TerminatedNot Applicable

Developing and Testing Interventions to Address Conscientious Objection to Abortion Care in Mexico and South Africa

Stopped: The study was stopped prematurely due to the COVID-19 pandemic

Mexico, South Africa317 participantsStarted 2020-02-13

Plain-language summary

The primary purpose of this research is to develop strategies and interventions to mitigate the impact of conscientious objection on women's access to safe abortion care in Mexico and South Africa using a user-centered design approach and test the feasibility and effectiveness of these interventions.

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

South Africa Inclusion Criteria: * All staff currently working in selected health facilities * Able to provide informed consent Exclusion Criteria: * Unable to provide informed consent Mexico Inclusion Criteria: * Doctors/anyone eligible to be an abortion provider working in selected health facilities * Able to provide informed consent Exclusion Criteria: * Unable to provide informed consent

What they're measuring

Behavior making it easier for women to access abortion care

Timeframe: Past 30 days

Behavior making it more difficult for women to access abortion care

Timeframe: Past 30 days

Intention to provide abortion service, referral, or information

Timeframe: Next few days

Trial details

NCT IDNCT04290832

SponsorIpas

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-03-17

View on ClinicalTrials.gov More Abortion, Induced trials