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

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:
        • Contact:
        • 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.

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

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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