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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04744220
Other study ID # 10840098-604.01.01-E.19408
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 25, 2020
Est. completion date December 30, 2022

Study information

Verified date October 2022
Source Istanbul Medipol University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 30, 2022
Est. primary completion date November 20, 2022
Accepts healthy volunteers No
Gender All
Age group 30 Years to 55 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Other:
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. The patients will start with breathing exercises, then relaxation exercises, warm-up exercises, asanas (posture exercises) and finally the yoga training program will be completed with deep relaxation technique.

Locations

Country Name City State
Turkey Istanbul Medipol University Hospital Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul Medipol University Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Respiratory Function Test A spirometer will be used to evaluate the lung function of individuals. It will be expressed as a percentage of the expected values by age, height, body weight and gender. Before and after treatment( 8 week )
Other Quality of Life Assessment Quality of life, St. George's Respiratory Questionnaire (SGRQ). SGRQ is a health-related quality of life questionnaire that questions a total of 50 items under 3 main components: symptoms (8 items), activity (16 items) and effects of disease (26 items). The symptoms component includes the frequency and duration of symptoms such as cough, sputum, shortness of breath, wheezing.
The activity component relates to physical activities that are restricted due to shortness of breath. It includes factors such as the effects component of the disease, the drugs used and its side effects, the individual's expectations for health and the discomfort they face in daily life. The total score is between 0-100. The higher the score, the lower the quality of life
Before and after treatment (8 week)
Other Evaluation of Functional Capacity Individuals' functional capacity will be evaluated with the six-minute walking test (6MWT). During the 6MWT, individuals are asked to walk in a straight corridor of 30 meters as fast as possible, at their own walking pace in standard directions.
At the end of the test, the walking distance is recorded in meters.
Before and after treatment (8 week)
Other Assessment of Sleep Quality Pittsburgh Sleep Quality Index (PSQI) will be used to evaluate the sleep quality of the individuals participating in our study before and after the 8-week study period.
PSQI is a test that plays a role in determining sleep quality and sleep-related disorders in the last month. It is a scale consisting of 19 self-report items, a total of 24 questions with a score range of 0-21, and the remaining five questions must be answered by a roommate or a spouse. It is a test that evaluates a wide variety of areas related to sleep quality, including components, sleep time, delays in falling asleep, the frequency and severity of sleep-related problems, and the impact of poor sleep on an individual's work.
Before and after treatment (8 week)
Primary Patient Follow-up Form 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. Baseline
Secondary Dyspnea Assessment 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.
Before and after treatment (8 week)
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