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CompletedNCT03733678HGOPYUpdated May 14, 2025

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

An interventional study of Price discounts for SARCs and Price discounts for LARCs in Contraception, Contraception Behavior and Contraceptive Usage, sponsored by World Bank. Completed at 1 site in Cameroon. Open to female participants aged 10 Years to 49 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-05-14.

Sponsored by World Bank · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
2,500
Allocation
Randomized
Ages
10 Years to 49 Years
Sex
Female
01

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.

02

Conditions studied

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

Keywords

  • adolescent sexual and reproductive health, maternal mortality, teen pregnancy, LARCs, family planning counseling
03

In context

Contraception Behavior

132 studies on the registry are indexed under Contraception Behavior; 20 are open to participants now.

This study's enrollment of 2,500 is above the median of 382 across 106 interventional studies indexed under Contraception Behavior.

Browse Contraception Behavior studies →

Lead sponsor

World Bank is the lead sponsor of 11 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 49 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

* No exclusion criteria

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Single (Participant)
Enrollment
2,500 participants (actual)

Study arms

  • Experimental
    Free SARC, Free LARC, Recommendation

    Free SARC, Free LARC, Sequential recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs

  • Experimental
    Free SARC, LARC=500, Recommendation

    Free SARC, LARC=500 CFA, Sequential recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs

  • Experimental
    Free SARC, LARC=1000, Recommendation

    Free SARC, LARC=1000 CFA, Sequential recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs

  • Experimental
    Free SARC, LARC=2140, Recommendation

    Free SARC, LARC=2140 CFA, Sequential recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs

  • Experimental
    Free SARC, LARC=5000, Recommendation

    Free SARC, LARC=5000 CFA, Sequential recommendation

    Behavioral: Price discounts for SARCs

  • Experimental
    Regular SARC, Free LARC, Recommendation

    Regular price SARC, Free LARC, Sequential recommendation

    Behavioral: Price discounts for LARCs

  • Experimental
    Regular SARC, LARC=500, Recommendation

    Regular price SARC, LARC=500 CFA, Sequential recommendation

    Behavioral: Price discounts for LARCs

  • Experimental
    Regular SARC, LARC=1000, Recommendation

    Regular price SARC, LARC=1000 CFA, Sequential recommendation

    Behavioral: Price discounts for LARCs

  • Experimental
    Regular SARC, LARC=2140, Recommendation

    Regular price SARC, LARC=2140 CFA, Sequential recommendation

    Behavioral: Price discounts for LARCs

  • No intervention
    Regular SARC, LARC=5000, Recommendation

    Regular price SARC, LARC=5000 CFA, Sequential recommendation

  • Experimental
    Free SARC, Free LARC, No Recommendation

    Free SARC, Free LARC, Simultaneous recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Free SARC, LARC=500, No Recommendation

    Free SARC, LARC=500 CFA, Simultaneous recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Free SARC, LARC=1000, No Recommendation

    Free SARC, LARC=1000 CFA, Simultaneous recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Free SARC, LARC=2140, No Recommendation

    Free SARC, LARC=2140 CFA, Simultaneous recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Free SARC, LARC=5000, No Recommendation

    Free SARC, LARC=5000 CFA, Simultaneous recommendation

    Behavioral: Price discounts for SARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Regular SARC, Free LARC, No Recommendation

    Regular Price SARC, Free LARC, Simultaneous recommendation

    Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Regular SARC, LARC=500, No Recommendation

    Regular Price SARC, LARC=500 CFA, Simultaneous recommendation

    Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Regular SARC, LARC=1000, No Recommendation

    Regular Price SARC, LARC=1000 CFA, Simultaneous recommendation

    Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Regular SARC, LARC=2140, No Recommendation

    Regular Price SARC, LARC=2140 CFA, Simultaneous recommendation

    Behavioral: Price discounts for LARCs · Behavioral: Sequential vs. simultaneous recommendations

  • Experimental
    Regular SARC, LARC=5000, No Recommendation

    Regular Price SARC, LARC=5000 CFA, Simultaneous recommendation

    Behavioral: Sequential vs. simultaneous recommendations

Interventions

  • BehavioralPrice discounts for SARCs

    SARCs are offered free to the client

  • BehavioralPrice discounts for LARCs

    LARCs are offered at lower prices to the client

  • BehavioralSequential vs. simultaneous recommendations

    Top ranked methods are presented to the client sequentially or simultaneously

06

What researchers measure

Primary outcomes

  1. The client adopted a LARC

    using data from the counseling sessions

    Time frame: 1-day

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

    using data from the counseling sessions

    Time frame: 1-day

Secondary outcomes

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

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

    Time frame: 2-weeks

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

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

    Time frame: 2-weeks

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

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

    Time frame: 2-weeks

  4. Client satisfaction with adopted contraceptive method

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

    Time frame: 2-week and 16-week measurements

  5. Discontinuation of adopted contraceptive method

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

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

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

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

    Time frame: 16-week and 52-week measurements

07

Study locations

1 site
  • Hôpital gynéco-obstétrique et pédiatrique de Yaoundé (HGOPY)
    Yaoundé, Cameroon
08

References and documents

Individual participant data

Plan to share: Undecided — We will likely share de-identified anonymous participant data publicly after the trial ends and our analyses are completed.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03733678
Lead sponsor
World Bank
Collaborators
Stanford University, George Washington University, University of Exeter, University of California, San Diego, Yaounde Gynecology, Obstetrics and Pediatrics Hospital
Responsible party
Berk Ozler (Principal Investigator, World Bank) — Principal investigator
First posted
Nov 7, 2018
Start date
Mar 23, 2021
Primary completion
Dec 31, 2022
Completion
Dec 31, 2024
Last update
May 14, 2025

Study contacts

Berk Ozler, PhD
principal investigator · World Bank

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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