Wilson 2014.

Methods	Design: RCT Location: Philadelphia, PA (USA) Time frame: March to September 2013 Sample size estimation and outcome of focus: no information
Participants	General with N: 110 women Inclusion criteria: women 13 to 21 years old desiring contraception; not taking contraception or not satisfied with current method; and not desiring pregnancy in next 12 months Exclusion criteria: pregnant or desiring pregnancy in next 12 months
Interventions	Intervention: routine care plus brief peer counseling where mentor describes positive experience with LARC and participant asks questions related to mentor's experience; duration < 10 minutes Comparison: routine care
Outcomes	Primary: chose LARC after contraceptive counseling (IUD or implant inserted after counseling) Secondary: maintained LARC uptake; positive opinion of LARC as primary choice of birth control Follow‐up: 4 months
Notes	Information from conference abstract and ClinicalTrials.gov listing Abstract has results from initial visit only; 4‐month assessment planned 16 July 2015: Wrote to investigator (C Schreiber) regarding when 4‐month results might be available.

LARC: long‐acting reversible contraception
 RCT: randomized controlled trial