A Pilot Laboratory Study Investigating How Physical Tasks and Hunger Affect Taste Perception
26. december 2012 opdateret af: 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.
Studieoversigt
Status
Ukendt
Betingelser
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
120
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Rhode Island
-
Providence, Rhode Island, Forenede Stater, 02903
- Rekruttering
- The Miriam Hospital's Weight Control and Diabetes Research Center
-
Underforsker:
- Rena R Wing, PhD
-
Kontakt:
- Xiaomeng Xu, PhD
- Telefonnummer: 401-793-8237
- E-mail: xxu1@lifespan.org
-
Kontakt:
- Tricia Leahey, PhD
- Telefonnummer: 401-793-8947
- E-mail: tleahey@lifespan.org
-
Ledende efterforsker:
- Xiaomeng Xu, PhD
-
Underforsker:
- Tricia M Leahey, PhD
-
Underforsker:
- Katherine Boguszewski, BA
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: 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
|
|
Aktiv komparator: 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
|
|
Aktiv komparator: 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).
|
|
Aktiv komparator: 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).
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
physical perseverance
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
food preference
Tidsramme: 1 hour
|
Food preference measured via participant's reported ratings after tasting different food.
|
1 hour
|
|
Amount of food eaten
Tidsramme: 1 hour
|
Amount of food that participants eat will be measured via a food scale at the end of the study.
|
1 hour
|
|
Mood
Tidsramme: 1 hour
|
Participant's subjective mood will be measured using a mood questionnaire (PANAS).
|
1 hour
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Xiaomeng Xu, PhD, The Miriam Hospital
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. januar 2012
Primær færdiggørelse (Forventet)
1. august 2013
Studieafslutning (Forventet)
1. august 2013
Datoer for studieregistrering
Først indsendt
19. december 2012
Først indsendt, der opfyldte QC-kriterier
26. december 2012
Først opslået (Skøn)
1. januar 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
1. januar 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
26. december 2012
Sidst verificeret
1. december 2012
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 2T32HL076134-06XX (U.S. NIH-bevilling/kontrakt)
- 2T32HL076134-06 (U.S. NIH-bevilling/kontrakt)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .