Assessing Satisfaction With Contraceptive Counseling Using Telephone Versus Video Telehealth Visits

NCT ID: NCT05317468

Last Updated: 2024-11-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

214 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-06-01

Study Completion Date

2023-06-26

Brief Summary

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The Contraceptive Choice Center (C3) will compare the patient experience between patients receiving contraceptive counseling using a telephone versus video telehealth model.

Detailed Description

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The Contraceptive Choice Center (C3) will offer contraceptive counseling to patients via telehealth. Participants will be randomized to receive counseling via video or telephone. We will compare patient satisfaction with contraceptive counseling, receipt of desired contraceptive method, and identification of barriers with technology use.

Conditions

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Contraception Health Care Utilization

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Video

Patients will complete contraceptive counseling using a video-based platform. Patients and counselors will have an audio and video connection.

Group Type EXPERIMENTAL

Contraceptive Counseling

Intervention Type OTHER

Patients will receive contraceptive counseling to review all available contraceptive methods prior to their visit with a clinician.

Telephone

Patients will complete contraceptive counseling on a telephone call. Patients and counselors will have an audio connection only.

Group Type EXPERIMENTAL

Contraceptive Counseling

Intervention Type OTHER

Patients will receive contraceptive counseling to review all available contraceptive methods prior to their visit with a clinician.

Interventions

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Contraceptive Counseling

Patients will receive contraceptive counseling to review all available contraceptive methods prior to their visit with a clinician.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Able to speak and read English
* Access to video-capable technology

Exclusion Criteria

* Incarceration
* Unable to provide informed consent secondary to language barrier or cognitive limitation
Minimum Eligible Age

14 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Society of Family Planning

OTHER

Sponsor Role collaborator

Washington University School of Medicine

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jennifer A Reeves, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

Washington University School of Medicine

Locations

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Washington University School of Medicine

St Louis, Missouri, United States

Site Status

Countries

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United States

Other Identifiers

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202203067

Identifier Type: -

Identifier Source: org_study_id

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