Measuring and Displaying the Subjective

Not Applicable

Completed

• Conditions: Physician-Patient Relations; Communication Research

• Registration Number: NCT06490224
• Lead Sponsor: University of Texas at Austin

Brief Summary

The investigators developed a brief set of subjective health measures designed to feel more relevant to patients seeking musculoskeletal specialty care, presented the scores to patients and clinicians using an easy-to-understand visual display, and measured whether or not this process harmed patient experience.

Detailed Description

Musculoskeletal patient-reported outcome measures (PROMs; measures of levels of discomfort and incapability) were originally designed as tools for clinical research as were other self-reported measures of the subjective aspects of illness such as mental health measures. PROMs and mental health measures are increasingly used in clinical practice with individual patients. A few areas for improvement are noted in the use of questionnaires in musculoskeletal specialty care, including relevancy, understandability, and their confusing use in heath strategies. The investigators sought to assess the impact of an enhanced and more personalized self-reported health measurement strategy to address some of these opportunities by developing a brief set of items addressing levels of discomfort, incapability, mental, and social health designed to feel relevant to musculoskeletal specialty care and resulting in an easy-to-understand display that can be a communication tool for patients and clinicians.

Study Timeline

• Study Start: 2023-11-19
• Primary Completion: 2024-02-27
• Study Completion: 2024-04-06
• Status Verified: 2024-06
• Study First Submitted: 2024-06-25
• Study First Submitted QC: 2024-06-28
• Last Update Submitted: 2024-06-28
• Study First Posted: 2024-07-08
• Last Update Posted: 2024-07-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

• All new and return patients
• English and Spanish speakers

Exclusion Criteria

• Cognitive deficiency precluding PROM completion
• Language other than English or Spanish

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Jefferson Scale Patient Perceptions of Physician Empathy (JSPPPE)	Immediately after the intervention	Patient perceived clinician empathy (Numerical scale from 1-35; Higher scores equal better outcome)
CollaboRATE survey	Immediately after the intervention	Quality of shared decision-making (Numerical scale from 1-27; Higher scores equal better outcome)

Trial Locations

Locations (1)

University of Texas at Austin; 🇺🇸 Austin, Texas, United States