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NCT07033897: HARP3

Adapting, Implementing and Evaluating the Effectiveness of HARP for People With Disabilities

Recruiting now NA Last updated 14 November 2025
What this trial tests

NA trial testing Adapted HARP in Disabilities Physical in 80 participants. Currently enrolling.

Timeline
20 August 2025
Primary endpoint
14 March 2028
14 March 2028

Quick facts

Lead sponsorWashington University School of Medicine
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment80
Start date20 August 2025
Primary completion14 March 2028
Estimated completion14 March 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Washington University School of Medicine

Who can join

Adults 45 to 64, any sex, with Disabilities Physical or Falls. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The Home Hazard Removal Program (HARP) is an effective fall prevention intervention program which targets home hazard identification/removal. In this study the investigators will examine the effectiveness and implementation potential of HARP, adapted for PwD. Investigators will conduct a pilot randomized control trial (RCT) to test the implementation, cost, and preliminary efficacy of an adapted version of HARP for community-dwelling PwD. The single-blinded feasibility RCT will randomize 40 participants to treatment (adapted HARP) and 40 to a waitlist control group. Data on specific types of fall hazards and resulting home modifications as well as falls and fall-related injuries (collected monthly over 12 months) and fear of falling (collected at baseline and 12 months) will inform the preliminary efficacy of adapted HARP among PwD. To ensure usefulness, relevance, and broad dissemination of findings, the investigators will adopt a "designing for implementation and dissemination" approach. The RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) framework will guide intervention adaptation, trial design, and future implementation. The Practical Robust Implementation and Sustainability Model (PRISM) guides study development by identifying multi-level contextual factors hypothesized to affect the RE-AIM outcomes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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