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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03227341
Other study ID # KCU123
Secondary ID
Status Completed
Phase N/A
First received July 20, 2017
Last updated July 21, 2017
Start date January 1, 2013
Est. completion date January 1, 2017

Study information

Verified date July 2017
Source Izmir Katip Celebi University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators compared the effectiveness of pulmonary rehabilitation program on asthma control in patients with uncontrolled and partially controlled asthma.


Description:

Asthma treatment is not only medical, it also requires a comprehensive care including nonpharmacological treatment. Pulmonary rehabilitation represents the most important part of the comprehensive care. The investigators aimed to evaluate the efficacy of pulmonary rehabilitation in patients with uncontrolled and partially controlled asthma.

Asthma patients referred to pulmonary rehabilitation (PR) unit were classified according to asthma control test; as partially controlled patients (Group 1), and as uncontrolled patients (Group 2). All patients received of a 8 week pulmonary rehabilitation program. Asthma control tests, pulmonary function tests, arterial blood gases analysis, dyspnea perception, quality of life, exercise capacity, anxiety and depression assessments were performed before and after pulmonary rehabilitation.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date January 1, 2017
Est. primary completion date January 1, 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Asthmatic patients referred from the outpatient clinic to Pulmonary Rehabilitation unit was confirmed according to GINA guidelines

Exclusion Criteria:

- If the initial diagnosis cannot be confirmed, the patient excluded from the study

- Patients were under medical treatment of -6 months and considered clinically stable.

- Patients with cardiovascular, other lung diseases (pneumoconiosis, pulmonary tuberculosis, interstitial lung disease), or musculoskeletal diseases that would impair exercise training were excluded from the study.

- Also subjects with lack of motivation, poor compliance (not attending the program more than 2 times) or having transport problems were excluded from the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
8 week exercise program including breathing exercises consisted of pursed-lip breathing, diaphragmatic breathing and thoracic expansion exercises, relaxation and stretching exercises, upper and lower extremity muscle strength training, and aerobic exercises. In addition, bronchial hygiene techniques and dyspnea-reducing positions

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Izmir Katip Celebi University

Outcome

Type Measure Description Time frame Safety issue
Primary Asthma control test score A test measured the control of asthma 4 weeks
Secondary Exercise capacity Six minute walk test 6 minute
Secondary Dyspnea MMRC Dyspnea Scale 1 year
Secondary Quality of Life St. George Respiratory Questionnaire 1 year
Secondary Pulmonary Function Test FEV1, FVC, DLCO 1 hour
Secondary Arterial Blood Gas PaO2, PaCO2, SaO2 1 hour
Secondary Anxiety and Depression Hospital Anxiety and Depression Scale 1 week
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