Home-based Pulmonary Rehabilitation and Health Coaching in Patients With Fibrotic Interstitial Lung Disease

Description

The purpose of this clinical trial is to determine the impact of a home-based pulmonary rehabilitation program with health coaching on patient-reported respiratory-related quality of life and physical activity, as compared to usual care in patients with fibrotic interstitial lung disease.

Conditions

Lung Fibrosis, Lung Interstitial Disease

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Study Overview

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Study Details

Study overview

The purpose of this clinical trial is to determine the impact of a home-based pulmonary rehabilitation program with health coaching on patient-reported respiratory-related quality of life and physical activity, as compared to usual care in patients with fibrotic interstitial lung disease.

Home-based Pulmonary Rehabilitation and Health Coaching in Patients With Fibrotic Interstitial Lung Disease: A Prospective Pragmatic Randomized Waitlist-Controlled Trial

Home-based Pulmonary Rehabilitation and Health Coaching in Patients With Fibrotic Interstitial Lung Disease

Condition
Lung Fibrosis
Intervention / Treatment

-

Contacts and Locations

Scottsdale

Mayo Clinic in Arizona, Scottsdale, Arizona, United States, 85259

Jacksonville

Mayo Clinic in Florida, Jacksonville, Florida, United States, 32224

Rochester

Mayo Clinic in Rochester, Rochester, Minnesota, United States, 55905

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * F-ILD diagnosis, any disease subtype, active or prior medical treatment
  • * \>10% fibrosis on CT imaging
  • * mMRC dyspnea score \>1
  • * All racial or ethnic categories, including non-English speakers (professional translators will be engaged to support screening, enrollment, and study participation)
  • * Inability to walk (orthopedic/neurologic/cardiac limitation causing immobility)
  • * Cognitive impairment or inability to understand and follow instructions
  • * Traditional center-based PR completed within 3 months of initial study recruitment
  • * Transition to hospice or end-of-life care at the time of screening
  • * Acute exacerbation at the time of screening

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Mayo Clinic,

Teng Moua, PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

2030-09-30