Remembered Meal Satisfaction, Satiety and Later Snack Food Intake

November 19, 2018 updated by: Eric Robinson, University of Liverpool

Remembered Meal Satisfaction, Satiety and Later Snack Food Intake: A Laboratory Study

This study examined whether remembered meal satisfaction (encompassing memory for meal liking and satiety) can be manipulated in the laboratory and whether this influences later food intake.

Study Overview

Detailed Description

This study examined whether remembered meal satisfaction (encompassing memory for meal liking and satiety) can be manipulated in the laboratory and whether this influences later food intake. In a between-subjects design participants consumed a fixed lunch and then rehearsed the satisfying or dissatisfying aspects of the meal, or a neutral experience (control), in order to manipulate memory for meal satisfaction. Three hours later, in a second visit to the laboratory, participants completed a bogus taste-test to measure food intake and meal memory measures.

Study Type

Interventional

Enrollment (Actual)

146

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 Locations

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

18 years to 60 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Fluent English
  • Not taking medication that affects appetite
  • No known history of food allergies or disordered eating

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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Satisfying rehearsal
Participants completed the satisfying rehearsal task where they rehearsed the satisfying aspects of the lunchtime meal.
Participants rehearsed satisfying aspects of the lunchtime meal they just ate.
EXPERIMENTAL: Dissatisfying rehearsal
Participants completed the dissatisfying rehearsal task where they rehearsed the dissatisfying aspects of the lunchtime meal.
Participants rehearsed dissatisfying aspects of the lunchtime meal they just ate.
ACTIVE_COMPARATOR: Neutral rehearsal
Participants completed the neutral rehearsal task where they rehearsed their journey to campus that day.
Participants rehearsed their journey to campus that day.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ad libitum snack intake
Time Frame: Measured during second visit that took place 3 hours after the baseline visit
Energy intake (kcal) measured from a bogus taste-test task. Lower intake in those in the satisfying rehearsal condition compared to the control condition and greater intake in the dissatisfying rehearsal condition compared to the control condition were expected.
Measured during second visit that took place 3 hours after the baseline visit

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Memory for general satisfaction
Time Frame: Measured during second visit that took place 3 hours after the baseline visit
Memory for general satisfaction with the lunchtime meal was measured via five questions: 'Overall, how satisfying did you find the lunchtime meal?', 'Overall, how dissatisfying did you find the lunchtime meal?', 'I liked the lunchtime meal', 'How satisfied were you with the taste of the lunchtime meal?' and 'How dissatisfied were you with the taste of the lunchtime meal?'. Responses were measured using 100-point visual analogue scales with anchors 'not at all' and 'extremely' (0-100). A higher score in those in the satisfying rehearsal condition compared to the control condition and a lower score in the dissatisfying rehearsal condition compared to the control condition were expected.
Measured during second visit that took place 3 hours after the baseline visit
Memory for satisfaction with meal satiety
Time Frame: Measured during second visit that took place 3 hours after the baseline visit
Memory for general satisfaction with the lunchtime meal was measured via two questions: 'How satisfied were you with how filling the lunchtime meal was?' and 'How dissatisfied were you with how filling the lunchtime meal was?'. Responses were measured using 100-point visual analogue scales with anchors 'not at all' and 'extremely' (0-100). A higher score in those in the satisfying rehearsal condition compared to the control condition and a lower score in the dissatisfying rehearsal condition compared to the control condition were expected.
Measured during second visit that took place 3 hours after the baseline visit

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hunger before lunch
Time Frame: Measured before lunch (during baseline visit)
Hunger before lunch was measured via a single question asking 'How hungry do you feel right now?'. Responses were measured via a 100-point visual analogue scale with anchors 'not at all' and 'extremely'. No directional hypothesis was made for this outcome.
Measured before lunch (during baseline visit)
Hunger after lunch
Time Frame: Measured after lunch (during baseline visit)
Hunger before lunch was measured via a single question asking 'How hungry do you feel right now?'. Responses were measured via a 100-point visual analogue scale with anchors 'not at all' and 'extremely'. No directional hypothesis was made for this outcome.
Measured after lunch (during baseline visit)
Hunger before the bogus taste-test
Time Frame: Measured before the bogus taste-test (in second visit that took place 3 hours after the baseline visit)
Hunger before lunch was measured via a single question asking 'How hungry do you feel right now?'. Responses were measured via a 100-point visual analogue scale with anchors 'not at all' and 'extremely'. No directional hypothesis was made for this outcome.
Measured before the bogus taste-test (in second visit that took place 3 hours after the baseline visit)
Hunger after the bogus taste-test
Time Frame: Measured after the bogus taste-test (in second visit that took place 3 hours after the baseline visit)
Hunger before lunch was measured via a single question asking 'How hungry do you feel right now?'. Responses were measured via a 100-point visual analogue scale with anchors 'not at all' and 'extremely'. No directional hypothesis was made for this outcome.
Measured after the bogus taste-test (in second visit that took place 3 hours after the baseline visit)

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)

August 7, 2017

Primary Completion (ACTUAL)

December 8, 2017

Study Completion (ACTUAL)

December 8, 2017

Study Registration Dates

First Submitted

November 14, 2018

First Submitted That Met QC Criteria

November 19, 2018

First Posted (ACTUAL)

November 21, 2018

Study Record Updates

Last Update Posted (ACTUAL)

November 21, 2018

Last Update Submitted That Met QC Criteria

November 19, 2018

Last Verified

November 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RETH000955

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

IPD is available on the UK Data Service and the study protocol is available on the Open Science Framework.

IPD Sharing Time Frame

Data is already available.

IPD Sharing Access Criteria

There are no restrictions on access to the IPD or study protocol.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Study Data/Documents

  1. Individual Participant Data Set
    Information identifier: 10.5255/UKDA-SN-853370
  2. Study Protocol
    Information identifier: 10.17605/OSF.IO/WYCKJ

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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