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CompletedNCT02202733Updated Jul 14, 2015

Skill-based Cooking Intervention to Reduce Eating Out

An interventional study of Cooking in Obesity, sponsored by Children's Hospital Medical Center, Cincinnati. Completed at 1 site in United States. Open to participants aged 3 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-07-14.

Sponsored by Children's Hospital Medical Center, Cincinnati · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
33
Allocation
Not applicable
Ages
3 Years and older
Sex
All
01

Study summary

The primary goal of the study is to use an iterative process to develop and refine a skill-based cooking intervention to decrease the consumption of energy from foods prepared away from home for evening meals, decrease energy intake, and promote a healthy weight in parents and children aged 3-10 years.

Read the detailed description

Phase I. Conduct 2-4 focus groups with 6-10 caretaker, who report eating foods prepared away from home ≥3 times per week, per group to gain insight into current eating behaviors of foods prepared away from home, current perceptions about a home prepared evening meal, and barriers to preparing evening meals at home. Information gathered during Phase I will be used to inform intervention development in Phase II.

Phase II. Develop, refine, and manualize a skill-based cooking intervention for overweight/obese caretakers of a child aged 3-10 years. The aim of Phase II is to test the feasibility of a skill-based cooking intervention to reduce the consumption of foods prepared away from home for the evening meal (e.g., pre-prepared frozen foods, restaurant foods, fast food, take-out), energy intake from evening meals, and promote a healthy weight in parents and children. Information collected during Phase I will inform the development of the skill-based cooking intervention. Once developed, the intervention will be refined with 6 primary caretakers of a child, who meet criteria for being overweight/obese during a testing phase. Conducting the intervention with at least six families will provide the opportunity for further refinement of intervention procedures. The results will be important to demonstrate feasibility for a future pilot randomized controlled trial that will test the impact of a skill-based cooking intervention compared to a standard cooking demonstration where recipes are simply provided to families.

02

Conditions studied

  • Obesity

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Keywords

  • cooking skills
  • eating out
  • foods prepared away from home
03

In context

Obesity

6,570 studies on the registry are indexed under Obesity; 1,718 are open to participants now.

This study's enrollment of 33 is below the median of 77 across 5,084 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Children's Hospital Medical Center, Cincinnati is the lead sponsor of 673 studies on the registry; 134 are open to participants now.

Of its 56 completed or terminated interventional studies of FDA-regulated products, 31 (55%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria (Phase I):

  • be ≥18 years of age
  • have a child between the ages of 3 and 10 years-old
  • report being the primary caretaker and have the primary feeding responsibility of the child for dinner/supper
  • able to read, speak, and understand English
  • have transportation to the Medical Center
  • report their family including the child eats pre-prepared frozen food, restaurant food, fast food, or take-out for dinner ≥3 times per week
  • has a working telephone number
  • is able to attend the scheduled date and time of a focus group.

Inclusion Criteria (Phase II):

  • caretaker is ≥18 years of age
  • caretaker is overweight or obese (BMI≥25)
  • has a child between the ages of 3 and 10 years-old
  • report being the primary caretaker and have the primary feeding responsibility of the child for dinner/supper
  • caretaker is able to read, speak, and understand English
  • has transportation to the medical center and the instructional kitchen
  • does not plan to move out of the area before June 2015
  • reports their family including the child eats convenience food, restaurant food, fast food, or take-out for dinner ≥3 times per week
  • reports access to a kitchen
  • able to attend the scheduled date and time of the sessions.

Exclusion Criteria (Phase II):

  • the caretaker or child is currently participating in a weight loss program and/or taking weight loss medication
  • have a medical condition known to promote growth (e.g., Prader-Willi syndrome, Cushing's syndrome) or had gastric bypass surgery.
05

Study design

Phase
Not applicable
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
33 participants (actual)

Study arms

  • Other
    Cooking

    A skill-based cooking intervention for caretakers of an overweight/obese child aged 3-10 years.

    Other: Cooking

Interventions

  • OtherCooking

    The aim is to test the feasibility of a skill-based cooking intervention to reduce the consumption of foods prepared away from home for the evening meal (e.g., pre-prepared frozen foods, restaurant foods, fast food, take-out), energy intake from evening meals, and parent/child weight status.

06

What researchers measure

Primary outcomes

  1. Dietary Intake (Phase II only)

    Caregivers will be asked to complete a 7-day dietary record of what they and their child eat at the evening meal. For each evening meal, the caretaker will be asked to describe the meal type (fast food, restaurant, pre-prepared frozen meal, or home prepared); the specific foods and drinks consumed, and the amount consumed by the child. Data from dietary records will be input into Nutrition Data System for Research (NDSR) software and analyzed for energy intake, percent energy from fat, and food groups (fruits, vegetables, grains, proteins, dairy) from the evening meal. Foods prepared away from home will be classified based on caretaker indication of fast food, restaurant, pre-prepared frozen meal, or home prepared on the dietary record.

    Time frame: 0 and 10 weeks

Secondary outcomes

  1. Caretaker Attitudes and Confidence

    Caretakers will report ease of providing foods prepared away from home (i.e., pre-prepared frozen meals, restaurant food, fast food, take-out) for an evening meal, ease of providing a home prepared evening meal, and their confidence with meal preparation using a 100-mm visual analog scale (VAS). Further caretakers will rate their ability, enjoyment of cooking and desire to cook on a 100-mm VAS.

    Time frame: 0 and 10 weeks

  2. Food Costs

    Caretakers will be provided with four visual images with each image showing one adult evening meal and two child evening meals. Caretaker will record the total cost of the meals shown in each image.

    Time frame: 0 and 10 weeks

  3. Portions

    Caretakers will be provided with visual images of foods in different portion amounts and asked to identify which image best represents the amount their child would be served for dinner. Caretakers will also identify the images that best represent the amount they would serve themselves for dinner.

    Time frame: 0 and 10 weeks

  4. Dinner Choices

    Caretakers will complete a 10-question, open-ended questionnaire that solicits information related to choices of foods prepared away from home and foods prepared at home.

    Time frame: 0 and 10 weeks

  5. Anthropometrics

    Height and weight will be measured using standard procedures.

    Time frame: 0 adn 10 weeks

07

Study locations

1 site
  • Cincinnati Children's Hospital Medical Center
    Cincinnati, Ohio 45229, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02202733
Responsible party
Sponsor
First posted
Jul 29, 2014
Start date
Apr 2014
Primary completion
Sep 2014
Completion
Sep 2014
Last update
Jul 14, 2015

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2015. You cannot join it, but the record below documents what was studied.

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