Improving Participation in Pulmonary Rehabilitation Through Peer Support and Storytelling

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorBaystate Medical Center

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Telephonic Peer Coaching

    Behavioral

    Telephonic Peer Coaching from an individual with lived experience with COPD and Pulmonary Rehabilitation trained in motivational interviewing

  • Storytelling

    Behavioral

    Video narratives of an individual with lived experience with COPD and Pulmonary Rehabilitation describing their journey through Pulmonary Rehabilitation

Treatment groups

305 Participants
are divided into 3 treatment groups
Group A: Enhanced usual careNo intervention 0 interventions
Group B: Enhanced usual care + StorytellingActive comparator 1 intervention
Group C: Enhanced usual care + Peer supportActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Number of Pulmonary Rehabilitation (PR) sessions: Completion of ≥6 PR sessions within 6 months of randomization

Time frame
6 months

Secondary outcomes

1

Any attendance (yes/no) at PR within 6 months of randomization.

Time frame
6 months
2

Total number of PR sessions completed within 6 months of randomization.

Time frame
6 months
3

Time to first PR session attended

Time frame
6 months

Other outcomes

1

Change in Modified Medical Research Council (mMRC) dyspnea scale from randomization to 6 months

Time frame
6 months
2

Change in Clinical COPD Questionnaire (CCQ) from randomization to 6 months

Time frame
6 months
3

Change in Hospital Anxiety and Depression Scale (HADS) from randomization to 6 months

Time frame
6 months
4

Activation (Self Efficacy for Managing Chronic Diseases 6)

Time frame
6 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

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