 Istanbul, Turkey