Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07269262

SUPPORT-T in Patients With Progressive Pulmonary Fibrosis and Their Caregivers

Led by Medical University of South Carolina · Updated on 2026-02-02

170

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This pilot randomized controlled trial evaluates the feasibility, acceptability, and accessibility of SUPPORT-T, a digitally delivered palliative care intervention for patients with Progressive Pulmonary Fibrosis (PPF) and their caregivers. The intervention includes a 9-week digital application guided by a nurse interventionist and quarterly virtual support groups over one year. Participants will be recruited from rural South Carolina and urban New York City. The study compares SUPPORT-T to Enhanced Usual Care and aims to inform a future multi-site trial.

CONDITIONS

Official Title

SUPPORT-T in Patients With Progressive Pulmonary Fibrosis and Their Caregivers

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years and older
  • Confirmed diagnosis of Progressive Pulmonary Fibrosis
  • Able to speak and understand English or Spanish
  • Caregivers must be adults 18 years or older
  • Caregivers must be designated by the patient as the main provider of emotional, financial, or physical support
  • Caregivers must be able to speak and understand English
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

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Research Team

K

Kathleen Lindell, PhD, RN, ATSF, FAAN

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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