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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05177783
Study type Interventional
Source Texas Christian University
Contact Sarah E Hill, PhD
Phone 8172576424
Email s.e.hill@tcu.edu
Status Recruiting
Phase N/A
Start date January 15, 2022
Completion date August 30, 2022

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