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Beyond Bias Treatment for Family Planning Services
N/A
Waitlist Available
Led By Zachary Wagner, Ph.D
Research Sponsored by RAND
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
All providers that are part of Pathfinder Internal's supported clinic network in Burkina Faso, Tanzania, and Pakistan.
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months after the intervention starts
Awards & highlights
Study Summary
This trial will evaluate the impact of an intervention designed to reduce family planning provider bias against young, unmarried, and nulliparous women in Tanzania, Burkina Faso, and Pakistan.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months after the intervention starts
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months after the intervention starts
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Optimal Counseling
Perceived patient centeredness
Received modern method
+1 moreSecondary outcome measures
Provider biased attitudes
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: TreatmentExperimental Treatment1 Intervention
Group II: ControlActive Control1 Intervention
Find a Location
Who is running the clinical trial?
RANDLead Sponsor
137 Previous Clinical Trials
510,018 Total Patients Enrolled
University of California, Los AngelesOTHER
1,521 Previous Clinical Trials
10,278,703 Total Patients Enrolled
Bill and Melinda Gates FoundationOTHER
405 Previous Clinical Trials
19,629,991 Total Patients Enrolled
Frequently Asked Questions
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