MedPath

mHealth to Increase Measles Immunization - a Randomized Controlled Trial in Guinea-Bissau

Not Applicable
Conditions
Measles
Interventions
Other: SMS reminder message
Other: Voice call + SMS message
Registration Number
NCT02662595
Lead Sponsor
Bandim Health Project
Brief Summary

The question that this project seeks to answer, is whether mobile phones can be used to increase the measles vaccination coverage and timeliness in Guinea-Bissau. The intervention will be evaluated in terms of direct health outcomes and cost/benefit analysis, generating evidence that could help policy makers making informed decisions about implementing mHealth interventions at a national level.

The intervention takes the form of a randomized controlled trial in which text messages (SMS) as well as voice calls are scheduled and delivered to mo thers to remind and encourage them to have their children timely vaccinated against measles. In addition, the messages will include relevant information about opening hours and availability of the measles vaccine at the mothers' local health facilities thus improving coordination. The trial will include three different randomization groups with approx. 350 participants in each group. The first group will receive SMS messages, the second group will receive a voice call in addition to the SMS messages, and the third group is a control group that does not receive any intervention.

Study participants will be enrolled following birth at one of three health centers in different rural regions of Guinea-Bissau. Before the measles vaccine is scheduled to be given, at 9 months of age, mothers will receive the intervention message depending on their assigned randomization group. When the measles vaccine is administered, the child will be registered as having received the measles vaccination.

A follow-up phone interview will be conducted at 12 months of age for all children participating regardless of randomization group and whether or not they received the measles vaccine. All participating children, who at that time still have not received the measles vaccine, will be offered the vaccine at the expense of the project.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
1050
Inclusion Criteria
  • the mother has access to a cell phone (either her own phone or the phone of a household member)
  • the mother lives in the uptake area of the health center.
Exclusion Criteria
  • the mother does not have access to a mobile phone.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Text messageSMS reminder messageSubjects in this arm will receive a text message reminder in due time for measles vaccination.
Text message and voice callVoice call + SMS messageSubjects in this arm will receive a voice call in addition to a text message reminder in due time for measles vaccination.
Primary Outcome Measures
NameTimeMethod
MV Coverage at 12 months of age12 months of age

Difference in measles vaccination coverage at 12 months of age between the intervention and the control groups.

Secondary Outcome Measures
NameTimeMethod
Average number of visitsAt 12 months

Average number of visits to the health center with the purpose of receiving MV needed before MV is successfully administered.

TimelinessAt 12 months

Difference in timeliness of measles vaccines administered, measured as median age of measles vaccinated children.

Trial Locations

Locations (3)

Varela Health Center

🇬🇼

Varela, Cacheu, Guinea-Bissau

Catio Health Center

🇬🇼

Catío, Tombali, Guinea-Bissau

Paunca Health Center

🇬🇼

Paunca, Gabú, Guinea-Bissau

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