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

6 juin 2026 mis à jour par: 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

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Estimé)

5320

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

    • District of Columbia
      • Washington D.C., District of Columbia, États-Unis, 20006
        • Recrutement
        • International Food Policy Research Institute
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La 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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Aucune intervention: Control: No Voucher
Households in this arm do not receive food vouchers during the study period
Expérimental: 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.
Expérimental: 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.
Expérimental: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Nutrition Knowledge
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Household Food Consumption Score (FCS)
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

29 avril 2026

Achèvement primaire (Estimé)

30 juin 2026

Achèvement de l'étude (Estimé)

30 mars 2027

Dates d'inscription aux études

Première soumission

18 mai 2026

Première soumission répondant aux critères de contrôle qualité

6 juin 2026

Première publication (Réel)

10 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

10 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

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.

Délai de partage IPD

December 2027 and will be available for 2 years

Critères d'accès au partage IPD

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.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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