- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03750019
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
Status
Completed
Conditions
Intervention / Treatment
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
-
-
-
Liverpool, United Kingdom
- University of Liverpool
-
-
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.
Sponsor
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
Keywords
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
-
Individual Participant Data Set
Information identifier: 10.5255/UKDA-SN-853370
-
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.
Clinical Trials on Overweight and Obesity
-
Washington University School of MedicinePatient-Centered Outcomes Research Institute; Pennington Biomedical Research... and other collaboratorsCompletedOvernutrition | Nutrition Disorders | Overweight | Body Weight | Pediatric Obesity | Body Weight Changes | Childhood Obesity | Weight Gain | Adolescent Obesity | Obesity, Childhood | Overweight and Obesity | Overweight or Obesity | Overweight AdolescentsUnited States
-
Institut Investigacio Sanitaria Pere VirgiliCompletedObesity, Childhood | Overweight and Obesity | Overweight, ChildhoodSpain
-
National University Health System, SingaporeActive, not recruitingObesity | Overweight and/or Obesity | Overweight or Obese Adults | Overweight , ObesitySingapore
-
Holbaek SygehusUniversity of Copenhagen; University of Florida; University of Minnesota; Hebrew... and other collaboratorsRecruitingChildhood Overweight and ObesityDenmark
-
National Taiwan University HospitalCompleted
-
PfizerNot yet recruitingObesity | Overnutrition | Nutrition Disorders | Overweight | Body Weight | Overweight or Obesity | Overweight and/or Obesity | Nutritional and Metabolic DiseasesUnited States
-
University of Texas Southwestern Medical CenterChildren's Medical Center DallasRecruitingPediatric Obesity | Pediatric Overweight | Overweight , ObesityUnited States
-
Universidade do Extremo Sul Catarinense - Unidade...RecruitingObesity | Overweight and Obesity | Obesity; Endocrine | Overweight, Obesity and Other HyperalimentationBrazil
-
Mexican National Institute of Public HealthUNICEFCompleted
-
Universidade do PortoFundação para a Ciência e a Tecnologia; Administração Regional de Saúde do... and other collaboratorsCompletedOverweight and ObesityPortugal
Clinical Trials on Satisfying rehearsal task
-
Arizona State UniversityShanghai Xuhui Clover Children Healthy Garden; Jingdezhen Kindkids Autism Rehabilitation... and other collaboratorsTerminated
-
Philipps University MarburgRecruitingSocial Anxiety | Social PhobiaGermany
-
Philipps University MarburgRecruitingPublic Speaking Fear | Public Speaking AnxietyGermany
-
University Hospital, GenevaCompletedPTSD | Nightmares, REM-Sleep TypeSwitzerland
-
University Hospital, GenevaCompletedNightmares, REM-Sleep TypeSwitzerland
-
University of California, Los AngelesCompleted
-
Kessler FoundationNew Jersey Commission on Brain Injury ResearchCompletedMotor Learning in TBIUnited States
-
GGZ CentraalUtrecht UniversityCompletedPersonality Disorders | Mood Disorders | Anxiety Disorders | NightmaresNetherlands
-
Northwestern UniversityUniversity of PennsylvaniaCompletedAssess Fidelity to Cognitive-behavioral Therapy for Youth