Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
1445 participants
INTERVENTIONAL
2017-07-19
2018-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This study proposes to develop and test two types of silicon bracelets for children to stimulate immunization demand and simultaneously address supply side verification issues. These bracelets use a combination of numbers and symbols to denote the age of the child and due vaccines and are designed for illiterate or uneducated mothers; are low-cost and adaptable to most local settings. At the time of vaccine administration, the appropriate symbol denoting the vaccine on the bracelets is punched and therefore the bracelets can serve as effective reminders for mothers for timely immunization of their child and as a tool for vaccinators to verify vaccine administration and coverage.
An individually randomized, three-arm parallel group design randomized control trial will be conducted with equal allocation in the two treatment groups and control group. Children in intervention group A will receive the simple silicon bracelets, children in intervention group B will receive the bracelets developed by Alma Sana Inc. and children in the Control group will not receive any intervention. The impact of these immunization reminder bracelets on immunization coverage and timeliness will be evaluated through a randomized control trial (RCT) across 4 immunization centers in Karachi. To evaluate the bracelets' impact, variables of interest-coverage and timeliness rates of pentavalent-3/PCV-3/polio-3 and Measles 1 vaccine will be compared between Group A and the Control Group and Group B and the Control Group.
Proposed results include increase in immunization coverage and timeliness of Pentavalent-3/Pneumococcal Conjugate Vaccine (PCV-3)/Polio-3 and Measles-1 in the intervention versus control group.
The study will provide evidence of the bracelet's effectiveness for the global health community and provide a simple tool for strengthening routine immunization efforts in Pakistan.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Use of SMS and Interactive Reminders to Improve Timely Immunization Coverage
NCT03379467
Long-term Immunogenicity of L-HAV Vaccine Among Healthy Thai Children and Adolescents
NCT07032610
Khushi Baby (KB): Novel Mobile Health Solution for Vaccination Record Keeping in India
NCT02518178
Typhoid Conjugate Vaccine Trial Among Children Younger Than 2 Years in Ouagadougou, Burkina Faso
NCT03614533
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
NCT01878435
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
An individually randomized, three-arm parallel group design randomized control trial will be conducted with equal allocation to evaluate the impact of the Alma Sana bracelet and simple silicon bracelet by comparing the variables of interest (coverage and timeliness rates of (pentavalent-3/PCV-3/polio-3 and Measles 1) between treatment groups and the Control Group.
Study Procedures:
A consent form will be used to seek consent from caregivers accompanying the child to screen the child for the study. Among those who provide consent, a screening form will be used to identify the eligible participants. After screening, seeking consent from primary caregivers (mother and/or father) they will be randomized into the treatment groups (to receive the bracelet) or to serve as a control. The randomization sequence will be created using Stata version 13 with a 1:1:1 allocation using random block sizes of 3, 6, 9 and 12. The allocation sequence will be concealed from the study staff responsible for screening and enrolling participants in serially numbered, opaque, sealed envelopes. After randomization, each child will be assigned a unique study ID (a sticker containing the study ID will be pasted on the child's government issued EPI card).
Details of the procedures in the intervention and control groups are outlined below:
Intervention group A and B: Children in both the intervention groups (A and B) will receive the two different bracelets to be placed on the child's wrist. Additionally, mothers will be provided instructions explaining the use of the bracelet and helping them decode the symbols to enable them to use the bracelet to remind themselves of their child's vaccinations. Children will receive the scheduled EPI vaccine by the vaccinator who will then punch a hole in the child's bracelet to denote vaccine administration. The child's vaccine data will be recorded in the EPI card and EPI register as per routine.
All participants (irrespective of whether they are in the treatment group A or B or control group) will receive the routine EPI vaccinations as per Pakistan's EPI Immunization schedule (one dose of BCG and polio soon after birth, 3 doses of Pentavalent/Polio/PCV at 6, 10 and 14 weeks, and 2 doses of Measles vaccine and 9 and 15 months of age) and the vaccinator will record the child's immunization data in the EPI immunization card as well as EPI register. The difference between the intervention and standard care is only the provision of bracelets which provide an additional source (apart from the EPI cards) to record and track vaccinations.
Control group: Children in the control group will receive the scheduled EPI vaccine from the vaccinator. The child's vaccine data will be recorded in the EPI card and register as per routine.
Data collection will be done using the following documents over 5 total visits:
1. Enrollment Form: At the child's first visit to the center, the field worker will note the name and age of the child along with the immunizations received during the visit in addition to basic demographic information in the enrolment form. This information, along with basic biographic information is recorded routinely by vaccinators in their government issued permanent medical registers. An immunization visit typically takes between 10 and 15 minutes, not including any time spent waiting to be seen by the vaccinator.
