Beyond Bias - Reducing Provider Bias Towards Adolescents to Increase Contraception Take-Up in Tanzania, Burkina Faso, and Pakistan

Family Planning Services Clinical Trial

Official title:

Beyond Bias - Reducing Provider Bias Towards Adolescents to Increase Contraception Take-Up in Tanzania, Burkina Faso, and Pakistan

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04802304
• Other study ID #: 2019-0387
• Status: Completed
• Phase: N/A
• Start date: September 1, 2020
• Est. completion date: October 14, 2022

Study information

• Verified date: October 2022
• Source: RAND
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Beyond Bias will evaluate the impact of an intervention designed to reduce family planning provider bias towards young, unmarried, and nulliparous women in Tanzania, Burkina Faso, and Pakistan. The intervention has three components: 1) a summit that includes impactful stories told to and by family planning providers that highlight the consequences of provider bias, 2) a forum for continued communication between providers, and 3) a rewards program where clinics in which providers exhibit less biased client interactions or who have improved the most towards this end will be rewarded with social recognition and a ceremony. Half of the eligible clinics in each country (233 in total) are randomly assigned to receive the intervention, while the remaining half serves as control. The objective of the evaluation is to estimate the impact of the intervention on a range of outcomes related to quality of family planning care among young, unmarried, and nulliparous women. The investigators hypothesize that the intervention will increase the share of young, unmarried, and nulliparous women who received counseling on a range of methods, counseling on long acting methods, and who received their preferred method. The investigators will collect four types of data to evaluate the intervention: 1) provider surveys, 2) mystery clients' visits, 3) direct observations of client-provider interactions, and 4) qualitative interviews with clients, providers, and implementors.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 233
• Est. completion date: October 14, 2022
• Est. primary completion date: September 1, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: N/A to 24 Years

Eligibility

Inclusion Criteria for Providers:

• All providers that are part of Pathfinder Internal's supported clinic network in Burkina Faso, Tanzania, and Pakistan.

Exclusion Criteria for Providers:

• None

Inclusion Criteria for Clients:

• All clients aged 24 or under that visit a clinic that is enrolled in the study

Exclusion Criteria for Providers:

• Clients over 24
• Clients who do not visit the clinic for family planning services

Related Conditions & MeSH terms

• Family Planning Services

Intervention

Other:
• Beyond Bias Treatment
The intervention has three components: 1) a summit that includes impactful stories told to and by family planning providers that highlight the consequences of provider bias, 2) a forum for continued communication between providers, and 3) a rewards program where clinics in which providers exhibit less biased client interactions or who have improved the most towards this end will be rewarded with social recognition and a ceremony.

Locations

Country	Name	City	State
United States	RAND	Santa Monica	California

Sponsors (4)

Lead Sponsor	Collaborator
RAND	Bill and Melinda Gates Foundation, Pathfinder International, University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Whether client was able to receive services	This is a measure of whether the client received family planning services on the day they came into the clinic. This will be measured from real clients using client exit surveys and using mystery clients.	12 months after the intervention starts
Primary	Optimal Counseling	This is a measure of whether the client was counseled on all methods that were good options for the client given her background and preferences. This will be coded as 1 if client was counseled on the full set of optimal family planning methods and zero if the client was not counseled on the full set of optimal family planning methods. This will be collected in the client exit survey and in by mystery clients.	12 months after the intervention starts
Primary	Received modern method	This is a measure of whether the client received a modern family planning method during her visit. This will be collected in the client exit survey only.	12 months after the intervention starts
Primary	Perceived patient centeredness	This is a composite scale (ranging from 0 to 1) that measures the extent to which the client perceived the her interaction with family provider as patient centered. The questions included in the scale will be chosen based on data driven factor analysis methods. Higher scores will indicate better patient centeredness. This will be collected in the client exit survey and in by mystery clients.	12 months after the intervention starts
Secondary	Provider biased attitudes	This is a composite scale (ranging from 0 to 1) that measures the extent to which providers have biased attitudes towards young, unmarried, and adolescent women. The questions included in the scale will be chosen based on data driven factor analysis methods. Higher scores will indicate better patient centeredness. This will be collected through a provider survey.	12 months after the intervention starts