Actively Recruiting

Phase 3
Age: 45Years +
All Genders
NCT06932887

The Beat Pain Better Trial

Led by University of Utah · Updated on 2026-01-29

346

Participants Needed

3

Research Sites

148 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The Beat Pain Better study examines strategies to increase the reach of evidence-based interventions for persons with osteoarthritis (OA) in communities that experience disparities. The study is a hybrid type 3 effectiveness-imple-mentation trial using sequential, multiple assignment, ran¬domi¬zation to evaluate 1) two text mes¬saging strat¬egies to reach persons with OA and enroll them in physical activity counseling provided by physical therapists; and 2) two strat¬egies to engage enrolled persons in the Walk with Ease (WWE) intervention for sustained self-management.

CONDITIONS

Official Title

The Beat Pain Better Trial

Who Can Participate

Age: 45Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 45 or older
  • Visited a participating medical clinic within the past 6 months
  • Osteoarthritis diagnosis related to lower extremity and/or spine recorded in the past 6 months
  • Has a working cell phone able to receive calls and text messages
Not Eligible

You will not qualify if you...

  • Unable to participate in a regular walking program, defined as being unable to walk for at least five minutes even with an assistive device
  • Medical reasons that prevent participation in physical activity
  • Unable to communicate in either Spanish or English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

University of Utah

Salt Lake City, Utah, United States, 84106

Not Yet Recruiting

2

Association for Utah Community Health

Salt Lake City, Utah, United States, 84107

Actively Recruiting

3

Vamos Health

West Valley City, Utah, United States, 84120

Actively Recruiting

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Research Team

J

Julie Fritz, PhD, PT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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