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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03163524
Other study ID # 007-15
Secondary ID
Status Recruiting
Phase N/A
First received July 18, 2016
Last updated June 9, 2017
Start date March 2016
Est. completion date September 2017

Study information

Verified date June 2017
Source Marie Stopes International
Contact Olivia Nuccio, MSc
Email olivia.nuccio@mariestopes.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date September 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Uganda Marie Stopes Uganda call centre Kampala

Sponsors (3)

Lead Sponsor Collaborator
Marie Stopes International ideas42, Marie Stopes Uganda

Country where clinical trial is conducted

Uganda, 

Outcome

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