Evaluation of an Infant Immunization Encouragement Program in Nigeria
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03870061 |
Recruitment Status :
Completed
First Posted : March 11, 2019
Last Update Posted : March 31, 2020
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Tuberculosis Diphtheria Tetanus Pertussis Hepatitis B Haemophilus Influenzae Type b Infection Pneumonia, Bacterial Measles Rotavirus Infections Polio Yellow Fever | Behavioral: All Babies Are Equal Initiative (conditional cash transfer program) | Not Applicable |
The study will be structured as a two-arm cluster RCT with clinics catchment areas as clusters. One arm will serve as the control (83 clinics) and will operate as the status quo, while the other arm will receive New Incentives' full program (84 clinics). This design will measure the causal effect of New Incentives' program on the likelihood of an infant receiving a vaccine. The unit of treatment and randomization is the clinic catchment, while the unit of measurement for the key outcomes is the individual infant.
Eligible caregivers who bring their infant(s) to a treatment group health facility for immunizations are first enrolled in the program by New Incentives staff, who record caregiver and infant details. If the child has received the vaccination, the caregiver receives the cash incentive, and instructions on when to return for the next vaccination and incentive payment.
Data collection of outcome measures takes place at three points (baseline, midline, and endline) using a series of self-reported surveys of caregivers, examination of the child's health card (where available) and reviewing clinic records. Baseline was completed between August and October 2017, midline is scheduled for March 2019, and endline is planned for November 2019 to January 2020. Across all outcome measurements, sampled infants will be aged between 12 and 16 months (though baseline surveyed some infants aged up to 24 months to increase sample size). These age groups are sampled as they are well beyond the age at which children should receive the program vaccinations. (The Nigerian Routine Immunization schedule aims to give the program vaccinations between birth and 9 months old.) IDinsight does not follow the same infants from baseline to midline to endline but, rather, compares coverage rates in the same age group at each point in time. From the perspective of the participant, taking part in the study involves receiving a researcher into their home, providing informed consent, and answering a 1-hour survey.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 5187 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | The study will be structured as a two-arm cluster RCT. One arm (83 clinics) will serve as the control and will operate as the status quo, while the other arm (84 clinics) will receive New Incentives full program. This design will measure the causal effect of New Incentives' program on the likelihood of an infant receiving a vaccine. New Incentives, an international non-governmental organization (NGO), is addressing the apparent shortfall in demand for immunization by offering cash incentives to caregivers for bringing their child to clinics for the first five visits of the Nigerian Routine Immunization schedule. To be eligible, the child must reside in the catchment area of the clinic and fall within the age range targeted for the vaccination in question. Infants do not need to have received the previous vaccine in the schedule to be eligible. Incentives are paid in cash by a New Incentives staff member who also ensures the infant meets the eligibility criteria outlined above. |
Masking: | None (Open Label) |
Masking Description: | Potential participants in treatment communities likely interact with implementing staff (either to receive the program, or in passing). Potential participants in control communities usually only interact with data collection staff. They are informed about the studies' general goals. |
Primary Purpose: | Prevention |
Official Title: | Randomized Evaluation of a Conditional Cash Transfer Program for Routine Immunizations of Infants in Nigeria |
Actual Study Start Date : | July 1, 2018 |
Actual Primary Completion Date : | February 20, 2020 |
Actual Study Completion Date : | February 20, 2020 |

Arm | Intervention/treatment |
---|---|
No Intervention: Control | |
Experimental: Treatment
This arm receives the full New Incentives' conditional cash transfer program (All Babies Are Equal Initiative).
