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N/A N=608 Randomized Single-blind Health Services Research

Enhancing Health Care Access With Cellular Technology

Vaccination

Enrolled (actual)
608
Serious AEs
0.0%
Results posted
Jun 2018
Primary outcome: Primary: Immunization Rate — 41.7; 40.1; 50.0 Percentage of immunizations

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Reminders alone (Behavioral); Compliance-linked incentives (Behavioral)
Age
Pediatric
Sex
All
Sponsor
Johns Hopkins University
Primary completion
Jul 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Immunization Rate
41.7; 40.1; 50.0
SECONDARY
Timeliness of Vaccinations
31.6; 24.7; 40.8

Summary

Despite the impressive economic progress in developing countries, significant proportion of young children and pregnant women living in low-resource settings remain inadequately immunized. Progressive decline in immunizations are in large part attributable to poor follow-up and compliance. National and international pediatric bodies, recommend a time sensitive schedule for childhood immunizations, boosting immunity with each subsequent cycle, leading to adequate levels of immune protection. Due to inadequate protective immunity, resulting from poor vaccination compliance, outbreaks of vaccine-preventable diseases are rampant, making childhood mortality in this group among the highest in the world. Major challenges of vaccination programs include maintaining / tracking records, linked to positive identification of individual children, and strategies to improve follow-up and compliance. Novel cellular technology based approaches targeting behavior modifications can therefore significantly impact health outcomes in these communities. In this proposal, the investigators will evaluate a novel software platform, utilizing biometric identification of subjects, paired with cell-phone reminders and compliance-linked incentives to improve uptake and coverage of primary vaccinations in young children and pregnant women.

Eligibility Criteria

Inclusion Criteria

Mother-child (or caregiver-child) units with child <2 years of age OR Pregnant women

Exclusion Criteria

Family does not have cell-phone OR cannot provide informed consent

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03180138). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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