miPlan: A Trial of miPlan Intervention vs. Standard of Care

Completed · Not applicable

Conditions studied: Unintended Pregnancy

In brief

Using our experience in digital media, behavior theory, client-centered interventions, and family planning, we have prototyped a digital application ("app")-miPlan-to be used in the clinic waiting room prior to a contraceptive visit. The goal of this research is to refine the app and conduct a randomized controlled trial of the miPlan intervention vs. standard care. The aim of this study is to understand miPlan's impact. The primary outcome is LARC uptake at clinic discharge. The secondary outcomes are contraceptive use at discharge, self-efficacy and decisional balance for highly effective contraception post-app use, contraceptive satisfaction, and intention to continue method use. The research will consist of baseline activities as well as a three-month follow-up call.

Key facts

Study ID

NCT02396602

Run by

University of Chicago

People needed

225

Starts

2015-02-01

Expected to finish

2016-08-01

Last updated by the study team

2016-08-25

Who can join

Age: 15 and older, up to 29. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• African American or Latina female and sexually active with a male partner(s) within the past 6 months,
• age 15 to 29 years
• present for contraception initiation
• English speaking

You may not qualify if…

• not currently pregnant or intending pregnancy within the next 6 months
• and not currently using LARC
• not highly intending LARC at enrollment

Where it is running

• Planned Parenthood Illinois, Englewood Health Center — Chicago, Illinois, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.