- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07609368
Teaching Kitchens Intervention for Older Adults in a Senior Center in New England
19. maj 2026 opdateret af: Tufts University
A Pilot Teaching Kitchens Intervention Protocol to Improve the Dietary Quality of Congregate Meals for Older Adults
This study will evaluate a culinary nutrition intervention designed to improve the quality of meals served to older adults participating in a senior center.
Many meals currently provided in these settings do not meet recommended dietary guidelines, which negatively impact health outcomes among older adults.
In this pilot study, participants will receive improved lunch meals that are designed to be more nutritious, culturally appropriate, and acceptable, along with nutrition education sessions over a 6-month period.
This intervention will also include training for food service staff to support implementation of the improved meals.
The study will assess changes in dietary quality, physical health measures, and social and behavioral outcomes among participants at baseline, 3 months, and 6 months.
Findings from this study will help determine the feasibility and effectiveness of this approach and inform future efforts to improve nutrition and health outcomes in Congregate Meal Program for older adults.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Detaljeret beskrivelse
Congregate meal programs within senior centers serve a large population of older adults in the United States, yet many meals provided in these settings do not meet recommended dietary guidelines particularly for whole grains, micronutrients, sodium, and saturated fat.
Poor dietary quality in this population may contribute to increased risk of chronic diseases, reduced physical function, and lower overall well-being.
This study is a Phase III pilot feasibility study designed to evaluate a culinary nutrition intervention implemented in a senior meal center serving older adults.
The intervention is based on a Teaching Kitchens model and includes three core components: (1) development and implementation of a nutritionally improved lunch menu, (2) training of food service staff to prepare healthier and culturally appropriate meals, and (3) delivery of nutrition education sessions to meal recipients.
The intervention will be conducted over a 6-month period.
Participants will receive reformulated lunch meals designed to improve dietary quality, alongside structured nutrition education sessions aimed at increasing nutritional literacy, supporting healthy food choices, and promoting engagement in the meal program.
The effectiveness of the intervention will be evaluated by measuring changes in dietary quality, physical health indicators, and psychosocial outcomes at baseline, 3 months, and 6 months.
Outcomes will include dietary intake, anthropometric measures (e.g., body weight, hip-to-waist circumference, height), blood pressure, food security, and measures of social engagement and well-being.
This study aims to assess the feasibility and preliminary effectiveness of a scalable culinary nutrition intervention tailored to older adults in Congregate meal settings.
Findings from this pilot study will inform the development of larger-scale interventions and may contribute to improving nutrition and health outcomes for older adults in similar programs.
Undersøgelsestype
Observationel
Tilmelding (Anslået)
30
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Andres V Ardisson Korat, ScD
- Telefonnummer: 617-556-3386
- E-mail: andres.ardisson_korat@tufts.edu
Undersøgelse Kontakt Backup
- Navn: Meghan Hendricksen, Ph.D
- Telefonnummer: 617-556-3384
- E-mail: meghan.hendricksen@tufts.edu
Studiesteder
-
-
Connecticut
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Glastonbury, Connecticut, Forenede Stater, 06033
- Glastonbury Senior Center
-
Kontakt:
- Ronda Guberman, Senior Center Supervisor
- Telefonnummer: 860-652-7646
- E-mail: ronda.guberman@glastonbury-ct.gov
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
The participants for this study are senior center members either of the current lunch program or other programming events at "The Senior Center" in Glastonbury, Connecticut.
Beskrivelse
Inclusion Criteria:
- Age 50 years or older
- Regularly visits the Senior Center either for lunch meals or other center-based programming
- Willing and able to participate in a 6-month intervention, which includes consistent involvement in the lunch program
- Willing and able to participate in multiple focus group discussions centered around meal preferences, health perceptions, and dietary habits (full study participation is 7 months)
- Capable of providing informed consent and completing an eligibility screening
Exclusion Criteria:
- History of moderate to severe neurological condition(s) that may impact cognitive ability (e.g., dementia, major stroke)
- Known severe food allergies that may interfere with participation. (with study MD approval, participants with mild allergies or intolerances may be included and notified not to consume any known allergens)
- Recent changes in health status that affect the ability to assess foods (e.g., altered appetite, smell, vision, hearing, and/or taste)
- Any disorder, unwillingness, or inability, not covered by any of the other exclusion criteria, which, in either the investigator's or study MD's opinion, might jeopardize the subject's compliance with the protocol. This includes impaired vision requiring assistance or aid from another person, impaired smell, or impaired taste perception. Given the number of written surveys and visual support materials, the study would place a large burden on participation for individuals with visual impairment requiring assistance.
