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Clinical Trials/NCT01878435
NCT01878435CompletedNot Applicable

Randomized Controlled Trial of the Impact of Mobile Phone Delivered Reminders and Travel Subsidies to Improve Childhood Immunization Coverage Rates and Timeliness in Western Kenya

Johns Hopkins Bloomberg School of Public Health1 site in 1 country2,018 target enrollmentStarted: October 1, 2013Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
2,018
Locations
1
Primary Endpoint
Percent of children immunized

Study Overview

Brief Summary

The project goal is to conduct a randomized controlled trial (RCT) to test whether mobile phone short message system (SMS) reminders, either with or without mobile-phone based travel subsidies will improve timeliness, coverage, and drop-out rates of routine EPI vaccines in rural western Kenya.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
0 Weeks to 5 Weeks (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Mother of infant aged 0-4 weeks during the study period
  • Current resident of one of the study villages
  • Willing to sign informed consent for the study

Exclusion Criteria

  • Plans to move out of the study area in the next 6 months
  • Resides in a village with active immunization intervention/program
  • Has already received immunizations other than birth dose of BCG or polio

Arms & Interventions

SMS reminder

Experimental

Intervention: SMS reminder (Other)

SMS reminder and Travel subsidy

Experimental

Intervention: Travel subsidy (Other)

SMS reminder and Travel subsidy

Experimental

Intervention: SMS reminder (Other)

Control

No Intervention

SMS reminder and Travel subsidy 2

Experimental

Intervention: SMS reminder (Other)

SMS reminder and Travel subsidy 2

Experimental

Intervention: Travel subsidy 2 (Other)

Outcomes

Primary Outcomes

Percent of children immunized

Time Frame: Up to 12 months of age

Secondary Outcomes

  • Percent of fully immunized children (FIC) by study arm(10 months of age)
  • Proportion of children vaccinated by study arm(Within 2 weeks of each scheduled vaccine date)
  • Vitamin A coverage, o evaluate if the interventions had impact on other indicators of health status(Age 12 months)
  • Height-for-age,to evaluate if the interventions had impact on other health status indicators(Age 12 months)
  • Proportion of children dropping out between doses(Age 24 weeks)
  • Direct costs for each intervention arm(25 months, approximate time period for deploying interventions)
  • Proportion of children receiving measles and pentavalent vaccines by study arm(Age 24 weeks (pentavalent only), 10 months and age 12 months)
  • Proportion in each arm vaccinated by mobile phone ownership and by residential distance from a health facility(Age 12 months)
  • Bed-net usage, to evaluate if the interventions had impact on other indicators of health status(Age 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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