A Randomized-Controlled Trial to Increase the Uptake of LARCs in Cameroon

NCT03733678 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2500

Last updated 2025-05-14

No results posted yet for this study

Summary

Cameroon exhibits a high and non-decreasing level of maternal mortality (roughly 600 per 100,000 live births), partially related to its relatively high total fertility rate (roughly 4.6). Survey evidence furthermore suggests that a significant fraction of these pregnancies is unwanted or considered mistimed by the mother, especially among females aged 15-19. Despite this, the rate of utilization of family planning (FP) is low: e.g. only 48% of sexually active unmarried women use any form of (modern) contraception, or MC, and even then, it is primarily condoms. The use of LARCs (long-acting reversible contraceptives, i.e. the IUD and implant) is less than 1% according to the most recent Demographic Health Survey.

The study investigators propose to use an integrated behavioral science approach to increase the take-up of both SARCs (short-acting reversible contraceptives, i.e. the pill and injectable) and especially LARCs among reproductive-age females in Cameroon, including adolescents who may be unmarried and/or nulliparous. In addition to decreasing maternal mortality and undesired pregnancies, indirect effects for the community will include: increased welfare from reduced side effects that arise due to current one-size-fits-all FP counseling; healthier children due to improved birth spacing; and increased human capital formation both for children and for young (often school-aged) potential mothers.

The study investigators propose to conduct the study at HGOPY for a duration of 12 months. The study investigators will provide tablets to each of five nurses that conduct FP counseling to participants at the hospital. The tablets contain a counseling "app" (or decision-support tool or a job-aid) that was jointly developed by professionals from HGOPY, the World Bank, and the Ministry of Health. The study investigators propose an individually-randomized experiment, where the participants will be offered randomly varying discounts for the modern contraceptive methods they wish to adopt. The study investigators also propose to experiment with certain aspects of the "app" to improve its effectiveness - both for the participant and for the nurse. More details on the experimental design are provided below.

Conditions

  • Contraception
  • Contraception Behavior
  • Contraceptive Usage
  • Contraceptive Method Switching

Interventions

BEHAVIORAL

Price discounts for SARCs

SARCs are offered free to the client

BEHAVIORAL

Price discounts for LARCs

LARCs are offered at lower prices to the client

BEHAVIORAL

Sequential vs. simultaneous recommendations

Top ranked methods are presented to the client sequentially or simultaneously

Sponsors & Collaborators

  • Stanford University

    collaborator OTHER
  • George Washington University

    collaborator OTHER
  • University of Exeter

    collaborator OTHER
  • University of California, San Diego

    collaborator OTHER
  • Yaounde Gynecology, Obstetrics and Pediatrics Hospital

    collaborator UNKNOWN
  • World Bank

    lead OTHER

Principal Investigators

  • Berk Ozler, PhD · World Bank

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
SEQUENTIAL

Eligibility

Min Age
10 Years
Max Age
49 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-03-23
Primary Completion
2022-12-31
Completion
2024-12-31

Countries

  • Cameroon

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03733678 on ClinicalTrials.gov