Assessing Satisfaction With Contraceptive Counseling Using Telephone Versus Video Telehealth Visits

Contraception Clinical Trial

Official title:

Pilot Randomized Controlled Trial to Assess Satisfaction With Contraceptive Counseling Using Telephone Versus Video Telehealth Visits

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05317468
• Other study ID #: 202203067
• Status: Recruiting
• Phase: N/A
• Start date: June 1, 2022
• Est. completion date: August 31, 2023

Study information

• Verified date: June 2022
• Source: Washington University School of Medicine
• Contact: Rachel Paul, MPH
• Phone: (314) 747-8176
• Email: paulr[@]wustl.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: August 31, 2023
• Est. primary completion date: April 30, 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 14 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Contraception
• Health Care Utilization

Intervention

Other:
• Contraceptive Counseling
Patients will receive contraceptive counseling to review all available contraceptive methods prior to their visit with a clinician.

Locations

Country	Name	City	State
United States	Washington University School fo Medicine	Saint Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Washington University School of Medicine	Society of Family Planning

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient Satisfaction Assessed by IQFP	Interpersonal Quality in Family Planning (IQFP) scale; Continuous score: 11-55, higher scores indicate higher patient satisfaction Dichotomous: highest score (55) versus lower scores, highest score indicates highest patient satisfaction	Baseline
Secondary	% of Patients Receiving Desired Contraceptive Method Assessed by Medical Record Review		30 Days Post Baseline
Secondary	% of Patients Reporting Barriers to Technology Use Assessed by Baseline Questionnaire	Percentage of patients reporting limited access to mobile telephone or computer with video capabilities, unreliable telephone or internet service, and environmental distractors (i.e. loud noises, lack of privacy)	Baseline