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Contraception Decision Aid Use and Patient Outcomes

T

Texas Christian University

Status

Unknown

Conditions

Contraceptive Usage

Treatments

Behavioral: Tuune health questionnaire
Behavioral: Control health questionnaire

Study type

Interventional

Funder types

Other

Identifiers

NCT05177783
TCU020519781

Details and patient eligibility

About

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.

Full 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.

Enrollment

500 estimated patients

Sex

Female

Ages

18 to 34 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Triple Blind

500 participants in 2 patient groups

Tuune
Experimental group
Description:
Participants complete the Tuune contraceptive decision aid health questionnaire.
Treatment:
Behavioral: Tuune health questionnaire
Control
Active Comparator group
Description:
Participants complete a standard physician intake health questionnaire.
Treatment:
Behavioral: Control health questionnaire

Trial contacts and locations

1

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Central trial contact

Sarah E Hill, PhD; Summer Mengelkoch, MS

Data sourced from clinicaltrials.gov

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