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Contraception Decision Aid Use and Patient Outcomes

NCT05177783 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2022-05-02

No results posted yet for this study

Summary

The purpose of this study is to assess the impact of a contraception decision aid mobile application on: (a) decisional conflict, (b) reproductive health self-efficacy, (c) contraceptive and reproductive health literacy, and (d) contraceptive use intentions.

Conditions

  • Contraceptive Usage

Interventions

BEHAVIORAL

Tuune health questionnaire

Participants complete the Tuune contraceptive decision aid health questionnaire.

BEHAVIORAL

Control health questionnaire

Participants complete a standard physician intake health questionnaire.

Sponsors & Collaborators

  • Texas Christian University

    lead OTHER

Principal Investigators

  • Sarah Hill, PhD · Texas Christian University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
34 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-15
Primary Completion
2022-05-30
Completion
2022-08-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05177783 on ClinicalTrials.gov