- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01758302
A Pilot Laboratory Study Investigating How Physical Tasks and Hunger Affect Taste Perception
December 26, 2012 updated by: The Miriam Hospital
This one time pilot laboratory study focuses on examining the relationship between different types of physical tasks and taste perception of high and low-calorie foods among hungry individuals.
Study Overview
Status
Unknown
Conditions
Study Type
Interventional
Enrollment (Anticipated)
120
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
-
-
Rhode Island
-
Providence, Rhode Island, United States, 02903
- Recruiting
- The Miriam Hospital's Weight Control and Diabetes Research Center
-
Sub-Investigator:
- Rena R Wing, PhD
-
Contact:
- Xiaomeng Xu, PhD
- Phone Number: 401-793-8237
- Email: xxu1@lifespan.org
-
Contact:
- Tricia Leahey, PhD
- Phone Number: 401-793-8947
- Email: tleahey@lifespan.org
-
Principal Investigator:
- Xiaomeng Xu, PhD
-
Sub-Investigator:
- Tricia M Leahey, PhD
-
Sub-Investigator:
- Katherine Boguszewski, BA
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Willing to travel to laboratory around lunchtime for the study
- Willing to abstain from eating and drinking caloric beverages for at least 4 hours prior to completing the study
- Typically eats lunch
Exclusion Criteria:
- Diabetes, eating disorder, or any other condition that makes it unadvisable for participant to refrain from eating or drinking caloric beverages for 4 hours.
- Food allergies that would prevent participants from eating chocolate chip cookies or vegetables
- Pregnant or lactating
- Typically goes for longer than 5 hours (not counting sleep time) between meals and snacks
- Physical disabilities that would make it difficult for the participant to walk or to use their hands to grasp objects
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: No physical task + Taste cookies
Participants in this arm do not engage in a physical activity task.
They are asked to taste test chocolate chip cookies.
|
Participants are asked to taste test chocolate chip cookies
As a control, for 2 of the arms, participants are not asked to engage in a physical task
|
|
Active Comparator: No physical task + Taste vegetable
Participant does not complete a physical activity.
Asked to taste test raw celery or radishes.
|
As a control, for 2 of the arms, participants are not asked to engage in a physical task
Participants are asked to taste test raw celery or radishes
|
|
Active Comparator: Simple physical task + Taste vegetables
Participants are asked to complete a simple physical task and are asked to taste test raw celery or radishes.
|
Participants are asked to taste test raw celery or radishes
Participants are asked to complete a 1-time simple physical task that is not challenging nor novel (moving small objects across a room).
|
|
Active Comparator: Complex physical task + Taste vegetables
Participants complete a more complex physical task that is novel and challenging.
They are asked to taste test raw celery or radishes.
|
Participants are asked to taste test raw celery or radishes
Participants are asked to complete a 1-time physical task that is low intensity but somewhat complex (involves a novel request to move objects in a way that is challenging and requires some coordination).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
physical perseverance
Time Frame: 1 hour
|
as measured via maintained grip using a hand dynamometer on the dominant hand and set to 70% of participant's maximum grip strength
|
1 hour
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
food preference
Time Frame: 1 hour
|
Food preference measured via participant's reported ratings after tasting different food.
|
1 hour
|
|
Amount of food eaten
Time Frame: 1 hour
|
Amount of food that participants eat will be measured via a food scale at the end of the study.
|
1 hour
|
|
Mood
Time Frame: 1 hour
|
Participant's subjective mood will be measured using a mood questionnaire (PANAS).
|
1 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Xiaomeng Xu, PhD, The Miriam Hospital
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
January 1, 2012
Primary Completion (Anticipated)
August 1, 2013
Study Completion (Anticipated)
August 1, 2013
Study Registration Dates
First Submitted
December 19, 2012
First Submitted That Met QC Criteria
December 26, 2012
First Posted (Estimate)
January 1, 2013
Study Record Updates
Last Update Posted (Estimate)
January 1, 2013
Last Update Submitted That Met QC Criteria
December 26, 2012
Last Verified
December 1, 2012
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2T32HL076134-06XX (U.S. NIH Grant/Contract)
- 2T32HL076134-06 (U.S. NIH Grant/Contract)
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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