Contraception Decision Aid Use and Patient Outcomes

  • STATUS
    Recruiting
  • days left to enroll
    22
  • participants needed
    500
  • sponsor
    Texas Christian University
Updated on 12 May 2022
Accepts healthy volunteers

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.

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.

Details
Condition Contraceptive Usage
Treatment Tuune health questionnaire, Control health questionnaire
Clinical Study IdentifierNCT05177783
SponsorTexas Christian University
Last Modified on12 May 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Females 18 to 34 years of age who enroll to participate in the study, which will take place on the campus of Texas Christian University

Exclusion Criteria

Women who are currently pregnant or breastfeeding
Women who wish to become pregnant within the next 12 months
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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