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NCT02455206 Clinical Trial

Counseling During Pulmonary Rehabilitation

COPD Clinical Trial

Official title:
Effect of Counseling During Pulmonary Rehabilitation on Self-determined Motivation Towards Physical Activity in Patients With Chronic Obstructive Pulmonary Disease

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02455206
Other study ID # KEK-ZH-Nr. 2015-0179
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2015
Est. completion date February 2020

Study information
Verified date April 2021
Source Zurich University of Applied Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to investigate if a physical activity counseling program during pulmonary rehabilitation increases the physical activity level in daily life in patients with Chronic Obstructive Pulmonary Disease.

Description:

Participants performed a 12 weeks outpatient pulmonary rehab (PR) according to guidelines. Participants allocated to intervention received PR plus physical activity (PA) counselling. PA counselling was performed using "motivational interviewing" techniques and was provided by two experiences physiotherapists independant to the rehab team. After PR and three months follow-up was evaluated if PA counselling during PR increases PA elvel (primary outcome: steps per day) in daily life. Furthermore, individual, semi-structured interviews were performed in a subgroup of participants in order to gain more detailed information about barriers and enablers of participation in daily-life activities. Participants were invited to two interviews, one right after PR the other after 3 months follow up. A content analysis was performed.

Recruitment information / eligibility
Status Completed
Enrollment 43
Est. completion date February 2020
Est. primary completion date February 2020
Accepts healthy volunteers No
Gender All
Age group 40 Years to 90 Years
Eligibility Inclusion Criteria: - confirmed COPD (GOLD stages B-D) according to GOLD-guidelines Exclusion Criteria: - Mental or physical disability (mini-mental score <20) precluding informed consent or compliance with the protocol - morphine medication - Primary diagnosis of heart failure - Uncontrolled arrhythmias causing symptoms or hemodynamic compromise - Severe co-morbidity (acute coronary syndrome, unstable angina terminal renal failure, concomitant pulmonary embolism, very severe pneumonia: CURB65>3) - Severe untreated arterial hypertension at rest (> 200 mm Hg systolic, > 120 mm Hg diastolic)

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• physical activity counseling
5 face-to-face sessions a 30 minutes during 12 weeks pulmonary rehabilitation program.
• Usual care

Locations
Country Name City State
Switzerland Kantonsspital Winterthur

Sponsors (3)
Lead Sponsor Collaborator
Zurich University of Applied Sciences Kantonsspital Winterthur KSW, Schweizer Lungenliga

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary number of steps per day 6 months
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