MINT-II: Chanjo Kwa Wakati - Improving Vaccination Coverage and Timeliness in Rural Settings

Sponsor
University of South Carolina (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06024317
Collaborator
Duke University (Other), Emory University (Other), University of North Carolina (Other), National Institute for Medical Research, Tanzania (Other)
1,200
1
2
40.9
29.3

Study Details

Study Description

Brief Summary

Background and Objective:

Tanzania is one of 20 countries where the majority of un- and under-vaccinated children reside. Prior research identified substantial rural-urban disparities in rates and timeliness of childhood vaccination in Tanzania, with children in rural settings being more like to receive delayed or no vaccinations. This type 1 effectiveness implementation hybrid study will evaluate the effect of Chanjo Kwa Wakati ("Timely Vaccination" in Kiswahili), a community-based, integrated digital health intervention, on vaccination timeliness. The intervention combines a vaccination knowledge intervention, mobile phone-based reminders, and incentives with the goal to promote timely childhood vaccinations.

Methods:

The study will be conducted in two predominantly rural regions in Tanzania with high numbers of un- or under-vaccinated children. Forty rural health facilities and their catchment areas ("clusters") will be randomized to an early or delayed onset study arm. From each cluster, three cohorts of mother-child dyads, one retrospective cohort and two prospective cohorts, will be enrolled into the study. For all vaccines due during the first year of life, timeliness (primary outcome) and coverage (secondary outcome) will be observed for 1200 children (600 intervention children and 600 non-intervention children). Study logs, fidelity checklists, quantitative surveys, vaccination records, and qualitative interviews with mothers and key informants will be used to inform the five constructs of the Reach, Effectiveness, Adoption, Implementation and Maintenance (RE-AIM) framework. Results will be used to develop an implementation blueprint that can guide future adaptations, sustainability, and scale-up of Chanjo Kwa Wakati.

Hypothesis:

The hypothesis is that Chanjo Kwa Wakati is effective for increasing the timeliness of childhood vaccinations due by age 1 year compared to the standard of care.

Expected impact:

This study will address the lack of rigorous evidence on the effectiveness of an community-based digital health intervention for promoting vaccination coverage and timeliness among children from sub-Saharan Africa, and identify implementation strategies to facilitate the deployment of integrated vaccination interventions in low- and middle-income country settings.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Chanjo Kwa Wakati - Knowledge Intervention
  • Behavioral: Chanjo Kwa Wakati - Reminders
  • Behavioral: Chanjo Kwa Wakati - Incentives
  • Behavioral: Chanjo Kwa Wakati - Service notifications
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This type 1 effectiveness-implementation hybrid study uses a cluster-randomized trial design to evaluate intervention effectiveness.This type 1 effectiveness-implementation hybrid study uses a cluster-randomized trial design to evaluate intervention effectiveness.
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
"Chanjo Kwa Wakati" - Leveraging Community Health Workers and a Responsive Digital Health System to Improve Vaccination Coverage and Timeliness in Rural Settings
Anticipated Study Start Date :
Feb 1, 2024
Anticipated Primary Completion Date :
Jun 30, 2027
Anticipated Study Completion Date :
Jun 30, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Early onset

20 clusters will be assigned to the early onset arm. A cross-sectional cohort and two longitudinal cohorts will be enrolled from each cluster. Both longitudinal cohorts will receive all components of the Chanjo Kwa Wakati intervention.

Behavioral: Chanjo Kwa Wakati - Knowledge Intervention
Counseling scripts assessing and addressing vaccination-related knowledge gaps

Behavioral: Chanjo Kwa Wakati - Reminders
Reminders of upcoming vaccination due dates, sent to the mother's mobile phone

Behavioral: Chanjo Kwa Wakati - Incentives
Conditional incentives for timely vaccination, tailored to each child's vaccination schedule

Behavioral: Chanjo Kwa Wakati - Service notifications
Service notifications (e.g., related to stockouts or service non-availability), sent to the mother's mobile phone

Experimental: Delayed onset

20 clusters will be assigned to the delayed onset arm. A cross-sectional cohort and two longitudinal cohorts will be enrolled from each cluster. The second longitudinal cohort will receive all components of the Chanjo Kwa Wakati intervention.

Behavioral: Chanjo Kwa Wakati - Knowledge Intervention
Counseling scripts assessing and addressing vaccination-related knowledge gaps

Behavioral: Chanjo Kwa Wakati - Reminders
Reminders of upcoming vaccination due dates, sent to the mother's mobile phone

Behavioral: Chanjo Kwa Wakati - Incentives
Conditional incentives for timely vaccination, tailored to each child's vaccination schedule

Behavioral: Chanjo Kwa Wakati - Service notifications
Service notifications (e.g., related to stockouts or service non-availability), sent to the mother's mobile phone

Outcome Measures

Primary Outcome Measures

  1. Penta 3 delay in days (continuous) [Assessed during the endline survey, an average follow-up period of 1 year]

    The average number of days between the Penta3 vaccination due date (at age 14 weeks) and the date on which the child received the vaccination. Dates abstracted from the child's immunization card.

Secondary Outcome Measures

  1. Penta 3 delay > 28 days (binary) [Assessed during the endline survey, an average follow-up period of 1 year]

    The percentage of participants with a delay >28 days between the Penta 3 vaccination due date (at age 14 weeks) and the date on which the vaccination was received. Dates abstracted from the child's immunization card.

Other Outcome Measures

  1. Penta 3 coverage (binary) [Assessed during the endline survey, an average follow-up period of 1 year]

    The percentage of children who received the Penta 3 vaccination. Coverage abstracted from the child's immunization card.

  2. Coverage of all recommended vaccines (binary) [Assessed during the endline survey, an average follow-up period of 1 year]

    The percentage of children who received all vaccines recommended by age 1 year. Coverage abstracted from the child's immunization card.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria for the Cross-sectional sample:
  • mothers of children ages 12-23 months

  • residing in the sampling area

Inclusion Criteria for the Longitudinal sample:
  • pregnant women in their last trimester of pregnancy

  • residing in the sampling area

  • expected to reside in the sampling area until the child reaches age 1 year

Exclusion Criteria:
  • Women who are not living in catchment areas of participating health facilities (which routinely provide maternal and child health services, including antenatal care and at least weekly routine childhood immunization. Facilities must be operational, must have at least 2 community health workers, and must have reported at least 100 pregnancies or births in the year prior to study implementation.)

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Institute for Medical Research Dar Es Salaam Tanzania

Sponsors and Collaborators

  • University of South Carolina
  • Duke University
  • Emory University
  • University of North Carolina
  • National Institute for Medical Research, Tanzania

Investigators

  • Principal Investigator: Jan Ostermann, PhD, University of South Carolina

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jan Ostermann, Associate Professor, University of South Carolina
ClinicalTrials.gov Identifier:
NCT06024317
Other Study ID Numbers:
  • Pro00120675
First Posted:
Sep 6, 2023
Last Update Posted:
Sep 11, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jan Ostermann, Associate Professor, University of South Carolina

Study Results

No Results Posted as of Sep 11, 2023