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Not yet recruiting NCT07510971

mHealth Intervention for Improving Vaccination Coverage in Bangladesh

No phase Interventional mHealth Intervention SMS

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Automated voice reminders with behavior change messages, Text with behavior change message, Control.
Who it may be relevant to
Registry conditions: mHealth Intervention, SMS. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Mobile Health Solutions Combined With Behavior Change Approaches to Improve Vaccination Coverage and Timeliness in Bangladesh: a Cluster Randomized Controlled Trial

Overview

Noncompliance and delay in vaccination have caused millions of preventable deaths worldwide particularly in low-and middle-income countries (LMICs). The main reasons for delay in vaccinations or dropout from vaccination programs are vaccine hesitancy, lack of knowledge, forgetting due date, lack of trust, and religious and social barriers. Recently, various mobile health (mHealth) interventions such as voice call, text message reminders have been implemented in LMICs to improve awareness of vaccine availability and provide timely reminders. However, the implication and impact assessment of mHealth interventions with behavior change message for improving vaccination coverage and timeliness is limited. In this project, a three-armed cluster randomized controlled trial (cRCT) will be conducted to assess the impact and cost-effectiveness of mHealth interventions with behavioral change approach on vaccination coverage and timeliness in Bangladesh. A total of 7800 caregivers of children aged less than 4 weeks will be recruited and randomly allocated equally to each arm: control, voice call, and short message service (SMS) reminders with behavioral change message. The primary outcomes will include coverage of full immunization among children in first year of life, and secondary outcomes will be coverage for each vaccine, timeliness, and infant mortality.

Interventions

  • Behavioral Automated voice reminders with behavior change messages
    An automatic voice call with behavior change messages will be sent on 3 days and one day before the scheduled visit at 6 weeks, 10 weeks, and 14 weeks for the three doses of DPT vaccine and age 9 months for MCV1 vaccine. The reminder will be sent in local language.
  • Behavioral Text with behavior change message
    SMS will be sent on 3 days and one day before the scheduled visit at 6 weeks, 10 weeks, and 14 weeks for the three doses of DPT vaccine and age 9 months for MCV1 vaccine.
  • Other Control
    The participant of the control group will receive only standard care.

Primary outcome measures

  • Full vaccination [Time frame: 1 year]
  • Vaccine Timeliness [Time frame: 1 year]
Secondary outcome measures (2)
  • Vaccination coverage [Time frame: 1 year]
  • Cost-effectiveness of the intervention [Time frame: 1 year after]

Eligibility criteria

Inclusion criteria

  • You are the infant's caregiver (mother, father, or legal guardian).
  • The infant is less than 4 weeks (28 days) old at the time of enrollment.
  • You reside within the jurisdiction of the designated community health center and have no plans to move within the next 12 months.
  • Depending on your assigned group, you can do one of the following:
  • You can read Bengali SMS messages yourself.
  • You can receive support from a family member living with you who reads Bengali aloud.

(Note: For the voice call group, literacy is not an issue.)

  • You understand the content of this study and have completed the required informed consent form.

Exclusion criteria

  • Caregivers of children aged 4 weeks or older at the time of enrollment
  • Children who have received any vaccine other than BCG or polio at birth
  • The caregiver plans to move out of the study area within the next six months.
  • The caregiver does not want to receive the vaccination at the intervention health center.
  • The caregiver (father, mother, or other family member) does not have a phone.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07510971 · C-T2025-0695

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