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Recruiting NCT06362837

NCT06362837 Evaluation of REACTS-IN, an Intervention to Improve Nutrition, Hygiene, and Sexual and Reproductive Health Services

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Clinical Trial Summary
NCT ID NCT06362837
Status Recruiting
Phase
Sponsor McGill University
Condition Stunting
Study Type INTERVENTIONAL
Enrollment 13,500 participants
Start Date 2024-09-01
Primary Completion 2029-06-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Education intervention on nutrition, gender equity, WASH, sexual and reproductive health rightsschool-based iron-folic acid supplement programHealth service training on equitable access to nutrition, health, and sexual and reproductive services

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 13,500 participants in total. It began in 2024-09-01 with a primary completion date of 2029-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is an independent evaluation of World VIsion's 7-year quasi-experimental intervention to improve nutrition, nutrition-related rights and gender equality for women, adolescent girls, and children under five years of age in rural Bangladesh, Kenya, and Tanzania. The evaluation will collect baseline, midline, and end-line data from intervention communities, schools, and health facilities. Only baseline and endline will be collected on the comparison communities. The evaluation objectives are to test if the intervention improved indicators for (i) child anthropometry, (ii) maternal and child dietary practices, (iii) women's empowerment, and (iv) equitable health service access for nutrition and sexual and reproductive needs. The evaluation analysis will take into account gender differences in the indicators.

Eligibility Criteria

Inclusion Criteria: (i)Women: * 15-49 y of age * biological mother of child in the home who is 0-5.9, 6-23.9, or 24-59.9 months * has lived in the community for at 12 months (ii) Husbands/partners: * no age limit * lives in the home with index woman * has lived in community for at least 12 months (iii) Adolescents: * 10-19 years * male or female * has been in target school for at least 6 months * lives in the target community (iv) Children: * 0-5.9, 6-23.9, or 24-59.9 months Exclusion Criteria: (i) Children: * no limitation on normal diet or growth (birth defects, illnesses)

Contact & Investigator

Central Contact

Grace S Marquis, PhD

✉ grace.marquis@mcgill.ca

📞 1-514-398-7839

Principal Investigator

Grace S Marquis, PhD

PRINCIPAL INVESTIGATOR

McGill University

Frequently Asked Questions

Who can join the NCT06362837 clinical trial?

This trial is open to participants of all sexes, studying Stunting. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06362837 currently recruiting?

Yes, NCT06362837 is actively recruiting participants. Contact the research team at grace.marquis@mcgill.ca for enrollment information.

Where is the NCT06362837 trial being conducted?

This trial is being conducted at Dhaka, Bangladesh, Nairobi, Kenya, Ifakara, Tanzania.

Who is sponsoring the NCT06362837 clinical trial?

NCT06362837 is sponsored by McGill University. The principal investigator is Grace S Marquis, PhD at McGill University. The trial plans to enroll 13,500 participants.

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