About this trial
Chronic Obstructive Pulmonary Disease (COPD) affects approximately 16 million Americans and is characterized by recurrent exacerbations that lead to 1.5 million Emergency Department visits and 700,000 hospitalizations annually. Pulmonary rehabilitation (PR) is a structured program of exercise and self-management support that has been proven to relieve shortness of breath and increase quality of life when initiated after an exacerbation, but unfortunately, few eligible patients participate. This project will compare the effectiveness of two novel strategies - one involving video narratives of other patients telling their story of how they overcame challenges and completed PR, the other involving telephonic peer coaching with an individual with lived experience - to enhanced usual care, and to each other, at increasing patient participation in PR after an exacerbation.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
40 years or older
Received treatment for COPD exacerbation in either inpatient or outpatient setting
Referred for pulmonary rehabilitation
Ability to understand and communicate in English
Disqualifiers
Unwilling to attend PR
Not eligible for PR based on spirometry or other clinical contraindications as determined by PR staff
Currently enrolled in, or completion of 12 or more sessions of PR in the past
Comfort measures only or Hospice care
Trial design
Parallel
Treatments tested in this trial
Telephonic Peer Coaching
BehavioralTelephonic Peer Coaching from an individual with lived experience with COPD and Pulmonary Rehabilitation trained in motivational interviewing
Storytelling
BehavioralVideo narratives of an individual with lived experience with COPD and Pulmonary Rehabilitation describing their journey through Pulmonary Rehabilitation
Treatment groups
Trial outcomes
Primary outcomes
Number of Pulmonary Rehabilitation (PR) sessions: Completion of ≥6 PR sessions within 6 months of randomization
Secondary outcomes
Any attendance (yes/no) at PR within 6 months of randomization.
Total number of PR sessions completed within 6 months of randomization.
Time to first PR session attended
Other outcomes
Change in Modified Medical Research Council (mMRC) dyspnea scale from randomization to 6 months
Change in Clinical COPD Questionnaire (CCQ) from randomization to 6 months
Change in Hospital Anxiety and Depression Scale (HADS) from randomization to 6 months
Activation (Self Efficacy for Managing Chronic Diseases 6)
Sponsors and contacts
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Baystate Medical Center
Lead sponsor
University of Michigan
Collaborator
University of Massachusetts, Worcester
Collaborator
COPD Foundation
Collaborator
National Heart, Lung, and Blood Institute (NHLBI)
Collaborator