Female Patient Preferences Regarding Physician Gender

October 19, 2022 updated by: TriHealth Inc.

Female Patient Preferences Regarding Physician Gender; is There a Difference? A National Survey

This is a cross sectional survey study to describe female patient preferences when choosing their OB/GYN and other providers.

Study Overview

Status

Completed

Detailed Description

The American College of Obstetricians and Gynecologists (ACOG) published that as of 2009, 79.7% of the Obstetrics and Gynecology residents were female. Given the striking decline in male providers selecting OB/GYN in more recent years, it is critical to characterize patient preferences in the current environment.

Nevertheless, it is not clear that females have strong preferences regarding gender. We hope to better understand the influence of bias on physician gender in present day.

The purpose of this study is to describe female population preference based on physician gender and specialty.

The study will be conducted on an online platform distributed across the United States by the aid of SurveyMonkey® .

Study Type

Observational

Enrollment (Actual)

1015

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ohio
      • Cincinnati, Ohio, United States, 45220
        • Cincinnati Urogynecology Associates

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Female population residing in the USA

Description

Exclusion Criteria:

  • Unwillingness to participate in the study
  • Lack of access to the internet
  • Non-English speaking

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of Female Respondents Having Their Preferences Based on Physician Gender for the OB/GYN Care
Time Frame: During a 10 minute period of completing the survey electronically
Proportion of female respondents whose responses are "Male physician" or "Female physician" over "No preference" for the question 15, "For my obstetrician/gynecologist, overall I would prefer a..."
During a 10 minute period of completing the survey electronically
Proportion of Female Respondents Having Their Preferences Based on Physician Gender for the Primary Care Physician
Time Frame: During a 10 minute period of completing the survey electronically
Proportion of female respondents whose responses are "Male physician" or "Female physician" over "No preference" for the question 16, "For my primary care physician, overall I would prefer a..."
During a 10 minute period of completing the survey electronically

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Rachel Pauls, MD, TriHealth - Cincinnati Urogynecology Associates

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 5, 2019

Primary Completion (Actual)

March 6, 2019

Study Completion (Actual)

May 6, 2019

Study Registration Dates

First Submitted

January 10, 2019

First Submitted That Met QC Criteria

January 18, 2019

First Posted (Actual)

January 22, 2019

Study Record Updates

Last Update Posted (Actual)

September 1, 2023

Last Update Submitted That Met QC Criteria

October 19, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 18-113

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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