NCT05177783

Contraception Decision Aid Use and Patient Outcomes

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 500 (estimated)
• Sponsor: Texas Christian University · Academic / Other
• Sex: Female
• Age: 18 Years – 34 Years
• Healthy volunteers: Accepted

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.

Detailed description

After being informed about the study and the potential risks, all participants giving written informed consent will be randomly assigned in a double-blind manner (participant and investigator) in a 1:1 ratio to complete an interactive contraception decision aid health questionnaire (Tuune) or a standard medical questionnaire (Control). After, all participants will be asked questions assessing: (a) decisional conflict, (b) reproductive health self-efficacy, (c) contraceptive and reproductive health literacy, and (d) contraceptive use intentions.

Conditions

• Contraceptive Usage

Interventions

Type	Name	Description
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.

Timeline

• Start date: 2022-01-15
• Primary completion: 2022-05-30
• Completion: 2022-08-30
• First posted: 2022-01-05
• Last updated: 2022-05-02

Locations

1 site across 1 country: United States