- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03403660
Physician Attire and Appreciation of Physician Communication in Postpartum Women
Wearing white coat during hospital rounds has been associated with increased risk of colonization and transmission of resistant pathogens. On the other hand, studies have shown that physicians' attire affects patients' confidence in their physician and the patient-physician relationship. The results of these studies were highly dependent on the practice setting, with no data in postpartum patients.
The objective is to test the hypothesis that not wearing a white coat during physician postpartum rounds impact patient-physician communication scores.
Study Overview
Detailed Description
Patient satisfaction is an important measure of quality of care. One of the most important variables in patients satisfaction scores is the physician communication skills. There have been several studies evaluating different strategies to improve the patient perceptions of patient - physician communication including delayed physician rounds, improvement of handoff strategies, and family centered rounds. Additionally, research has shown that patients develop a first impression of their physician based on the physician's verbal and nonverbal communication, including the clothing and cleanliness. Patient - physician communication scores not only have an impact on patient care, but are also now linked to Medicare reimbursements.
White coats have been widely used in the medical profession, however some physicians believe that this can be a nonverbal barrier to patient's interaction. Prior studies on the impact of physician attire have reported conflicting results. In a survey published by Cha et al, obstetric and gynecologic patients seen in the outpatient clinic preferred that the resident use white coats. Another study showed that patients favor the use of white coat in the Internal Medicine outpatient clinic which may favorably influence trust and confidence in the medical encounter.
No randomized controlled trial has been published on the impact of the use of white coat on patient - physician communication scores in the postpartum patients. This trial's primary outcome is to evaluate the impact of physician attire (specifically wearing white coat) during postpartum rounds on "patient - physician communication" scores.
This study is a randomized controlled trial performed in postpartum patients to evaluate the impact of not wearing white coat during rounds on "patient - physician communication" scores.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Texas
-
Galveston, Texas, United States, 77550
- Universty of Texas Medical Branch
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Maternal age ≥ 18 years and <50 years
- Patient admitted to postpartum floor at University of Texas Medical Branch (UTMB)
- Patient care managed by obstetric physicians during the postpartum period.
Exclusion Criteria:
- Patient admitted to ICU
- Delivery resulting in stillbirth Patient not fluent in Spanish and/or English
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: non white coat rounding
The postpartum physician rounding in this group will be performed wearing white coat.
|
Postpartum patients are randomized to either arm of the study (white coat or standard scrub suit only) by location.
All the obstetric physicians associated with patient's postpartum care should use or not use white coat in every single encounter with patient.
|
Placebo Comparator: White coat rounding
The postpartum physician rounding in this group will be performed not wearing white coat.
|
Postpartum patients are randomized to either arm of the study (white coat or standard scrub suit only) by location.
All the obstetric physicians associated with patient's postpartum care should use or not use white coat in every single encounter with patient.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient - physician communication score
Time Frame: 24 to 120 hours
|
Obtained from the three Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) questions.
|
24 to 120 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hospital rating scores
Time Frame: 24 to 120 hours
|
Obtained from one question of the HCAHPS survey
|
24 to 120 hours
|
Recommending the hospital to friends and family
Time Frame: 24 to 120 hours
|
Obtained from one question of the HCAHPS survey
|
24 to 120 hours
|
Physician attire rating score
Time Frame: 24 to 120 hours
|
Rated from 1 to 4
|
24 to 120 hours
|
White coat use
Time Frame: 24 to 120 hours
|
Patient answer if she remember or not if their physician were using white coat.
|
24 to 120 hours
|
Collaborators and Investigators
Investigators
- Study Director: Mauricio La Rosa, MD, University of Texas
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- IRB 17-0096
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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