Randomized Evaluation of Voucher Interventions for Value and Effectiveness (REVIVE) in Philippines (REVIVE)

June 6, 2026 updated by: Phuong Hong Nguyen, International Food Policy Research Institute

This study aims to evaluate whether revised food voucher programs, combined with nutrition education sessions, can improve food security, dietary quality, nutrition knowledge, and nutritional outcomes among low-income households in the Philippines. Researchers will compare different monthly voucher amounts-Philippine Peso (PhP) 3,000, PhP 5,000, and PhP 8,000-with a no-voucher control group to determine which approach is most effective.

The main questions the study aims to answer are:

  • Do food vouchers improve household food security, reduce hunger, and improve dietary quality and nutrient intake?
  • Do larger voucher amounts lead to greater improvements in nutrition and health outcomes?
  • Does enhanced nutrition education improve nutrition knowledge and healthy eating practices?

Participants will:

  • Receive either a monthly food voucher or no voucher, depending on study group assignment
  • Attend nutrition education and Social and Behavior Change Communication (SBCC) sessions if assigned to a voucher group
  • Complete household interviews on food consumption, household expenditures, food security, and nutrition knowledge
  • Participate in dietary assessments and anthropometric measurements for women and children under 5 years of age

Study Overview

Detailed Description

The REVIVE study is a cluster-randomized controlled trial designed to evaluate the effectiveness of revised food voucher interventions combined with nutrition-focused Social and Behavior Change Communication (SBCC) among low-income households in the Philippines. The study will compare three monthly voucher amounts (PhP 3,000, PhP 5,000, and PhP 8,000) with a control group receiving no voucher to assess whether larger voucher values lead to greater improvements in food security, dietary quality, and nutrition-related outcomes.

The intervention includes structured food vouchers with revised allocations emphasizing protein-rich foods, fruits, and vegetables, together with nutrition education sessions delivered by trained local government staff. The study will be implemented across selected urban and rural areas in the Philippines.

Researchers will collect household- and individual-level data through surveys, dietary assessments, and anthropometric measurements to examine the effects of the intervention on household food consumption, nutrition knowledge, food insecurity, dietary quality, and nutritional status among women of reproductive age and children under five years of age. The study will also assess potential spillover effects within participating communities.

Study Type

Interventional

Enrollment (Estimated)

5320

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • District of Columbia
      • Washington D.C., District of Columbia, United States, 20006
        • Recruiting
        • International Food Policy Research Institute
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Households enrolled in the REVIVE study sample drawn from Listahanan 3-eligible low-income households
  • Residency within selected study clusters in the study municipalities
  • Household consent to participate in the study and all survey components
  • Availability of a primary respondent (meal planner or primary food preparer) willing to participate in household interviews
  • For individual dietary assessment components: presence of at least one woman of reproductive age (15-49 years) and/or at least one child under five years of age, where applicable

Exclusion Criteria:

  • Households unwilling or unable to provide informed consent
  • Households not residing within the designated study clusters at the time of baseline data collection
  • Inability to complete core survey modules due to communication barriers or other conditions preventing reliable data collection

