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

  • STATUS
    Recruiting
  • End date
    Dec 17, 2023
  • participants needed
    80
  • sponsor
    Mayo Clinic
Updated on 17 March 2022

Summary

The purpose of this study is to gather information on the effectiveness of a home-based pulmonary rehabilitation program with health coaching and tele-monitoring for improving patient-reported respiratory-related quality of life and physical activity in patients with fibrotic Interstitial Lung Diseases (f-ILD).

Description

The home-based pulmonary rehabilitation program involves using a computer tablet paired with a pulse oximeter and activity tracker. Gentle upper body exercises, walking and a breathing practice are completed by following along on the computer tablet. Weekly check-in calls by telephone will be provided by a Health Coach to assess clinical status and monitor progress. The exercise portion of the program lasts 12 weeks. There are questionnaires and a research grade activity tracker measuring baseline and post-intervention findings at the end of 12-week period.

Details
Condition Fibrotic Interstitial Lung Disease
Treatment Home-based pulmonary rehabilitation
Clinical Study IdentifierNCT05130034
SponsorMayo Clinic
Last Modified on17 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Diagnosis of idiopathic pulmonary fibrosis (IPF) or other fibrotic interstitial lung disease, with a minimum of > 10% fibrosis on computed tomography imaging
Clinically meaningful breathlessness: modified Medical Research Council (mMRC) dyspnea score >1

Exclusion Criteria

Inability to walk (orthopedic/neurologic/cardiac limitation causing immobility)
Cognitive impairment or inability to understand and follow instructions
Traditional PR completed within 3 months of study recruitment
Hospice or end-of-life care at the time of screening
Acute exacerbation at the time of screening
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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