- Individuals who have a cognitive, sensory, or physical impairment that prevents them from understanding the consent information or completing the required consent documentation will be excluded from participation.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
|---|
|
Senior Center Meal Recipients
Adults aged 50+ who regularly attend The Senior Center in Glastonbury, CT and participate in the 6-month culinary nutrition intervention, including redesigned lunch meals, nutrition education sessions, focus groups, and dietary/health assessments.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Mean change from baseline to 6 months in dietary quality among meal recipients
Tidsramme: Baseline to 6 months
|
The mean change from baseline to 6 months in dietary quality among meal recipients will be measured using the healthy eating index (HEI) and individual components of the HEI.
|
Baseline to 6 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Satisfaction in meal program from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The satisfaction in meal program will be measured using the meal program satisfaction questionnaire from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean meal consumption scores from baseline to 6 months
Tidsramme: Weeks 3 and 7 of meal implementation
|
The mean meal consumption scores will be measured through visual assessment of food discarded during weeks 3 and 7 using the official plate waste analysis guide.
|
Weeks 3 and 7 of meal implementation
|
|
Mean change in nutrition literacy from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in nutrition literacy will be assessed using a nutritional literacy survey for older adults from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean change in blood pressure from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in blood pressure (systolic/diastolic) will be assessed using an automated sphygmomanometer.
|
Baseline to 6 months
|
|
Mean change in body weight from baseline to 6 months
Tidsramme: baseline to 6 months
|
The mean change in body weight will be assessed using a digital scale from baseline to 6 months.
|
baseline to 6 months
|
|
Mean change in waist circumference from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in waist circumference using a tape measure will be assessed from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean change in hip circumference from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in hip circumference using a tape measure will be assessed from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean change in waist-to-hip circumference ratio from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in waist-to-hip circumference ratio will be mathematically calculated from the hip and waist measurements.
|
Baseline to 6 months
|
|
Mean change in height from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in height will be assessed using a stadiometer from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean change in body mass index (BMI) from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in body mass index will be mathematically calculated from the body weight and height measurements from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean change in Food and Nutrition Insecurity from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in food and nutrition insecurity will be measured through validated questionnaires (e.g., US Household Food Security Survey Module) from baseline to 6 months.
|
Baseline to 6 months
|
|
Mean Change in Loneliness and Socialization Measures from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in loneliness and socialization measures using validated questionnaires (e.g., Socialization questionnaire) from baseline to 6 months.
|
Baseline to 6 months
|
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Mean change in frequency of meal participation and participation in other activities at the Senior Center from baseline to 6 months
Tidsramme: Baseline to 6 months
|
The mean change in frequency of meal participation and participation in other activities at the Senior Center will be assessed using the current Senior Center's attendance log.
|
Baseline to 6 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Andres V Ardisson Korat, ScD, Tuft's University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. juli 2026
Primær færdiggørelse (Anslået)
1. marts 2027
Studieafslutning (Anslået)
1. juni 2027
Datoer for studieregistrering
Først indsendt
19. maj 2026
Først indsendt, der opfyldte QC-kriterier
19. maj 2026
Først opslået (Faktiske)
27. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
27. maj 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. maj 2026
Sidst verificeret
1. maj 2026
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- STUDY00007007
- 58-8050-3-003 (Andet bevillings-/finansieringsnummer: USDA Cooperative Agreement)
- PT0445 (Andet bevillings-/finansieringsnummer: Danone Institute of North America)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
Participant privacy given the small sample size (n=30)
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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