Advanced Cooking Education Pilot Study

Sponsor
Cornell University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05926141
Collaborator
United States Department of Agriculture (USDA) (U.S. Fed)
22
1
2
14.1
1.6

Study Details

Study Description

Brief Summary

The aim of this study is to assess the impact of an in-person multi-component Advanced Cooking Education (ACE) 4-H after school program. The ACE Program consists of mindfulness, nutrition education, cooking labs, and professional development activities.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: ACE intervention
N/A

Detailed Description

The ACE program is conducted with 7th and 8th grade students attending New York City (NYC) Title I middle schools. Participants attend weekly sessions (2hour) after school to participate in mindfulness, nutrition lessons, and professional development activities. On another day in the week, students participate in cooking labs at their own time at their homes. The investigators hypothesize that after the program, adolescents' diet quality, cooking-related skills, stress levels will be improved compared to prior of the program.

Study Design

Study Type:
Interventional
Actual Enrollment :
22 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
All participants enter a control phase for 12 weeks where they receive no intervention. After 12 weeks, participants receive the ACE intervention.All participants enter a control phase for 12 weeks where they receive no intervention. After 12 weeks, participants receive the ACE intervention.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Advanced Cooking Education (ACE) 4-H After School Club Pilot Study
Actual Study Start Date :
Sep 28, 2022
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control phase

After the first data collection session, participants spend 12 weeks and enter a "control phase" where they receive no intervention. At the end of the 12 weeks, participants will attend another data collection session.

Experimental: ACE intervention

The ACE Program is a culturally inclusive, 4-H after school club where youth meet once a week for 12 weeks after school in person. They also receive groceries to make a meal 1 day a week.

Behavioral: ACE intervention
Participants attend the ACE Program for 12 weeks after school. On one assigned day of the week, participants attend ACE in person after school. The session begins 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).

Outcome Measures

Primary Outcome Measures

  1. Difference in change in diet quality between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Healthy Index Eating 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

Secondary Outcome Measures

  1. Difference in change in body mass index between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Height will be measured using stadiometer to nearest decimal point in cm. Weight is measured using scale to nearest decimal in kg. Body mass index calculated using kg/m^2.

  2. Difference in change in body fat percentage between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Measured using a scale to nearest decimal

  3. Difference in change in waist circumference between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Measured using a waist circumference tape to the nearest decimal in cm

  4. Difference in change in dermal carotenoids level between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Measured using the Veggie Meter device, range from 0-800. Higher score acts as proxy for increased fruits and vegetables consumption

  5. Difference in change in household food security between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Short form food security survey module by the USDA

  6. Difference in change in child food security between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Child version of food security survey module by the USDA

  7. Difference in change in culinary skills between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    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

  8. Difference in change in culinary self-efficacy between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    iCook program youth culinary self-efficacy survey with 5-point likert scale questions with higher scores indicate higher skill level (better outcome). Min=6, Max=30

  9. Difference in change in culinary attitudes between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Cooking with kids survey with 5-point likert scale questions with higher scores indicate more positive attitude (better outcome). Min=6, Max=30

  10. Difference in change in perceived stress between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Used the Cohen perceived stress scale. Higher scores mean increased stress (worse outcome). Min=0, Max=40

  11. Difference in change in food neophobia between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    FNTT10 survey with 5-point likert scale questions, higher scores mean less neophobia (better outcome). Min=10, Max=50.

  12. Difference in change in sense of purpose between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Used the Clarement Purpose Scale survey questions, higher scores mean higher sense of purpose (better outcome). Min=12, Max=60

  13. Difference in change in social and emotional competency between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    Used the SEC survey by CASEL, higher scores mean higher competence (better outcome). Min=17, Max= 68

  14. Difference in change in family mealtime beliefs between intervention phase (12-24wk) and control phase (0wk-12wk) [0 weeks, 12 weeks, 24 weeks, 48 weeks]

    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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 7th and 8th grade students attending Title I funded schools in New York City

  • Caregivers of the 7th and 8th grade students attending Title I funded schools in New York City

Exclusion Criteria:
  • Do not speak/understand English

  • Those who have previously participated in the Virtual ACE program (Feasibility Study)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cornell University Ithaca New York United States 14853

Sponsors and Collaborators

  • Cornell University
  • United States Department of Agriculture (USDA)

Investigators

  • Principal Investigator: Tashara M Leak, PhD RD, Cornell University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cornell University
ClinicalTrials.gov Identifier:
NCT05926141
Other Study ID Numbers:
  • 0145840
First Posted:
Jul 3, 2023
Last Update Posted:
Jul 3, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Cornell University

Study Results

No Results Posted as of Jul 3, 2023