The primary purpose of this research is to conduct a small matched cluster control trial of an intervention designed to address reproductive coercion and unintended pregnancy (ARCHES - Addressing Reproductive Coercion within Healthcare Settings) adapted to the Kenyan cultural and family planning healthcare context (ARCHES Kenya) so as to provide initial data regarding acceptability, feasibility and efficacy in this high-need LMIC context.
Age range
15 Years – 49 Years
Sex
FEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of Participants Reporting Reproductive Coercion
Timeframe: Change from baseline number reporting reproductive coercion at 3 and 6 month follow-up (combined)
Number of Participants Reporting Intimate Partner Violence
Timeframe: Change from baseline number reporting physical intimate partner violence at 3 and 6 month follow-up (combined)
Number of Participants Reporting Sexual Intimate Partner Violence
Timeframe: Change from baseline number reporting sexual intimate partner violence at 3 and 6 month follow-up (combined)
Number of Participants Reporting Uptake of a Modern Contraceptive Method
Timeframe: Assessed at exit interview on month 0 (immediately after baseline and provider appointment)