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NCT03252873 Clinical Trial

THE FACTORS AFFECTING THE ADHERENCE TO THE PULMONARY REHABILITATION PROGRAM IN COPD

COPD Clinical Trial

Official title:
INVESTIGATION THE FACTORS AFFECTING THE ADHERENCE TO THE OUTPATIENT PULMONARY REHABILITATION PROGRAM IN COPD

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03252873
Other study ID # IzmirKCU2
Secondary ID
Status Completed
Phase N/A
First received August 15, 2017
Last updated August 16, 2017
Start date January 2013
Est. completion date May 2017

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

Clinical Trial Summary

Investigators will compare the factors affecting the adherence to the outpatient pulmonary rehabilitation program in COPD patients

Description:

Patients were referred to the Pulmonary Rehabilitation Unit and were recommended to participate in the exercise program by a team of experts included in this study.

Demographic and clinical characteristics of patients were recorded before the pulmonary rehabilitation program. All cases were evaluated by pulmonary function test, arterial blood gas analysis, six minute walking test, MMRC Dyspnea Scale. Causes that prevented program adaptation of those who did not participate in the program or who left the program were questioned. Patients completing the eight-week PR program will compare with those who did not complete the program or who did not start the program at the recommended time.

Recruitment information / eligibility
Status Completed
Enrollment 359
Est. completion date May 2017
Est. primary completion date May 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: COPD Patients referred to the outpatient pulmonary rehabilitation unit -

Exclusion Criteria: To be unvolunteer

Study Design

Related Conditions & MeSH terms

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 Respiratory Function Test FEV1 (%) FEV1 /FVC TLCO (%) FEV1 (%), FEV1 /FVC, TLCO (%) 15 minutes
Secondary Blood Gase Analysis PAO2, PaCO2, SaO2 5 minutes
Secondary Six minute walk test walking distance 10 minutes
Secondary MMRC Dyspnea Scale 1-5 5 minutes
Secondary SGRQ Questionnaire Symptom-Activity-Impact- Total 20 minutes
Secondary HAD Questionnaire Anxiety- Depression score 15 minutes
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