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.
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 contraceptive counseling. The aim of this study is to understand miPlan's impact in terms of contraceptive knowledge, intentions and behaviors. The primary outcome is LARC uptake, which will be measured via chart review at clinic discharge, i.e. immediately following a patient's family planning visit. The secondary outcomes are contraceptive use at discharge (measured via chart review immediately following patient's family planning visit), self-efficacy and decisional balance (both measured via adapted validated scales for each) for highly effective contraception post-app use (measured immediately following intervention and prior to contraceptive counseling session), contraceptive satisfaction (measured at 3 months post baseline), and intention to continue method use (measured at 3 months post baseline). The research will consist of baseline activities as well as a three-month follow-up call.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
225
miPlan mobile contraceptive counseling waiting room app intervention
Planned Parenthood Illinois, Englewood Health Center
Chicago, Illinois, United States
LARC uptake
uptake of the implant or IUD at time of intervention (measured via contraceptive method choice and delivery by checkbox)
Time frame: at time of intervention (baseline (0 weeks)
contraceptive use
use of contraceptive methods at time of intervention (measured via contraceptive method choice and delivery by checkbox)
Time frame: at time of intervention (baseline (0 weeks))
change in self-efficacy for contraception at 12 weeks
change in self efficacy for contraceptive method use (measured via validated 5-item attitudinal scale by Galavotti et al 1995) from baseline to 12 weeks
Time frame: baseline (0 weeks) and 12 weeks
change in decisional balance for highly effective methods at 12 weeks
change in decisional balance for highly effective methods (measured via validated 10-item attitudinal scale by Galavotti et al 1995) from baseline to 12 weeks
Time frame: baseline (0 weeks) and 12 weeks
contraceptive satisfaction
satisfaction with contraceptive method choice (measured by 4-point Likert scale)
Time frame: 12 weeks post-enrollment
intention to continue method use
intention to continue contraceptive method use (measured dichotomously)
Time frame: 12 weeks post enrollment
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