The Influence of Fictitious Peers in a Social Media Intervention for Downsizing Portions: The Smart Snacking Studies

August 20, 2019 updated by: Charlotte Evans, University of Leeds
The 2 interventions aimed to examine whether peer-led nudging on social media may be a way of influencing young adults and adolescents to reduce their self-reported ideal portion sizes of high energy-dense snacks and sugar-sweetened beverages.

Study Overview

Status

Completed

Detailed Description

Two pilot interventions were conducted which examined the influence of peer-led nudging on social media as a way of influencing self-reported ideal portions of high energy-dense snacks and sugar-sweetened beverages. In both interventions the peers posted images of 'their' snacks and beverages, which constituted the recommended portion, onto an Instagram account. The peers also posted images relating to portion sizes, calories and other information related to health but not specifically portion size. It was hypothesised that viewing images of peers' snacks would influence the participants to reduce their own snack and beverage ideal portion sizes.

Intervention 1 lasted for 2 weeks and recruited young adults and used a within-subjects design. Intervention 2 lasted for 4 weeks and recruited adolescents and used a between-subjects design. In intervention 2, participants were randomly assigned to either the intervention or the control condition. This protocol focusses on intervention 2.

In both interventions, participants in the intervention condition were added to an Instagram account and were required to visit Instagram daily and to like all posts. All participants (intervention and control) completed a survey at baseline and at the end of the intervention, and completed quizzes at the end of each week.

Study Type

Interventional

Enrollment (Actual)

44

Phase

  • Not Applicable

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

13 years to 16 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

13-16 years old (intervention 2)

Exclusion Criteria:

  • Younger than 13 or older than 16 (intervention 2).
  • History of or current eating disorder

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Smart snacking intervention
In intervention 2 participants took part in a 4-week intervention on Instagram. Participants saw images of fictitious peers' snacks or beverages three times per week, and saw snack information images three times per week. Peer snack images were posted on days 2,4 and 6 of each week, and snack information images were posted on days 1,3 and 5 of each week. Images were posted between 10-11am each day. Participants also completed quizzes related to snacking at the end of weeks 1-3. Participants completed a survey at baseline and intervention end to assess their ideal portion sizes to allow for examination of the effectiveness of the intervention.
The smart snacking intervention aimed to examine whether peer-led nudging on social media influenced adolescents to reduce their self-reported ideal portion sizes for a variety of HED snacks and SSBs. In intervention 2, participants were randomly allocated to the intervention or control condition, and their ideal portion sizes were assessed through a survey at baseline and intervention end.
No Intervention: Control
Participants in the control received no intervention. They completed the questionnaires at the end of weeks 1, 2 and 3, and also completed the surveys at baseline and intervention end.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported ideal portion size
Time Frame: Baseline at the beginning of week 1 and intervention end at the end of week 4.
Questionnaire measuring participants' self-reported ideal portion size. The aim of the intervention was to reduce the ideal portion size. Participants were provided with different images of food. For each image, judgements were made on whether the portion was 'too little', 'slightly less than I would eat', 'just right', 'slightly more than I would eat', or 'too much'.
Baseline at the beginning of week 1 and intervention end at the end of week 4.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceptions of peers' ideal portion sizes
Time Frame: Baseline at the beginning of week 1 and intervention end at the end of week 4
Questionnaire measuring participants' perceptions of their peers' ideal portion sizes. Participants were provided with images of different energy dense foods. For each image, judgements were made on whether the portion was 'too little', 'slightly less than I would eat', 'just right', 'slightly more than I would eat', or 'too much'. The aim of the intervention was to reduce the ideal portion size.
Baseline at the beginning of week 1 and intervention end at the end of week 4
Participants liking and frequency of consumption of high energy dense snack foods and sugar-sweetened beverages
Time Frame: Baseline at the beginning of week 1 and intervention end at the end of week 4
Questionnaire measuring participants' liking and frequency of consumption. Participants' reported frequency of consumption for and liking of each item were assessed based on questions used by Stok, De Ridder, De Vet, & De Wit (2014). Mean frequency and liking scores were calculated for HED snacks and SSBs. A low score for frequency indicated that the item was not eaten frequently, a low score for liking indicated that the item was not liked.
Baseline at the beginning of week 1 and intervention end at the end of week 4
Participants' intentions regarding their portions
Time Frame: Baseline at the beginning of week 1 and intervention end at the end of week 4
Questionnaire measuring participants' intentions. Participants' reported intentions which were assessed based on questions used by Stok, De Ridder, De Vet, & De Wit (2014). Mean intention scores were calculated for HED snacks and SSBs. A low score for intention score indicated that participants did not intend to change their behaviour.
Baseline at the beginning of week 1 and intervention end at the end of week 4

Collaborators and Investigators

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

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 (Actual)

December 8, 2016

Primary Completion (Actual)

June 1, 2017

Study Completion (Actual)

June 1, 2017

Study Registration Dates

First Submitted

May 16, 2019

First Submitted That Met QC Criteria

August 20, 2019

First Posted (Actual)

August 22, 2019

Study Record Updates

Last Update Posted (Actual)

August 22, 2019

Last Update Submitted That Met QC Criteria

August 20, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 17-0111/ 17-0094

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Data will be available on request. Only anonymised data will be available.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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