- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04932993
Writing Down Goals
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
People's stated preferences are often inconsistent with what matters most to them (their values). And they are often based on misconceptions, distress, and less effective cognitive coping strategies. For instance, a person might say "My goal is to have no pain" when that is not possible. Or they might say "My goal is to get the shot that fixes this" when there is no such shot. It may go without saying that people want: "To be able to live a normal lifestyle" and "To be able to accomplish most of their goals." In other words, people want to be able to be themselves. They are seeking care because they are not able to be themselves or they are concerned that they may not be able to be themselves. The word health comes from an old German word meaning "whole."
One part of good health is correcting or alleviating pathophysiology (e.g. reading glasses). Another part of good health is evolving one's inner narrative (e.g. "I'm older now and need glasses to read").
The women's health IPU at UT Health Austin is happy with having patients write down their goals at their first visit and then tracking those. It would be interesting to study people seeking musculoskeletal specialty care to determine whether asking patients what result of their care would be rated a success helps direct the clinician-patient interaction in a more fruitful direction compared to the usual clinical interaction.
Study Type
Phase
- Not Applicable
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adult patients (18+)
- Orthopedic visit
Exclusion Criteria:
- Patients who are illiterate.
- Patients who do not speak English.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Standard care
Will not write down goals their goals for their medical care (usual care).
|
|
|
Experimental: Writing down goals
Will write down goals their goals for their medical care.
|
Patient will write their health goals down before the visit.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Decision conflict questionnaire
Time Frame: Baseline
|
Questionnaire assessing decision conflict
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Decision regret questionnaire
Time Frame: Baseline
|
Questionnaire assessing the degree of regret of decision
|
Baseline
|
|
Jefferson Scale of Patient's Perceptions of Physician Empathy
Time Frame: Baseline
|
Patient perceived of physician empathy as measured by the JSPPE
|
Baseline
|
|
Patient Activation Measure-13
Time Frame: Baseline
|
Patient activation as measured by PAM-13
|
Baseline
|
|
Guttman Satisfaction scale
Time Frame: Baseline
|
Questionnaire measuring to what degree patients are satisfied with the care they received.
|
Baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: David Ring, MD, PhD, Professor of Surgery, Dell Medical School at The University of Texas at Austin
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019-07-0089
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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