Gilliam 2016.
Methods | Design: individually randomized Location: Chicago, IL (USA) Time frame: February 201 to June 2016 Sample size calculation: no information |
Participants | 22 women Inclusion criteria: African American or Latina; sexually active with male partner in past 6 months; age 15 to 29 years; seeking contraception; English speaking Exclusion criteria: currently pregnant or intending pregnancy in next 6 months; currently using LARC; highly intend to use LARC |
Interventions | Study focus: contraceptive counseling Theory: not specified
|
Outcomes | LARC uptake (at initial visit); method satisfaction at 12 weeks; method continuation at 12 weeks |
Notes | Insufficient information from conference abstract and ClinicalTrials.gov for determining eligibility for review; will consider for inclusion when full report is available |