Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
NCT06811389

Reimagining Interventions for Support and Education in Hypersensitivity Pneumonitis

Led by Weill Medical College of Cornell University · Updated on 2025-06-18

40

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

Sponsors

W

Weill Medical College of Cornell University

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The central hypothesis is that a peer coach-delivered intervention that includes cognitive behavioral principles combined with theory-driven patient education will improve health-related quality of life (HRQOL) of patients with hypersensitivity pneumonitis (HP). The goal of this behavioral and educational intervention, RISE-HP, is to improve health-related quality of life in people who have hypersensitivity pneumonitis and assess feasibility and accessibility of this intervention. Patients with hypersensitivity pneumonitis (HP) experience uncertainty, feelings of anxiety and depression, and marked disruption to their lifestyle and home environment. Poor health-related quality of life (HRQOL) in HP is also driven in part by patients' profound lack of knowledge about the disease. Existing interventions for patients with HP do not target improvement in quality of life. Participants will complete either RISE-HP, a 10-session peer coach delivered behavioral and educational intervention to improve HRQOL in HP, or Staying Well, a 10-session general health education program.

CONDITIONS

Official Title

Reimagining Interventions for Support and Education in Hypersensitivity Pneumonitis

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have documented diagnosis of Hypersensitivity Pneumonitis by treating clinician
  • Age 18 or older
  • English Speaking
  • Willing to work with a peer coach
  • Have a working smart phone or tablet
  • Have access to the internet
  • Reside or live in the United States
  • Endorse verbal approval from treating physician to participate in patients' goal movement/physical activity
  • Baseline score on the PHQ8 of <20
Not Eligible

You will not qualify if you...

  • Does not have Hypersensitivity Pneumonitis
  • Younger than age 18
  • Severe cognitive impairment as determined by their treating physician
  • Severe depression (PHQ-8 score 60)
  • Documentation of an eating disorder, active substance use disorder, suicidality, homicidality, acute posttraumatic stress disorder, or episodes of mania or psychosis
  • Determined to be severely ill or moribund by the treating clinician

AI-Screening

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Trial Site Locations

Total: 1 location

1

Weill Cornell Medicine

New York, New York, United States, 10065

Actively Recruiting

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Research Team

A

Anna Tharakan, BS

CONTACT

A

Alicia Morris

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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