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Clinical Trials/NCT07330492
NCT07330492Active, not recruitingNot Applicable

Randomized Controlled Trial of a Nudge Intervention for Common Musculoskeletal Conditions

University of Texas at Austin1 site in 1 country144 target enrollmentStarted: January 10, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
144
Locations
1
Primary Endpoint
Pre-visit enthusiasm for additional care

Study Overview

Brief Summary

The goal of this clinical trial is to learn if a brief, reassuring pre-visit message affects patients' expectations and planned follow-up care in adults with common musculoskeletal conditions. The main questions it aims to answer are:

  • Does reading a brief reassurance message before a clinic visit change how interested patients are in additional care, such as follow-up visits, tests, injections, or surgery?
  • Does the message affect whether patients actually schedule follow-up care after the visit?

Researchers will compare participants who receive the pre-visit reassurance message to those who receive usual care to see if the message changes patients' enthusiasm for care or their follow-up decisions.

Participants will:

  1. Read a short, easy-to-understand message about musculoskeletal symptoms and options for care (for those in the intervention group)
  2. Complete a brief questionnaire rating their interest in follow-up visits, tests, injections, or surgery
  3. Have their scheduled follow-up care recorded after the clinic visit

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Care Provider)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adult (18+ years)
  • English or Spanish language literacy
  • Seeking musculoskeletal specialty care
  • Diagnosed with any non-traumatic musculoskeletal condition
  • New or return patient to clinic

Exclusion Criteria

  • Cognitive or other impairment precluding completion of a survey on a tablet
  • Acute traumatic pathophysiology (fracture, dislocation, sprain/strain)

Arms & Interventions

Intervention Arm (Nudge / Reassurance Message)

Experimental

Participants randomized to the intervention group will read a brief, easy-to-understand message (generated by a Large Language Model) before their musculoskeletal clinic visit. The message explains that many musculoskeletal symptoms are common, often related to normal body changes, and can improve with simple self-care. It emphasizes that visits, tests, injections, and treatments are often optional, and patients can decide how much care they wish to pursue. After reading the message, participants will complete a short questionnaire rating their interest in follow-up visits, tests, injections, and surgery. Clinicians providing care will be blinded to participants' group assignment.

Intervention: Nudge intervention (Behavioral)

Control arm (Usual Care)

No Intervention

Participants randomized to the control group will receive usual care prior to their musculoskeletal clinic visit, without any pre-visit reassurance message. They will complete the same questionnaire rating their interest in follow-up visits, tests, injections, and surgery. Clinicians providing care will be blinded to participants' group assignment.

Outcomes

Primary Outcomes

Pre-visit enthusiasm for additional care

Time Frame: Immediately after intervention

The primary outcome is pre-visit enthusiasm for additional care, measured as participants' self-reported interest in pursuing a return visit, diagnostic tests, physical therapy, injections, or surgery. Participants rate each item on a 0-10 scale, where 0 indicates "not at all interested" and 10 indicates "definitely want it." This outcome is assessed immediately after the intervention (or usual care) and before the clinic visit.

Secondary Outcomes

  • Actual scheduled follow-up care(Immediately following clinic visit)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

David Ring

Associate Dean for Comprehensive Care; Professor and Associate Chair for Faculty Academic Affairs, Department of Surgery and Perioperative Care; Courtesy Professor of Psychiatry and Behavioral Sciences

University of Texas at Austin

Study Sites (1)

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