|
Behavioral: All Babies Are Equal Initiative (conditional cash transfer program)
New Incentives, an NGO, offers cash incentives to caregivers for bringing their child to clinics for the first five visits of the Nigerian Routine Immunization schedule. These small cash transfers can provide some material benefit to new caregivers from poor communities. At a minimum, they help offset time and transport costs. The following vaccines are directly incentivized by the New Incentives' program: tuberculosis (BCG vaccine); diphtheria, tetanus, pertussis, hepatitis B and Haemophilus influenzae Type B (Pentavalent Vaccine), pneumococcal bacteria (PCV vaccine), measles vaccine. |
- The probability that a 12- to 16-month-old in a community served by a study clinic received BCG (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The probability that a 12- to 16-month-old in a community served by a study clinic received at least one dose of PENTA (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The probability that a 12- to 16-month-old in a community served by a study clinic received Measles 1 (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The probability that a 12- to 16-month-old in a community served by a study clinic is fully immunized (loose and strict) (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The timeliness of vaccination, particularly for Measles 1, among 12- to 16-month-olds in communities served by a study clinic (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The average number of vaccines received per 12- to 16-month-old child in communities served by a study clinic (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The percentage of 12- to 16-month-olds in communities served by a study clinic who received at least one injectable vaccine (based on caregivers' report of their child's vaccination history) [ Time Frame: 12 to 16 months after birth ]
- The probability that a 12 to 16-month old in a community served by a study clinic received at least one dose of PCV? [ Time Frame: 12 to 16 months after birth ]
- The change over time in the volume of BCG, Penta 1, Penta 2, Penta 3, and Measles vaccinations recorded in clinic administrative records between treatment and control [ Time Frame: 12 to 16 months after birth ]

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 12 Months to 16 Months (Child) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Children aged 0 to 16 months can be enrolled in the program and incentives paid to their caregivers
- Children aged 12 to 16 months will have their data measured at endline
- All participants must reside in study clinic catchment areas.
- Vaccination status will be measured by caregiver survey. Caregivers must consent to the survey
Exclusion Criteria:
- Residence outside the study area (self-reported)
- Outside the age range (self-reported)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03870061
Nigeria | |
Primary Health Care facilities across Jigawa State | |
Various Cities, Jigawa, Nigeria | |
Primary Health Care facilities across Katsina State | |
Various Cities, Katsina, Nigeria | |
Primary Health Care facilities across the Zamfara State | |
Various Cities, Zamfara, Nigeria |
Study Director: | Alison Connor, PhD | IDinsight |
Documents provided by Zack Devlin-Foltz, IDinsight:
Responsible Party: | Zack Devlin-Foltz, Manager, IDinsight |
ClinicalTrials.gov Identifier: | NCT03870061 |
Other Study ID Numbers: |
001 |
First Posted: | March 11, 2019 Key Record Dates |
Last Update Posted: | March 31, 2020 |
Last Verified: | March 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Plan Description: | All participant-level data is anonymized through removing any information that could lead to back-tracking the identity of the respondent - each respondent is allocated a random identification number in place of their name. Anonymized data are currently stored in a password-protected repository on IDinsight's Dropbox site. Access is restricted to IDinsight staff that are on the project. IDinsight and New Incentives collect various clinic-level data as well for use as covariates and to inform operational decisions. These data are stored in the same repositories and in New Incentives' own password-protected internal dashboard. Requests for access to data can be made directly to IDinsight (Manager: Zack Devlin-Foltz (zack.devlinfoltz@idinsight.org) and Corresponding Investigator: Dr. Niklas Heusch (niklas.heusch@idinsight.org)) |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Randomized Controlled Trial Vaccinations Nigeria Conditional Cash Transfers |
Cash Incentives Infants Impact Evaluation Immunization |
Infections Communicable Diseases Hepatitis B Tuberculosis Diphtheria Yellow Fever Pneumonia, Bacterial Rotavirus Infections Haemophilus Infections Disease Attributes Pathologic Processes Hepatitis Liver Diseases Digestive System Diseases Pneumonia |
Respiratory Tract Infections Lung Diseases Respiratory Tract Diseases Blood-Borne Infections Hepadnaviridae Infections DNA Virus Infections Virus Diseases Hepatitis, Viral, Human Mycobacterium Infections Actinomycetales Infections Gram-Positive Bacterial Infections Bacterial Infections Bacterial Infections and Mycoses Gram-Negative Bacterial Infections Corynebacterium Infections |