Child Protective Outcomes Among Ultra-poor Families in Burkina Faso (NCT02415933) | Clinical Trial Compass
CompletedNot Applicable
Child Protective Outcomes Among Ultra-poor Families in Burkina Faso
Burkina Faso720 participantsStarted 2014-10
Plain-language summary
This study tests the effects of family-based economic empowerment intervention, alone and in combination with child rights sensitization component, on child protective outcomes among ultra-poor families in Nord Region, Burkina Faso.
Who can participate
Age range
10 Years – 15 Years
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.
Inclusion criteria
. Household meets locally defined poverty criteria (classified as an ultrapoor household);
. Mother or female caregiver of at least one child between the ages of 10 and 15.
. Child is between the ages of 10 and 15.
. Male head of household provides permission for his wife and child to participate in the study;
. Eligible child and female caregiver/parent can commit to study participation.
Exclusion criteria
. Household doesn't meet locally defined poverty criteria (classified as an ultrapoor household);
. Mother or female caregiver doesn't have at least one child between the ages of 10 and 15.
. Child is not between the ages of 10 and 15.
. Male head of household does not provide permission for his wife and child to participate in the study;
. Eligible child or mother/female caregiver cannot commit to study participation.
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.