- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04315402
The Impact of Provider Demographics on Patients' Continuity of Care
October 9, 2020 updated by: TriHealth Inc.
The race concordance of providers to their patients impacts a patient's investment and agency in the patient-provider relationship.
The mistrust of medicine within the African American population remains and patients feel unengaged in their care.
Race concordant provider-patient rela-tionships would improve the equity of patient care in our clinic.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The patients of the obstetrics and gynecology resident clinic at Good Samaritan Hospital have a poor follow-up rate for their gynecologic and prenatal care visits.
In addition, patients oftentimes voice frustration over the care that they receive and sometimes remark that they feel their provider was "racist."
These patients often have complex social situations that cannot be solved in one office visit but perhaps the providers' ability to gain the trust of the minority patients is inadequate.
The residents in the OB/GYN program are 80% white with no African American representation.
If patients are unable to connect with caregivers due to cross-cultural differences, this could be remedied by training current residents in cross-cultural communication or re-cruitment of a resident class more representative of the majority African American patient population.
This project will provide perspective on the minority patients' needs in the provider-patient relationship and allow providers to reexamine their ability to gain trust with the ultimate goal to increase follow-up rates.
Follow-up rates for prenatal care are directly linked to improved maternal and fetal outcomes.
The investigators goals are threefold: to gain clarity on whether or not a more diverse resident group would be helpful in gaining the trust of patients, to assess the current state of the well-established historical and generational mistrust of medical care by the African American patients of the clinic, and to explore how patient perception of their provider impacts their rate of follow up in the large community hospital clinic.
Study Type
Observational
Enrollment (Anticipated)
415
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
- Recruiting
- TriHealth Good Samaritan Hospital
-
Contact:
- Ganga Devaiah, MS
- Email: ganga_devaiah@trihealth.com
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
- Patients of the Faculty Medical Center seeing OB/GYN residents
- Those requiring follow-up (less than 6 months)
Description
Inclusion criteria
- Female Patient seeing OB/GYN resident at FMC
- 18 years or older
- <36 weeks pregnant or GYN patient
- If GYN patient, must have problem requiring follow-up within 6 months
- Have not previously completed the survey
Exclusion criteria
- Less than 18 years of age
- High risk clinic patients (Tuesday afternoons)
- Patients without a follow-up less than 6 months as scheduled at check out
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Group 1 (provider-patient concordant)
|
|
Group 2 (provider-patient discordant)
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient's rate of follow-up
Time Frame: 6 months
|
Whether or not patient was present at their next scheduled GYN or OB follow-up appointment.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nima Patel, MD, TriHealth Inc.
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)
August 12, 2020
Primary Completion (Anticipated)
March 1, 2021
Study Completion (Anticipated)
March 1, 2021
Study Registration Dates
First Submitted
March 17, 2020
First Submitted That Met QC Criteria
March 17, 2020
First Posted (Actual)
March 19, 2020
Study Record Updates
Last Update Posted (Actual)
October 12, 2020
Last Update Submitted That Met QC Criteria
October 9, 2020
Last Verified
October 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- 19-105
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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