Impact of an Enhanced Patient Reported Outcome Measurement (PROM) Strategy on PROM Completion Rates
1 other identifier
interventional
200
1 country
1
Brief Summary
in clinical practice has been curbed by issues related to the variability in use of these tools for decision-making, and universally poor completion rates over time. Patients may not see the relevance of responding to questions about their health, and the results may not be reviewed by the clinician or presented and visualized with the patient. The questions may seem impersonal (e.g. too general and not directly assessing their individual goals, motivations, aspirations), irrelevant (e.g., asking about symptoms of depression when a person is seeking musculoskeletal specialty care) and insensitive (e.g., asking about sensitive subjects at the outset thereby disengaging the individual), and redundant or awkward (e.g., presenting questions that seem very similar or administered in strange orders). Finally, PROMs may also confer some burden (e.g., long PROM questionnaires often used for research may be unnecessarily burdensome for patient care), and provide logistical challenges (e.g., difficulties in administering the tools at the right time points), adding to a poor patient experience.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2023
CompletedFirst Submitted
Initial submission to the registry
September 28, 2023
CompletedFirst Posted
Study publicly available on registry
October 11, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedJuly 31, 2025
July 1, 2025
1.3 years
September 28, 2023
July 28, 2025
Conditions
Outcome Measures
Primary Outcomes (4)
Completion of 3-survey patient-reported outcome measure at 6-week follow-up via Text
We will assess the completion of 3-survey patient-reported outcome measure at 6-week follow-up via Text.
through study completion, an average of 6 weeks
Completion of answered text
We will assess the completion response rate.
through study completion, an average of 6 weeks
Completion of deprioritization options 1 or 2 at 6-week follow-up via text or email
"1 = I got what I needed" "2 = I didn't receive anything useful" "3 = I'm still receiving care"
through study completion, an average of 6 weeks
Jefferson Scale of Patient's Perceptions of Physician Empathy
The Jefferson Scale of Patient's Perceptions of Physician Empathy includes five 7-point scale questions and higher scores indicated greater perceived clinician empathy.
through study completion, an average of 6 weeks
Study Arms (2)
Intervention Group
EXPERIMENTALPatients randomized to intervention receive both usual Patient reported outcome measure (PROM) and new PROMs strategy (on the technology platform for English speakers and on REDCap/Qualtrix for Spanish Speakers) done after rooming.
Control group
NO INTERVENTIONPatients go through the registration process which includes PROMs completion using Ipads. Enrolled in the room at the end of the visit.
Interventions
Patients randomized to intervention receive both usual PROMs and new PROMs strategy
Eligibility Criteria
You may qualify if:
- All new patients English and Spanish speakers
You may not qualify if:
- Cognitive deficiency precluding PROM completion Language other than English or Spanish
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Texas Health Austin
Austin, Texas, 78701, United States
Study Officials
- PRINCIPAL INVESTIGATOR
David Ring, MD
Professor of orthopedic surgery at The university of Texas at Austin
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Surgery and Perioperative Care Department
Study Record Dates
First Submitted
September 28, 2023
First Posted
October 11, 2023
Study Start
September 1, 2023
Primary Completion
January 1, 2025
Study Completion
December 1, 2025
Last Updated
July 31, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share