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Clinical Trials/NCT04704310
NCT04704310
Completed
Not Applicable

Enhancing Exercise Training for Adults With COPD: The Roles of Peers and Functional Tasks

McGill University1 site in 1 country4 target enrollmentJanuary 27, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pulmonary Disease, Chronic Obstructive
Sponsor
McGill University
Enrollment
4
Locations
1
Primary Endpoint
Participant Adherence
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This study aims to find a new way to get individuals living with COPD to become and stay active during and after an exercise intervention. In this study, individuals living with COPD will participate in an online exercise intervention. The exercises included in this intervention are based in individuals' activities of daily living. Additionally, during this intervention, individuals with COPD will participate in peer support sessions and will be taught and encouraged to discuss eight behaviour change techniques that have been shown to help support increased participation in physical activity and/or exercise. The goal of this study is to test out this new protocol and determine if it is feasible to recreate on a larger scale and if it is acceptable for the COPD community.

Registry
clinicaltrials.gov
Start Date
January 27, 2021
End Date
April 15, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shane Norman Sweet

Associate Professor

McGill University

Eligibility Criteria

Inclusion Criteria

  • Individuals must be at least 18 years of age, have no diagnosed cognitive impairment, have a COPD diagnosis (any stage), be medically able to participate in exercise (confirmed by healthcare professional in the past 2 years), have access to a computer with a camera and internet, and speak English or French.

Exclusion Criteria

  • less than 18 years of age, diagnosed with a cognitive impairment, not diagnosed with COPD by a medical professional, unable to participate in exercise or unconfirmed in the past 2 years from a medical professional, no access to a computer and internet.

Outcomes

Primary Outcomes

Participant Adherence

Time Frame: 8 weeks

Intervention adherence will be measured be taking attendance for each session (2 x 8 weeks = 16 sessions). Intervention feasibility as an indicator of success will be an overall program adherence rate of 70% (approximately 11 sessions attended by all participants, respectively)

Goal Participation

Time Frame: 8 weeks

Participant goal participation will be measured by improvement in initial goals set at the beginning of the study using the Canadian Occupation Performance Measures (COPM). Success will be determined by calculating individuals change score on their satisfaction with their performance in their target areas. A change score of 2 on an item is said to represent significant change (Law et al., 2000). A change score of at least 2 on 50% of items (dependent on personal goals) for 70% of participants will be the indicator of success.

Participant Engagement

Time Frame: 8 weeks

Participant engagement will be measured by counting the number of unique topics brought up by each participant. The indicator of success will be that each participant initiates 1 topic of conversation in 70% of session (initiates 11 conversations during program)

Secondary Outcomes

  • 3-minute step test(Baseline, immediately after intervention (9 weeks after baseline))
  • Motivation for Exercise Questionnaire(Baseline, immediately after intervention (9 weeks after baseline))
  • Godin Leisure Time Physical Activity Questionnaire(Baseline, immediately after intervention (9 weeks after baseline))
  • The Satisfaction with Life Questionnaire(Baseline, immediately after intervention (9 weeks after baseline))
  • Timed "Up & Go" test(Baseline, immediately after intervention (9 weeks after baseline))
  • 1-minute sit-to-stand test(Baseline, immediately after intervention (9 weeks after baseline))
  • The Psychological Need Satisfaction in Exercise scale(Baseline, immediately after intervention (9 weeks after baseline))
  • Handgrip Test(Baseline, immediately after intervention (9 weeks after baseline))
  • Six-minute walk test(Baseline, immediately after intervention (9 weeks after baseline))
  • Borg Scale - Dyspnea(Baseline, immediately after intervention (9 weeks after baseline))

Study Sites (1)

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