2. Follow-up Form: For the follow up visits by the caregivers to get the subsequent vaccinations (3 - 4 visits), field workers will be based at the participating EPI centers throughout the follow-up period. Each follow-up visit takes about 10-15 minutes of the caregivers time, not including any time spent waiting to be seen by the vaccinator. Each child in the study is provided a unique EPI number by the EPI staff as per routine and also a study ID by a field worker. The linkage between the EPI number and the ID number will be maintained after data collection is complete. The field workers will use these IDs to identify the study participants when they come for follow-up visits. At each follow up visit, the field worker will record the vaccine administered and date for each child in the study, including verifying data on past immunizations and due vaccines (follow-up form attached). Therefore, for each study participant, the field workers would collect data 3-4 times during the follow-up period. The minimum duration of follow up provided to each participant will be until the child receives Measles-1 vaccine (given at 9 months of age per WHO recommendations). The maximum duration of follow up provided to each participant will be 11 months.
3. Completion Form: After the completion of follow-up period, short (15-20 minutes) phone or in-person interviews will be conducted to collect follow up vaccination data (if missing) and data on experiences of study participants regarding the bracelets (completion form attached). Phone numbers and addresses are provided as part of the Enrollment form. It is culturally acceptable for in person interviews to be conducted in their home. Key data points would include reasons for drop-outs, whether mothers understood how to use the bracelets, how often mothers said their babies wore the bracelets and why, what mothers liked and disliked about the bracelets and whether mothers would continue using the bracelets as reminders moving forward.
Statistical analysis plan:
Intention to treat analysis will be used-that is, all subjects will be analysed with the assumption that they remained in the treatment group to which they were initially assigned.
Y=c+β1T1+β2T2+γX+ε
Y is the relevant outcome measure (for instance Penta-3 coverage) C is the constant that gives the value of the outcome for the control group T1 and T2 are treatment dummy variables for group 1 (Alma Sana bracelets) and group 2 (Simple silicon bracelets) β1 and β2 will provide the difference in outcome variable between treatment one and the control group and treatment 2 and the control group respectively X is the set of possible covariates (gender, mother's education)
Logistic regression will be used to determine whether the difference in outcome between the two treatment groups and control group are statistically significant and whether the difference in outcome between the two treatment groups is statistically significant from each other.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Alma Sana Bracelet Arm
Subjects in this arm will receive a vaccine reminder and tracker bracelet developed by Alma Sana Inc. This bracelet uses a combination of symbols and numbers to denote the entire vaccine schedule a child is supposed to receive before the age of 2 years. Shapes indicate vaccines, and numbers signify the child's age.
Alma Sana Bracelet
Every time a child receives a vaccine, vaccinators will hole punchers to perforate shapes denoting the particular vaccine a child has received.
Simple Silicon Bracelet Arm
Subjects in this arm will receive a simple silicon bracelet. This bracelet has six symbols to remind parents that their child needs to get at least six vaccination visits before he reaches 2 years of age. The first five symbols are represented by a crescent shape and the sixth symbol is represented by a star shape to denote that the child is fully immunized.
Simple Silicon Bracelet
Every time a child receives a vaccine, vaccinators will hole punchers to perforate shapes denoting the particular vaccine a child has received.
Control Arm
Subjects in this arm will not receive any bracelet/intervention.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Alma Sana Bracelet
Every time a child receives a vaccine, vaccinators will hole punchers to perforate shapes denoting the particular vaccine a child has received.
Simple Silicon Bracelet
Every time a child receives a vaccine, vaccinators will hole punchers to perforate shapes denoting the particular vaccine a child has received.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Child is healthy
3. Child's caregiver has been a resident of study area for more than 6 months
4. Child is accompanied by a primary caregiver (mother and/or father)
Exclusion Criteria
2. Parents plan to go to a different center for completing the vaccination course
3 Months
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Harvard Medical School (HMS and HSDM)
OTHER
Interactive Research and Development
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Danya Arif
Program Manager
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Danya A Siddiqi, MSc
Role: PRINCIPAL_INVESTIGATOR
Interactive Research and Development
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Future Colony
Karachi, Sindh, Pakistan
KMC Maternity Home
Karachi, Sindh, Pakistan
MCH-36B
Karachi, Sindh, Pakistan
Urban Health Center
Karachi, Sindh, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Siddiqi DA, Ali RF, Munir M, Shah MT, Khan AJ, Chandir S. Effect of vaccine reminder and tracker bracelets on routine childhood immunization coverage and timeliness in urban Pakistan (2017-18): a randomized controlled trial. BMC Public Health. 2020 Jul 11;20(1):1086. doi: 10.1186/s12889-020-09088-4.
Siddiqi DA, Munir M, Shah MT, Khan AJ, Chandir S. Effect of vaccine reminder and tracker bracelets on routine childhood immunization coverage and timeliness in urban Pakistan: protocol for a randomized controlled trial. BMC Public Health. 2019 Oct 30;19(1):1421. doi: 10.1186/s12889-019-7667-3.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
027562-746846- 0303
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.