Supper Heroes: Examining the Impact of an Online Eating Intervention for Families

April 7, 2025 updated by: Jess Haines, University of Guelph

Supper Heroes: Randomized Controlled Trial to Examine the Impact of an Online Environmentally Friendly Eating Intervention for Families

This study will examine the effectiveness of the online family-based program focused on sustainable eating compared to weekly emails about environmentally friendly behaviours.

Study Overview

Detailed Description

The investigators will conduct a family-level RCT following CONSORT guidelines: families will be randomly allocated into control and intervention groups. The control group will receive an email once a week for 7 weeks with information about environmentally friendly habits.

The intervention group will participate in the 7-week online Supper Heroes program consisting of 7 online "missions" completed over 7 weeks. Each mission includes tasks for families to complete, including reading infographics, watching short videos, participating in family-based activities, and sharing their progress. Parents will receive 2 text messages each week with information about the program. Families will also receive a toolkit to support their participation which will contain cookbooks, a potato brush, grocery planning tools, and a note that orients them to what is included. It will take approximately 1-2 hours per mission to complete all activities.

  • Infographics: Each mission will contain brief, 1-2-page infographics for families to read. Topics are related to the mission theme for that week. For example, families may learn about tips for grocery shopping and meal planning as well as information about plant-based proteins.
  • Videos: Similar to the infographics, short, 1-5-minute online videos will be related to the theme of the mission participants are completing. For example, families will watch a short, animated video about grocery shopping.
  • Family-based activities: During each mission, participants will be invited to participate in a family-based activity such as follow-along cooking videos, doing an audit of their fridge, and creating a grocery shopping list.
  • Sharing: Families will be asked to share their experiences for each mission on an online community share board by providing a photo and/or text.

Study Type

Interventional

Enrollment (Estimated)

330

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Ontario
      • Guelph, Ontario, Canada, N1G 2W1
        • University of Guelph
        • Contact:
        • Contact:
          • Jess Haines, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • have at least one child 9-12 years old
  • live in Ontario, Canada
  • have access to the internet
  • can respond to English surveys

Exclusion Criteria:

  • parent(s) with prior nutrition and food education (e.g., degree in nutrition, culinary arts training)
  • families with food allergies that would prevent them from participating in the intervention (e.g., soy products, beans or lentils)
  • families who are vegetarian or vegan

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control Group
Families randomized to the control group will receive weekly emails for 7 weeks about environmentally friendly habits.
Families randomized to the control group will receive monthly emails for 6 months about environmentally friendly habits.
Experimental: Supper Heroes online environmentally friendly eating intervention for families
Families randomized to the intervention group will complete a 7-week Supper Heroes program that includes activities focused on making more meals at home, reducing food waste, and eating more plant-based foods.
Families randomized to the intervention group will complete a 7-week Supper Heroes program that includes activities focused on making more meals at home, reducing food waste, and eating more plant-based foods.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Decrease in avoidable food waste
Time Frame: 15 months

The amount of avoidable food waste generated is measured as the difference in weight (grams) between baseline (T0), post-intervention/control (T1), and 6-month follow-up (T2), as assessed by weighed food waste diaries. Participants will complete a food waste diary using a provided kitchen scale and detailed instructions on how to do so. The amount of avoidable food waste will be compared between participants in the Supper Heroes intervention group and those in the control group.

Measurement Tool: Food waste diary and kitchen scale.

Unit of Measure: Families will be asked to list all food thrown away, the weight of the food (gams) and the reason the food was thrown away (e.g., it went bad) for 7 days.

Time Points: Baseline (T0): post-intervention/control (T1 - after completion of either intervention or control activities, 7 weeks); follow-up (T2 - 6 months after completing the intervention or control activities).

15 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Increased intake of plant-based foods among parents and children.
Time Frame: 15 months

The amount of plant-based foods consumed by parents and children is measured as the mean servings of plant-based foods, as assessed by a web-based food frequency questionnaire. This will be compared between participants in the Supper Heroes intervention group and those in the control group.

Measurement Tool: Food frequency questionnaire adapted from Canadian Diet History Questionnaire II (National Cancer Institute, n.d.)

Unit of Measure: Servings of plant-based foods consumed per day

Time Points: Baseline (T0): post-intervention/control (T1 - after completion of either intervention or control activities, 7 weeks); follow-up (T2 - 6 months after completing the intervention or control activities).

National Cancer Institute. (n.d.). Diet History Questionnaire (DHQ2). U.S. Department of Health and Human Services. Retrieved April 3, 2025, from https://epi.grants.cancer.gov/dhq2/

15 months
Decreased intake of red and processed meats among parents and children.
Time Frame: 15 months

The amount of red and processed meats consumed by parents and children, measured as the average daily intake (servings) of red and processed meats, as assessed by a web-based food frequency questionnaire. This will be compared between participants in the Supper Heroes intervention group and those in the control group.

Measurement Tool: Food frequency questionnaire adapted from Canadian Diet History Questionnaire II (National Cancer Institute, n.d.)

Unit of Measure: Servings of red and processed meats consumed per day

Time Points: Baseline (T0): post-intervention/control (T1 - after completion of either intervention or control activities, 7 weeks); follow-up (T2 - 6 months after completing the intervention or control activities).

National Cancer Institute. (n.d.). Diet History Questionnaire (DHQ2). U.S. Department of Health and Human Services. Retrieved April 3, 2025, from https://epi.grants.cancer.gov/dhq2/

15 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluate mechanisms of behaviour change.
Time Frame: 15 months

The changes in parents' and children's attitudes, subjective norms, and perceived behavioral control, measured using items previously validated in the feasibility study (Eckert et al., 2025), as potential mediators of the intervention effects on the primary and secondary outcomes. These constructs will be assessed before and after the intervention to determine their role in mediating changes in behavior, such as the intake of plant-based foods and red/processed meats.

Time Points: Baseline (T0): post-intervention/control (T1 - after completion of either intervention or control activities, 7 weeks).

Eckert KF, Agostinelli J, Laila A, Alexander C, Parizeau K, von Massow M, Duncan AM, Hesketh KD, Ma DWL, Haines J. Feasibility, acceptability, and preliminary impact of "Supper Heroes", a family-based sustainable diet intervention. Appetite. 2025 Feb 1;206:107849. doi: 10.1016/j.appet.2025.107849. Epub 2025 Jan 7. PMID: 39788349.

15 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jess Haines, PhD, University of Guelph

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

July 1, 2025

Primary Completion (Estimated)

April 1, 2027

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

March 27, 2025

First Submitted That Met QC Criteria

April 7, 2025

First Posted (Actual)

April 15, 2025

Study Record Updates

Last Update Posted (Actual)

April 15, 2025

Last Update Submitted That Met QC Criteria

April 7, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Supper Heroes: RCT

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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