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

Sex

ALL

See this in plain English?

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

Questions worth asking your doctor

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.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

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.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

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

Plain-language summary

Who can participate

Sex

ALL

See this in plain English?

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