Behavioural Insights to Improve Take up of SRH Services (Uganda)

Applying Behavioural Insights to Improve Take up of Sexual and Reproductive Health Services

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03163524

Enrollment

2000

Registered

2017-05-23

Start date

2016-03-31

Completion date

2017-09-30

Last updated

2017-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Behavior

Keywords

family planning, reproductive health, m-health

Brief summary

This is a randomised controlled trial to test the impact of a modified e-coupon service, delivered through SMS, on uptake of sexual and reproductive health services among women calling a free hotline in Uganda.

Detailed description

The overall goal of the proposed research project is to increase uptake of sexual and reproductive health (SRH) services among clients who call into Marie Stopes Uganda's free hotline. The study seeks to achieve this goal by using behavioural economics to design interventions to increase redemptions of e-coupons distributed to hotline clients. The intervention will include modifying the text message sent to e-coupon recipients as well as sending follow-up texts reminding clients to use their coupons. The impact of the intervention will be evaluated using a randomized controlled trial (RCT). The intervention will be implemented and data will be collected regularly over a period of approximately 12 months. Strict confidentiality procedures in line with Marie Stopes International's best practices will be put into place to ensure that information made public or otherwise distributed outside the principle investigators and other key personnel cannot be linked to any individual respondents. Results from the study will be published in a report, among other outputs, and the outcomes will be shared within MSI as well as with the wider SRH community.

Interventions

OTHERe-Coupon Text Modification and Reminders

The treatment group will receive a modified text of the current e-coupon. They will also receive notification that they have been enrolled in the study via a second text. They will also receive a series of text message reminders to redeem their e-coupons at intervals of 6, 13 and 18 days after coupon origination.

OTHERe-Coupon standard text

Participants receive control text (SMS) message, which contains a numeric coupon code and no additional text to the standard coupon.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

SINGLE (Caregiver)

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Callers to the call centre who are over the age of 18, receive an e-coupon, and consent to participate in the research.

Exclusion criteria

* Callers who are below the age of 18, non-recipients of e-coupons, and those who receive e-coupons but do not consent to participate in the study.

Design outcomes

Primary

Measure	Time frame	Description
Increase in e-coupon redemption in MSU centres	6 months	Increase in proportion of e-coupons redemmed in MSU centres within 6 months of intervention
Increase in SRH service uptake in MSU centres	6 months	Increase in the proportion of participants taking up an SRH service (of any kind) in an MSU centre within 6 months

Countries

Uganda

Contacts

Primary ContactOlivia Nuccio, MSc

olivia.nuccio@mariestopes.org

Backup ContactKathryn Church, PhD

kathryn.church@mariestopes.org

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026