NCT07104305

Brief Summary

This study aims to test in what way a care strategy incorporating frequent contact can benefit patients with musculoskeletal condition that necessitates some adaptation and resiliency to symptoms and limitations that are expected to be either long-lasting or permanent. Patients will be randomized into either group A, where they will receive the standard amount of contact with their clinician, or group B, in which they will have contact with their clinican more frequently. The communication strategy may utilize text, email, portal, phone, video or other options as agreed on. The frequency will be at least once a week. All patients will complete a set of questionnaires at the end of the visit.

Trial Health

30
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 23, 2019

Completed
5.6 years until next milestone

First Posted

Study publicly available on registry

August 5, 2025

Completed
5 months until next milestone

Study Start

First participant enrolled

January 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

June 10, 2026

Status Verified

June 1, 2026

Enrollment Period

2 months

First QC Date

December 23, 2019

Last Update Submit

June 6, 2026

Conditions

Keywords

MusculoskeletalOrthopedicsMental healthPatient-Clinician relationship

Outcome Measures

Primary Outcomes (1)

  • Guttman Satisfaction scale

    The Guttman Satisfaction Scale is a unidimensional questionnaire designed to measure the degree of patient satisfaction with the care they received. It consists of a series of hierarchically ordered yes/no items, with each successive item indicating a higher level of satisfaction. Total scores range from 0 to 7, with higher scores reflecting greater satisfaction, representing a better outcome.

    1 month after enrollment

Secondary Outcomes (5)

  • PROMIS Physical Function CAT

    1 month after enrollment

  • Negative Pain Thoughts Questionnaire (NPTQ-4)

    1 month after enrollment

  • PROMIS Depression CAT

    1 month after enrollment

  • Jefferson Scale of Patient's Perceptions of Physician Empathy (JSPPE)

    1 month after enrollment

  • Communication effectiveness

    1 month after enrollment

Study Arms (2)

Standard care

NO INTERVENTION

Patients in this arm will receive the standard amount of contact with their clinician.

High-contact communication strategy

EXPERIMENTAL

Patients will have contact with their clinician more frequently. The communication strategy may utilize text, email, portal, phone, video or other options as agreed on. The frequency will be at least once a week. All patients will complete a set of questionnaires at the end of the visit.

Behavioral: High-contact communication strategy

Interventions

Patients will have contact with their clinician more frequently. The communication strategy may utilize text, email, portal, phone, video or other options as agreed on. The frequency will be at least once a week. All patients will complete a set of questionnaires at the end of the visit.

High-contact communication strategy

Eligibility Criteria

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

You may qualify if:

  • Adult patient
  • New or return visit
  • English or Spanish speaker
  • A musculoskeletal condition that necessitates some adaptation and resiliency to symptoms and limitations that are expected to be either long-lasting or permanent

You may not qualify if:

  • Cognitive dysfunction
  • Language other than English or Spanish

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Texas Health Austin (UTHA)

Austin, Texas, 78701, United States

Location

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: New or return patients with some opportunity to better adapt to a long-standing or permanent symptoms will be randomized to a high-contact communication strategy agreed on by the clinician and patient or standard care (the patient initiates between visit contact as needed). The communication strategy may utilize text, email, portal, phone, video or other options as agreed on. The frequency will be at least once a week. All patients will complete a set of questionnaires at the end of the visit. At the end of the initial visit and 1 month after enrollment, people will be contacted by their method of choice to repeat the questionnaires.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, Dean associate of surgery department

Study Record Dates

First Submitted

December 23, 2019

First Posted

August 5, 2025

Study Start

January 1, 2026

Primary Completion

March 1, 2026

Study Completion

March 1, 2026

Last Updated

June 10, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations