- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04213625
Do Patients Perceive Surgeons Who Provide Personal Information as More Trustworthy and Empathetic?
Do Patients Perceive Surgeons Who Provide Personal Information ("Self-disclosure") as More Trustworthy and Empathetic?
Prior studies have shown that patient trust in their physician is associated with better health outcomes and lower levels of emotional distress. Patients who have low levels of trust in their physician are less satisfied and less likely to adhere to their physician recommendations. As such, there is a need to better understand factors related to patient trust in their physician.
Purpose: To understand whether patient awareness of a surgeon's personal background improves patient trust in their surgeon.
Study Overview
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients (age 18 years or greater) visiting a single orthopaedic hand surgeon
- English fluency and literacy
- Ability to take informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control Group
Information sheet with only their surgeon's educational background.
|
|
Experimental: Intervention
Experimental group will receive an information sheet with their surgeon's educational and personal background.
|
Experimental group will receive an information sheet with their surgeon's educational and personal background. Personal Background
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Wake Forest -Trust in Physician score
Time Frame: Immediately after the clinic visit, patients are given the survey to complete.
|
Before the clinic visit, the research assistant will give patients a sheet that gives them info on their surgeon.
Control group will receive an information sheet with only their surgeon's educational background.
Experimental group will receive an information sheet with their surgeon's educational and personal background.
Immediately after the clinic visit, the research assistant will ask patients to complete Wake Forest Trust in physician survey.
Response choices (coding) are: Strongly Agree (5), Agree (4), Neutral (3), Disagree (2), Strongly Disagree (1).
Responses are summed (range 5-25) with higher scores indicating more trust.
|
Immediately after the clinic visit, patients are given the survey to complete.
|
Jefferson Scale of Perceived Physician Empathy
Time Frame: Immediately after the clinic visit, patients are given the survey to complete.
|
Before the clinic visit, the research assistant will give patients a sheet that gives them info on their surgeon.
Control group will receive an information sheet with only their surgeon's educational background.
Experimental group will receive an information sheet with their surgeon's educational and personal background.
Immediately after the clinic visit, the research assistant will ask patients to complete the Jefferson Scale of Patient Perceptions of Physician Empathy.
Each item is answered on a 7-point Likert-type scale (from Strongly Disagree = 1 to Strongly Agree = 7), with higher score indicating more empathy.
|
Immediately after the clinic visit, patients are given the survey to complete.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- 2019-06-0047
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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