CClinicalTrials.gg
CompletedNCT01710423Updated Feb 5, 2015

Peer-mentored Cooking Classes for Parents of Toddlers: Do Families Cook More and Eat Healthier After the Intervention?

An interventional study of Peer mentoring intervention ('Cooking with Friends') in Obesity, sponsored by Children's Hospital of Philadelphia. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2015-02-05.

Sponsored by Children's Hospital of Philadelphia · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
47
Allocation
Randomized
Sex
All
01

Study summary

This study aims to test the effectiveness of a community-located, peer mentored intervention to improve home food preparation practices in families with young children.

Read the detailed description

Barriers to healthy eating and active living are at the heart of the obesity epidemic. This study focuses on a key factor underlying healthy eating: home food preparation. Preparing food at home entails a sequence of steps from obtaining food, to planning and cooking or preparing meals, to finally serving and eating the meal. Many strategies to curb obesity in children focus on eliminating processed and fast food from the diet, as well as improving access to fresh produce and other healthy ingredients. A collective ability to regularly and reliably prepare healthy food at home is implicit in these and other prevention strategies. Little research, however, has grappled with the phenomenon that there has been a generational loss of home food preparation ability over the past few decades. What is urgently needed is to design effective, enticing, and scalable interventions to improve home food preparation practices across diverse groups.

This study aims to test the effectiveness of a community-located, peer mentored intervention to improve home food preparation practices in families with young children. The investigators will partner with Children's Hospital of Philadelphia Early Head Start, a community-based organization serving families with children ages 0 to 3 years in West Philadelphia, aiming specifically to:

  1. Use the principles of Community Based Participatory Research (CBPR) to design, evaluate and disseminate a peer mentored intervention aimed at improving home food preparation practices among families with young children.
  2. Conduct a randomized controlled trial with a delayed entry control group to test the effect of the intervention on three outcomes: home food preparation practices, healthfulness of the diet, and cooking-related self-efficacy.

The investigators hypothesize that families participating in this intervention will demonstrate improvement in parental self-efficacy related to cooking, home food preparation practices, and the healthfulness of parents' and toddlers' diets post-intervention, compared to families who do not participate in the intervention.

02

Conditions studied

  • Obesity

Browse trials for

Keywords

  • Obesity
  • Nutrition
  • Home Food Preparation
  • Peer Mentoring
  • Early Head Start
  • Cooking
  • Diet
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,692 are open to participants now.

This study's enrollment of 47 is below the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

Children's Hospital of Philadelphia is the lead sponsor of 480 studies on the registry; 85 are open to participants now.

Of its 28 completed or terminated interventional studies of FDA-regulated products, 22 (79%) have results posted.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Mentee Inclusion Criteria:

  1. Eligible mentees will be caregivers of 0-3 year old children who are enrolled in Early Head Start at The Children's Hospital of Philadelphia (CHOP EHS) at the time of recruitment.
  2. Caregiver enrollment in CHOP EHS requires the following:

    1. Children are 0-3 years old (Expectant mothers are also eligible to enroll)
    2. The family has an income at or below federal poverty level
    3. The family lives in West Philadelphia, within the geographic area served by CHOP EHS.
  3. Caregiver is able to give informed consent.

Mentor Inclusion Criteria:

  1. Eligible peer mentors should meet the inclusion criteria set for above for mentees.
  2. The study team, in conjunction with EHS staff, will decide which participants will be invited to be peer mentors, based on attributes including interest, leadership ability, and home food preparation skills.

Children Inclusion Criteria:

  1. 0-3 year old children of mentee caregivers enrolled in the study
  2. If a mentee caregiver has more than one child currently enrolled in CHOP EHS, then all their eligible children will be enrolled in the study.
  3. If there are expectant mothers who are enrolled as mentees, their children will be enrolled in the study upon delivery.

Exclusion Criteria:

  1. Caregivers and children not meeting the inclusion criteria above.
  2. Subjects who, in the opinion of the Investigator, may be unable to participate in the study schedules or procedures.
  3. Children of peer mentors will not be eligible for this study.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
47 participants (actual)

Study arms

  • Experimental
    Immediate Intervention

    Peer mentoring intervention ('Cooking with Friends')

    Behavioral: Peer mentoring intervention ('Cooking with Friends')

  • No intervention
    Delayed Entry Control

Interventions

  • BehavioralPeer mentoring intervention ('Cooking with Friends')

    'Cooking with Friends' is a community-located, peer mentoring intervention aimed at improving home food preparation practices in families with young children. The intervention was developed in an iterative, community-based research approach, and will be conducted in partnership with Early Head Start (EHS) at The Children's Hospital of Philadelphia. Cooking with Friends builds on existing monthly cooking classes at EHS that have proven popular with EHS families. Through 5 weekly classes, this intervention will explore topics of how to prepare healthy foods at home. The peer mentoring component is a novel innovation to this intervention. The intervention pairs peer mentors to individual mentees in a community setting, to effect behavioral change among caregivers of young children.

06

What researchers measure

Primary outcomes

  1. Food Frequency Questionnaire

    The primary outcome will be the change in healthfulness of the diet as measured by food frequency questionnaires for participants through the course of the study. Study staff will meet with each participant and ask them to answer questions about the frequency of their food and beverage consumption over the course of a 12 month period. The results will be analyzed for consumption of specific food-groups (fruits, vegetables, whole grains, dairy, etc.). The primary endpoint is the difference in the healthfulness of the diet between the immediate intervention group and the control group at week 23.

    Time frame: 23 weeks from Baseline

Secondary outcomes

  1. Cooking-related self-efficacy

    Self-efficacy related to cooking will be measured using a 25-item instrument. We will assess to assess the difference between the immediate intervention group and the control group at week 23.

    Time frame: 23 weeks from Baseline

  2. Home food preparation practices

    Home food preparation practices will be measured using questions from the National Health and Nutrition Examination Survey. We will measure the difference in home food preparation practices between the immediate intervention group and the control group at week 23.

    Time frame: 23 weeks from Baseline

  3. Body mass index

    We will measure the change in parent and child body mass index before and after the intervention.

    Time frame: 41 weeks from Baseline

07

Study locations

1 site
  • The Children's Hospital of Philadelphia
    Philadelphia, Pennsylvania 19104, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 5, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01710423
Lead sponsor
Children's Hospital of Philadelphia
Responsible party
Sponsor
First posted
Oct 19, 2012
Start date
Nov 2012
Primary completion
May 2013
Completion
Nov 2013
Last update
Feb 5, 2015

Study contacts

Senbagam Virudachalam, MD, MSHP
principal investigator · Children's Hospital of Philadelphia

Oversight

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

Not currently enrolling

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

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion