RECRUITING

Improving Participation in Pulmonary Rehabilitation Through Peer Support and Storytelling

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Improving Participation in Pulmonary Rehabilitation Through Peer Support and Storytelling

Quick Facts

Study Start:2023-02-24
Study Completion:2026-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05399056

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:40 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 40 years or older
  2. * Received treatment for COPD exacerbation in either inpatient or outpatient setting
  3. * Referred for pulmonary rehabilitation
  4. * Ability to understand and communicate in English
  5. * Willingness to participate in calls with peer coach and to view storytelling videos
  6. * Working phone
  1. * Unwilling to attend PR
  2. * Not eligible for PR based on spirometry or other clinical contraindications as determined by PR staff
  3. * Currently enrolled in, or completion of 12 or more sessions of PR in the past
  4. * Comfort measures only or Hospice care
  5. * Resident of long-term care facility
  6. * Unable or unwilling to give informed consent

Contacts and Locations

Study Contact

Rajashree Kotejoshyer, ScD
CONTACT
978-761-8709
Rajashree.Kotejoshyer@baystatehealth.org
Jennifer Hazelton
CONTACT
978-337-0340
jennifer.hazelton@umassmed.edu

Principal Investigator

Peter Lindenauer, MD, MSc
PRINCIPAL_INVESTIGATOR
Baystate Health

Study Locations (Sites)

Baystate Health
Springfield, Massachusetts, 01199
United States

Collaborators and Investigators

Sponsor: Baystate Medical Center

  • Peter Lindenauer, MD, MSc, PRINCIPAL_INVESTIGATOR, Baystate Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-02-24
Study Completion Date2026-08-31

Study Record Updates

Study Start Date2023-02-24
Study Completion Date2026-08-31

Terms related to this study

Keywords Provided by Researchers

  • COPD
  • Pulmonary rehabilitation
  • Storytelling
  • Peer coaching
  • motivational interviewing
  • Behavioral interventions
  • chronic obstructive pulmonary disease

Additional Relevant MeSH Terms

  • Chronic Obstructive Pulmonary Disease