DTP Vaccine Series Completion Clinical Trial
Official title:
Khushi Baby (KB): Efficacy and Impact Assessment of Novel Mobile Health Solution for Vaccination Record Keeping in Rural Udaipur, Rajasthan, India
| Verified date | August 2015 |
| Source | Khushi Baby Inc. |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | India: Institutional Review Board |
| Study type | Interventional |
This is a three arm cluster randomized controlled trial where the unit of randomization is
the immunization camp. Immunization camps are the sole provider of vaccinations in our study
area and have catchment areas of several villages. The 96 immunization camps will be
randomized evenly to one of three arms:
1. control arm; where near field communication (NFC) stickers will be placed on existing
immunization booklets. These stickers can be scanned using a mobile phone with an
installed application whereby information can be entered onto the phone and then
scanned onto the sticker
2. pendant only; where the same NFC technology will be placed into a pendant that is worn
by the infant, and
3. pendant as described above with voice reminders sent 15 days, 1 day prior, and the day
of the scheduled immunization camp dates.
| Status | Enrolling by invitation |
| Enrollment | 300 |
| Est. completion date | April 2016 |
| Est. primary completion date | April 2016 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 42 Days to 6 Months |
| Eligibility |
Inclusion Criteria: - Mother/ Primary Caregiver has an infant between the age of 42 days (minimum age for DTP1 administration per WHO guidelines) and 6 months of age; there is no age restriction for inclusion. In the very rare instance that a male is the primary caregiver, they will also be invited to participate in the study. Survey questions are not gender or age specific, but wil require the caregiver to answer questions about his/her children, socioeconomic and health status, and vaccine awareness. - Self-identified resident within one of the villages associated with the immunization camp - Willing to give informed consent (sign or thumbprint) Exclusion Criteria: - Infant has received at least 1 dose of DTP vaccine - Caregiver and infant intends to move before the next 6 camps have been completed (in the next 6-9 months) |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Khushi Baby Inc. | Indian Institute of Health Management Research (IIHMR), Johns Hopkins Bloomberg School of Public Health, Seva Mandir, India |
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* Note: There are 18 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | 20% increase in DTP3 coverage | Comparing necklace (with or without voice call reminders) to control arm infants | 6 camps after DTP1 receipt (6 months) | No |
| Secondary | Increase in DTP3 coverage for necklace + voice reminder arm compared to other 2 arms | 6 camps after DTP1 receipt (6 months) | No | |
| Secondary | Improved camp attendance rates | Comparing camps randomized to receive necklace (with or without voice reminders) to control arm infants. | Over 6 camp period after DTP1 receipt (6 months) | No |
| Secondary | Retention of pendant compared to that of NFC stickered MAMTA card | 6 camps after DTP1 receipt (6 months) | No | |
| Secondary | Increased time efficiency of NFC system (both stickers and pendants) compared to existing paper-based system of recording immunization | The surveyor will categorize the times separately for new and follow-up patients. The analysis will consider average times for new registrants and follow up registrants in KB app vs. logbook for each health worker (GNM). These indicators will be used to compile a composite measure of time efficiency. | Paper log books (status quo control) will be used to establish a baseline for timeliness during first 2 months of the study. In the latter 2 months, the KB app digitization will be timed. | No |
| Secondary | Increased accuracy between NFC system (both stickers and pendants) compared to existing paper-based system of recording immunization | At the end of each camp the number of child-specific syringes and complete vaccine vials will be counted by the Surveyor; these will serve as the gold standards. The analysis will examine the frequency of underreporting and overreporting of total vaccines (as determined by syringes) and of individual vaccines (as determined by complete vaccine vials when available); rates of underreporting and overreporting will be examined at the camp level (n=2 for each camp) and after clubbing all camps per month (n= 2 months). These indicators will be used to compile a composite accuracy outcome measure. | In the first 2 months, the logbook records will be digitized and de-identified for each camp. In the latter 2 months, the digitization of records will take place exclusively through the KB app. | No |
| Secondary | Survey-based outcomes: user satisfaction, socio-demographic profile of infants, vaccine awareness of mothers and the differential effects on vaccination adherence | Intake survey at enrollment + follow-up surveys at each camp (approximately once a month during follow-up period) | No | |
| Secondary | Failure rate of the Khushi Baby mobile application | time series data to be collected from the app itself (error logs and internal counters for each replacement); number of entries in backup logbook will be digitized and added | Throughout study period of 9 months | No |