- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05907278
Advanced Cooking Education Feasibility Study
The Advanced Cooking Education (ACE) 4-H After School Club: A Feasibility Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
Ithaca, New York, United States, 14853
- Cornell University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 7th and 8th grade students attending Title I funded schools in New York City
- Caregivers of 7th and 8th grade students attending Title I funded schools in New York City
Exclusion Criteria:
- Do not speak/understand English
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
The ACE Program is a culturally inclusive, 4-H after school club where youth meet once a week for 12 weeks virtually.
They also receive groceries to make a meal 1 day a week.
|
Participants attend the ACE Program for 12 weeks after school. On one assigned day of the week, participants attend ACE virtually. The session will begin with mindfulness exercises (15 minutes), professional development session (50 minutes), nutrition education lesson (20 minutes), and reflection period to talk about their experience in cooking lessons (25 minutes). On any day during the week, the students will make a dish using groceries they received (1 hour). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in diet quality, measured by the Healthy Eating Index Scores
Time Frame: Baseline, 12 weeks [endpoint]
|
Scores are calculated from three 24-hour diet records, range from 0-100.
Higher score reflects higher alignment between one's diet and recommendations from Dietary Guidelines for Americans
|
Baseline, 12 weeks [endpoint]
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in body mass index
Time Frame: Baseline, 12 weeks [endpoint]
|
Height will be measured using stadiometer to nearest decimal point in cm.
Weight measured using scale to nearest decimal in kg.
Body mass index calculated using kg/m^2.
|
Baseline, 12 weeks [endpoint]
|
|
Change in body fat percentage
Time Frame: Baseline, 12 weeks [endpoint]
|
Measured using a scale to nearest decimal
|
Baseline, 12 weeks [endpoint]
|
|
Change in waist circumference
Time Frame: Baseline, 12 weeks [endpoint]
|
Measured using a waist circumference tape to the nearest decimal in cm.
|
Baseline, 12 weeks [endpoint]
|
|
Change in dermal carotenoids level
Time Frame: Baseline, 12 weeks [endpoint]
|
Measured using the Veggie Meter device, range from 0-800.
Higher score acts as proxy for increased fruits and vegetables consumption.
|
Baseline, 12 weeks [endpoint]
|
|
Change in household food security
Time Frame: Baseline, 12 weeks [endpoint]
|
Short form food security survey module by the USDA
|
Baseline, 12 weeks [endpoint]
|
|
Change in child food security
Time Frame: Baseline, 12 weeks [endpoint]
|
Child version of food security survey module by the USDA
|
Baseline, 12 weeks [endpoint]
|
|
Change in culinary skills
Time Frame: Baseline, 12 weeks [endpoint]
|
iCook program youth culinary skill survey with 5-point likert scale questions with higher scores indicate higher skill level (better outcome).
Min=7, Max=35
|
Baseline, 12 weeks [endpoint]
|
|
Change in culinary attitudes
Time Frame: Baseline, 12 weeks [endpoint]
|
Cooking with kids survey with 5-point likert scale questions with higher scores indicate more positive attitude (better outcome).
Min=6, Max=30
|
Baseline, 12 weeks [endpoint]
|
|
Change in culinary self-efficacy
Time Frame: Baseline, 12 weeks [endpoint]
|
iCook program youth culinary self-efficacy survey with 5-point likert scale questions with higher scores indicate higher self-efficacy (better outcome).
Min=6, Max=30.
|
Baseline, 12 weeks [endpoint]
|
|
Change in perceived stress
Time Frame: Baseline, 12 weeks [endpoint]
|
Used the Cohen perceived stress scale.
Higher scores mean increased stress (worse outcome).
Min=0, Max=40
|
Baseline, 12 weeks [endpoint]
|
|
Change in food neophobia
Time Frame: Baseline, 12 weeks [endpoint]
|
FNTT10 survey with 5-point likert scale questions, higher scores mean less neophobia (better outcome).
Min=10, Max=50.
|
Baseline, 12 weeks [endpoint]
|
|
Change in sense of purpose
Time Frame: Baseline, 12 weeks [endpoint]
|
Used the Clarement Purpose Scale survey questions, higher scores mean higher sense of purpose (better outcome).
Min=12, Max=60
|
Baseline, 12 weeks [endpoint]
|
|
Change in social and emotional competency
Time Frame: Baseline, 12 weeks [endpoint]
|
Used the SEC survey by CASEL, higher scores mean higher competence (better outcome).
Min=17, Max= 68
|
Baseline, 12 weeks [endpoint]
|
|
Change in family mealtime beliefs
Time Frame: Baseline, 12 weeks [endpoint]
|
Calculated based on the Fulkerson family mealtime survey.
A total of 9 questions that are scored independently.
Each: Min=1, Max=4.
Higher scores indicate better family mealtime practices (better outcome).
|
Baseline, 12 weeks [endpoint]
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Tashara M Leak, PhD RD, Cornell University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 0009007
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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