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control: No Voucher
Households in this arm do not receive food vouchers during the study period
Experimental: Monthly Food Voucher - PhP 3,000
Households receive a monthly food voucher valued at PhP 3,000, structured with a 10% allocation for carbohydrates and oils, 45% for protein-rich foods, and 45% for fruits and vegetables. Vouchers can be redeemed continuously and are accompanied by six structured nutrition-focused social and behavior change communication (SBCC) sessions delivered by trained local government staff.
Households receive a monthly food voucher valued at PhP 3,000 with a structured allocation of 10% for carbohydrates and oils, 45% for protein-rich foods, and 45% for fruits and vegetables. Vouchers are redeemable continuously throughout the month. The intervention is combined with six structured social and behavior change communication (SBCC) sessions focused on nutrition knowledge, healthy dietary practices, maternal and child nutrition, and WASH behaviors, delivered by trained local government staff.
Experimental: Monthly Food Voucher - PhP 5,000
Households receive a monthly food voucher valued at PhP 5,000, with the same food group allocation (10% carbohydrates and oils, 45% protein, 45% fruits and vegetables) and continuous redemption design. Voucher receipt is combined with six SBCC sessions aimed at improving nutrition knowledge and dietary practices.
Households receive a monthly food voucher valued at PhP 5,000 with the same allocation structure (10% carbohydrates and oils, 45% protein, 45% fruits and vegetables) and continuous redemption design. The voucher is paired with six SBCC sessions covering nutrition education and behavior change topics related to diet quality and household nutrition.
Experimental: Monthly Food Voucher - PhP 8,000
Households receive a monthly food voucher valued at PhP 8,000, structured with 10% allocation for carbohydrates and oils, 45% for protein, and 45% for fruits and vegetables, and redeemed continuously. The intervention is paired with six nutrition-focused SBCC sessions delivered by trained local government personnel to improve dietary behaviors and nutrition knowledge.
Households receive a monthly food voucher valued at PhP 8,000 with the same structured food group allocation and continuous redemption system. The intervention includes six SBCC sessions aimed at improving nutrition knowledge and dietary practices for maternal and child health.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Nutrition Knowledge
Time Frame: Baseline and End of intervention (approximately 24 months)
Composite measure of nutrition knowledge assessed using a structured questionnaire administered to the primary household meal planner. The instrument includes items on food groups, dietary diversity, micronutrient-rich foods, maternal and child feeding practices, and understanding of voucher allocation rules. A total score will be constructed by summing correct responses and standardizing across respondents. Subdomain scores (e.g., dietary diversity knowledge, micronutrient knowledge, child feeding knowledge) will also be analyzed.
Baseline and End of intervention (approximately 24 months)
Individual Nutrient Adequacy
Time Frame: End of intervention (approximately 24 months)
Summary measure of dietary nutrient adequacy among women of reproductive age and children under five years, derived from 24-hour dietary recall data. Probability of adequacy will be estimated for energy, macronutrients, and selected micronutrients (vitamin A, B-complex vitamins, vitamin C, calcium, iron, and zinc). The mean probability of adequacy will be calculated by averaging across 11 micronutrients.
End of intervention (approximately 24 months)
Minimum Dietary Diversity for Women (MDD-W)
Time Frame: End of intervention (approximately 24 months)
Minimum Dietary Diversity for Women (MDD-W), defined as the proportion of women of reproductive age who consume foods from at least 5 of 10 food groups during the previous 24 hours, based on a 24-hour dietary recall.
End of intervention (approximately 24 months)
Global Dietary Quality Score (GDQS)
Time Frame: End of intervention (approximately 24 months)
Global Dietary Quality Score (GDQS), a food-based metric derived from 24-hour dietary recall data that assesses overall dietary quality by accounting for consumption of both healthy and unhealthy food groups. GDQS ranges from 0 to 49, with higher scores indicating better dietary quality and lower risk of nutrient inadequacy and diet-related non-communicable diseases.
End of intervention (approximately 24 months)
Hunger and Food Insecurity Experience Scale
Time Frame: Baseline and End of intervention (approximately 24 months)

Household food insecurity and hunger will be assessed using the Food Insecurity Experience Scale (FIES), an experience-based measure consisting of eight questions about access to adequate food during the previous 4 weeks. The scale captures a range of food insecurity experiences, including worry about obtaining food, reduced dietary quality, reduced food quantity, skipping meals, and going without food.

The raw FIES score ranges from 0 to 8, with higher scores indicating greater severity of food insecurity and hunger. Responses will be used to calculate both continuous FIES scores and categorical classifications of food insecurity severity.

