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Completed

NCT Number: NCT03733678

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

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.

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Key information

Age range

10 year–49 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital gynéco-obstétrique et pédiatrique de Yaoundé (HGOPY)

Yaoundé, Cameroon

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female
  • Ages 10-49
  • Presenting at HGOPY seeking FP counseling/services
  • HGOPY clients referred to the family planning unit for consultation

Exclusion criteria

  • No exclusion criteria

Treatment and study plan

Price discounts for SARCs

Behavioral

SARCs are offered free to the client

Price discounts for LARCs

Behavioral

LARCs are offered at lower prices to the client

Sequential vs. simultaneous recommendations

Behavioral

Top ranked methods are presented to the client sequentially or simultaneously

Primary outcomes

  1. The client adopted a LARC

    Time frame: 1-day

    using data from the counseling sessions

  2. The client adopted a modern contraceptive method (LARC or SARC)

    Time frame: 1-day

    using data from the counseling sessions

Secondary outcomes

  1. Was the client treated with respect by the provider during the counseling session?

    Time frame: 2-weeks

    Self-reported indicator variable using follow-up surveys two weeks after counseling session

  2. Did the client trust the provider during the counseling session?

    Time frame: 2-weeks

    Self-reported indicator variable using follow-up surveys two weeks after counseling session

  3. Did the health provider give information about contraceptive methods that was easy to understand during the counseling session?

    Time frame: 2-weeks

    Self-reported indicator variable using follow-up surveys two weeks after counseling session

  4. Client satisfaction with adopted contraceptive method

    Time frame: 2-week and 16-week measurements

    using 2-week and 16-week follow-up surveys

  5. Discontinuation of adopted contraceptive method

    Time frame: 2-week, 16-week, and 52-week measurements

    using 2-week, 16-week, and 52-week follow-up surveys

  6. Percentage of participants with unintended pregnancy within the time frame

    Time frame: 16-week and 52-week measurements

    using 16-week and 52-week follow-up surveys

Sponsors and collaborators

Lead sponsor

World Bank

Other

Collaborators

  • George Washington University
  • Stanford University
  • University of California, San Diego
  • University of Exeter
  • Yaounde Gynecology, Obstetrics and Pediatrics Hospital

Registry information

Official study title

A Sequential and Adaptive Experiment to Increase the Uptake of Long-acting Reversible Contraceptives in Cameroon

Acronym: HGOPY

Important dates

Study start
2021
Primary completion
2022
Study completion
2024
First posted
Nov 7, 2018
Registry last updated
May 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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