N/A N=984 Randomized Single-blind Prevention

MyNewOptions: An Online Study of Reproductive Life Planning and Contraceptive Action Planning

Contraceptive Use · Unintended Pregnancy

Bottom Line

View on ClinicalTrials.gov: NCT02100124 ↗

Enrolled (actual)

984

Serious AEs

0.0%

Results posted

Jul 2018

Primary outcome: Primary: Contraceptive Use — 93.43; 94.46; 94.10 percentage of surveys — p=1.0

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Reproductive Life Planning (RLP) (Behavioral); Contraceptive Action Planning (Behavioral); Contraception information (Behavioral)
Age: Adult · 18+ yrs
Sex: Female
Sponsor: Milton S. Hershey Medical Center
Primary completion: Sep 2016

Outcome Measures

Outcome	Result	p-value
PRIMARY Contraceptive Use	93.43; 94.46; 94.10	1.0
SECONDARY Effectiveness of Contraceptive Method	60.66; 63.93; 63.19	0.48
SECONDARY Contraceptive Method Satisfaction	58.22; 57.09; 57.70	1.0
SECONDARY Contraceptive Adherence	74.02; 73.27; 76.37	1.0

Summary

The purpose of this web-based study is to determine whether reproductive life planning (RLP), with or without contraceptive action planning (RLP+), will result in reduced risk of unintended pregnancy when compared to an information-only control group.

Eligibility Criteria

Inclusion Criteria

not currently pregnant
sexually active with a male partner in the past 6 months OR anticipate being sexually active with a male partner in the next 6 months
does not intend pregnancy in the next 12 months
has Internet access and email address

Exclusion Criteria

tubal sterilization
hysterectomy
partner with vasectomy

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02100124). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.