Baseline and End of intervention (approximately 24 months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Household Food Consumption Score (FCS)
Time Frame: Baseline and endline (approximately 24 months after baseline survey)

The Food Consumption Score (FCS) is a composite measure of household dietary diversity, food frequency, and relative nutritional importance of foods consumed. The FCS is calculated using a 7-day recall of household food consumption across standardized food groups. Consumption frequencies are weighted according to the nutritional value of each food group and summed to generate the total score.

The FCS ranges from 0 to 112, with higher scores indicating better household food consumption, greater dietary diversity, and improved food access. Lower scores indicate poorer food consumption patterns and greater vulnerability to food insecurity.

Baseline and endline (approximately 24 months after baseline survey)
Height-for-Age Z-score (HAZ) in Children Under Five Years of Age
Time Frame: End of intervention (approximately 24 months)
Height-for-age z-score (HAZ) among children under five years of age, calculated using the World Health Organization (WHO) Child Growth Standards. HAZ is a standardized measure of linear growth relative to age and sex. HAZ values typically range from approximately -6 to +6, with higher values indicating better growth status. Children with HAZ < -2 standard deviations are classified as stunted.
End of intervention (approximately 24 months)
Weight-for-Age Z-score (WAZ) in Children Under Five Years of Age
Time Frame: End of intervention (approximately 24 months)
Weight-for-age z-score (WAZ) among children under five years of age, calculated using the World Health Organization (WHO) Child Growth Standards. WAZ is a standardized measure of body weight relative to age and sex. WAZ values typically range from approximately -6 to +6, with higher values indicating better nutritional status. Children with WAZ < -2 standard deviations are classified as underweight.
End of intervention (approximately 24 months)
Weight-for-Height Z-score (WHZ) in Children Under Five Years of Age
Time Frame: End of intervention (approximately 24 months)
Weight-for-height z-score (WHZ) among children under five years of age, calculated using the World Health Organization (WHO) Child Growth Standards. WHZ is a standardized measure of body weight relative to height. WHZ values typically range from approximately -5 to +5, with higher values indicating better nutritional status. Children with WHZ < -2 standard deviations are classified as wasted.
End of intervention (approximately 24 months)
Body Mass Index (BMI) Among Women of Reproductive Age
Time Frame: End of intervention (approximately 24 months)
Body mass index (BMI) among women of reproductive age, calculated as weight in kilograms divided by height in meters squared (kg/m²). BMI is a continuous measure of nutritional status. Higher BMI values indicate greater body mass relative to height. Nutritional status categories (underweight, normal weight, overweight, and obesity) will be classified according to World Health Organization (WHO) standard cut-offs and Asian-specific cut-offs
End of intervention (approximately 24 months)
Household Food and Non-food Expenditure
Time Frame: Baseline and End of intervention (approximately 24 months)
Total household food expenditure over a 4-week recall period, including food purchased, produced, received as transfers, and redeemed through food vouchers. Monthly-equivalent household expenditures on non-food categories including health, education, housing, utilities, transport, communication, clothing, durable goods, debt repayment, and other miscellaneous expenditures
Baseline and End of intervention (approximately 24 months)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 29, 2026

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

March 30, 2027

Study Registration Dates

First Submitted

May 18, 2026

First Submitted That Met QC Criteria

June 6, 2026

First Posted (Actual)

June 10, 2026

Study Record Updates

Last Update Posted (Actual)

June 10, 2026

Last Update Submitted That Met QC Criteria

June 6, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified individual participant data (IPD), including household survey data, dietary intake data, anthropometric measurements may be shared after completion of the study. Data sharing will be subject to approval from relevant Philippine government authorities and institutional data governance and ethics requirements. Only fully de-identified datasets will be shared.

IPD Sharing Time Frame

December 2027 and will be available for 2 years

IPD Sharing Access Criteria

Access to de-identified IPD will be granted to qualified researchers upon reasonable request and subject to approval by the study investigators and relevant Philippine government authorities. Data requests must include a clear research proposal and a data use agreement. Data will be shared in a secure format following completion of primary analyses and publication of main study findings.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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