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Acceptability of Soy Milk as a Calcium-Rich Beverage in School Children in New York City Public Schools

NYC Public Schools is testing offering soy milk alongside dairy milk on the lunch line for all students during the month of May at select school sites to understand:

  • Whether students choose and drink soy milk
  • Whether offering soy milk can reduce milk waste
  • The potential environmental, nutrition, and cost impacts

Studieoversikt

Detaljert beskrivelse

Acceptability of Soy Milk as a Calcium-Rich Beverage in School Children in New York City Public Schools.

The study intervention proposal:

In the spring and fall of 2026, the investigators aim to test the acceptability of soy milk over a four-week period of time in 11 New York City Public Schools. Leading up to the intervention, the investigators will take baseline measurements of cow's milk, both sales and amount of beverage consumed. During the 4-week intervention, there will be taste tests at each school. At the end of the intervention, the investigators will measure consumption of both cow's milk and soy milk. Students will be offered a sticker for tasting the soy milk and posters and other marketing materials will be utilized in schools. No information, identifiable or otherwise will be collected from the students. In addition to student acceptability, the investigators aim to determine whether calcium was increased as a result of bringing soy milk into the lunch line. This is a replication of a study our team published April 2006 in the Journal of the AMERICAN DIETETIC ASSOCIATION. In coordination with the New York City Office of Food and Nutrition Services and non-profit partners, the investigators will conduct a pilot with 11 schools to see how many students take soy milk, and to report on associated food waste. With the results, this will inform the school system with information about expanding access to soy milk and the investigators aim to publish the results to inform other food service staff across the United States about the acceptability of soy milk in school lunch programs.

The pilot will include a variety of elementary, middle, and high schools that opt into the program and they will be grades K-12 and ages 5-18. The New York City Office of Food and Nutrition Services team will invite individual schools to participate and for those who opt in, a virtual and in person training will be provided for both the administrators and food service teams at all schools. The study team will be onsite to administer the consumption measurements and the taste tests.

School administrators and food service staff will be provided an informational training that will include a Power Point presentation describing the pilot program, detailing the taste test, as well as safety measures for those with allergies. Principals will have a notification letter for parents as well as a Frequently Asked Question document about the pilot and soymilk. Schools will also be provided promotional fliers and stickers to share with students upon their discretion.

To assess and/or address any soy milk allergies during the taste testing:

Students often submit an allergy/504 plan or a dietary accommodation request if they have an allergy, and therefore the investigators will be including both the school nurse (if applicable) and cafeteria manager in the pilot training so the investigators can ensure all students who have a documented allergy are notified they cannot partake in the taste test. the investigators will also provide training on avoiding students with allergies in our training. Nurses will be invited to the training and the investigators will ensure that there is uniform communication across all channels needed prior to taste test.

Studietype

Observasjonsmessig

Registrering (Antatt)

2500

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

  • Navn: Zeeshan Ali, PhD
  • Telefonnummer: 202-527-7302
  • E-post: zali@PCRM.org

Studer Kontakt Backup

Studiesteder

    • New York
      • Elmhurst, New York, Forente stater, 11373
      • Flushing, New York, Forente stater, 11355
      • New York, New York, Forente stater, 10036
      • Staten Island, New York, Forente stater, 10301
      • The Bronx, New York, Forente stater, 10454
      • The Bronx, New York, Forente stater, 10472
        • Rekruttering
        • Vertex Academy
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen

Tar imot friske frivillige

Ja

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Elementary, middle, and high school children, grades K-12 and ages 5-18, who opt into the program

Beskrivelse

Inclusion Criteria:

  • Students at the 11 participating New York City Public Schools
  • Students opting to join the pilot program and broader study

Exclusion Criteria:

  • Students opting out of the study
  • Students with soy allergies

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Elementary, Middle and High School Kids
The pilot will include a variety of elementary, middle, and high schools that opt into the program and they will be grades K-12 and ages 5-18.
In the spring and fall of 2026, the investigators aim to test the acceptability of soy milk over a four-week period of time in 11 New York City Public Schools. Leading up to the intervention, the investigators will take baseline measurements of cow's milk, both sales and amount of beverage consumed. During the 4-week intervention, there will be taste tests at each school and measurements of consumption of both cow's milk and soy milk. At the end of the intervention, the investigators will measure consumption of both cow's milk and soy milk.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Acceptability of Soy milk
Tidsramme: 4 weeks
Number of students who choose and drink soy milk or cow's milk. The quantity of soy milk and cow's milk consumed.
4 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Measurement of how much cow's milk and soy milk was consumed and how much was sold during the pilot study
Tidsramme: 4 weeks
The investigators will measure how much each milk was consumed and how much each milk was wasted.
4 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Jill Eckart, Physicians Committee for Responsible Medicine

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

7. mai 2026

Primær fullføring (Antatt)

1. mai 2027

Studiet fullført (Antatt)

1. desember 2027

Datoer for studieregistrering

Først innsendt

12. mai 2026

Først innsendt som oppfylte QC-kriteriene

12. mai 2026

Først lagt ut (Faktiske)

19. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

26. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

21. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • PCRMSM2026

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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