NCT06078137

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

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

September 28, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

October 11, 2023

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2025

Completed
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

July 31, 2025

Status Verified

July 1, 2025

Enrollment Period

1.3 years

First QC Date

September 28, 2023

Last Update Submit

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

EXPERIMENTAL

Patients 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.

Other: Usual PROMs and new PROMs strategy

Control group

NO INTERVENTION

Patients 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

Intervention Group

Eligibility Criteria

Age18 Years - 89 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

Study Officials

  • David Ring, MD

    Professor of orthopedic surgery at The university of Texas at Austin

    PRINCIPAL INVESTIGATOR

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

Locations