- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02416882
Exercise Genes: Genomic Association With Exercise Reinforcement (ExGenes)
18. juli 2019 opdateret af: James Roemmich, USDA Grand Forks Human Nutrition Research Center
This study tests whether different physical activity patterns are linked an individual's genes.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The investigators propose that an individual's genetics are one factor that may be associated with the motivating aspect or attractiveness of exercise and therefore the choice to exercise rather than be sedentary.
They propose to study the association of the genomic signatures with the reinforcing (motivating) value of different types of exercise.
This has never been investigated and may uncover underlying mechanisms that would help to understand individual differences in exercise motivation.
The ultimate impact of this work is a greater number of Americans being physically active, meeting the United States Department of Agriculture (USDA) dietary guidelines for physical activity, and maintaining a healthy body weight.
This study will be funded and undertaken at the Grand Forks Human Nutrition Research Center (GFHNRC).
The purpose will be to assess genetic underpinnings of the motivating value of resistance and aerobic exercise, and to determine whether the motivating value of aerobic and resistance exercise are associated with usual participation in these modes of exercise.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
88
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
North Dakota
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Grand Forks, North Dakota, Forenede Stater, 58203
- USDA Grand Forks Human Nutrition Research Center
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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 til 50 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- BMI within 18.5-35.0 kg/m2
- Healthy enough to exercise
- Active or inactive (not exercising at this time)
Exclusion Criteria:
- Taking any drugs that affect energy expenditure (e.g., thyroid, glucose-lowering drugs)
- Have gained or lost more than 5% of body weight over the past 6 months
- Use tobacco
- Pregnant or lactating or plan to become pregnant in the next 6 months
- Have any health conditions that prevent the individual from safely exercising (e.g., cardiovascular, liver, endocrine, or pulmonary diseases)
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Andet: Aerobic Exercise vs Sedentary Option
Relative Reinforcing Value of aerobic exercise versus sedentary activity will be determined.
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Subjects will sample and rate their liking of three cardiovascular machines (treadmill, cycle ergometer, elliptical step ergometer) to determine which one will be used during the test.
Subjects will rate their liking of three sedentary activities (reading magazines, playing puzzles, completing word games) as an alternative to exercise.
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Andet: Resistance Exercise vs Sedentary Option
Relative Reinforcing Value of resistance exercise versus sedentary activity will be determined.
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Subjects will rate their liking of three sedentary activities (reading magazines, playing puzzles, completing word games) as an alternative to exercise.
Subjects will sample and rate their liking of three different resistance training circuits (upper body, lower body, core) to determine which one will be used during the test.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Relative reinforcing value (RRV) of physical activity
Tidsramme: Week 0 (Cross-sectional)
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RRV of physical activity will be assessed by evaluating the number of responses (mouse button presses) a subject is willing to complete to gain access to physical activity or a sedentary alternative.
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Week 0 (Cross-sectional)
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Preference for intense physical activity and tolerance for exercise discomfort
Tidsramme: Week 0 (Cross-sectional)
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Preference for intense physical activity and tolerance for exercise discomfort will be assessed by self-report questionnaire responses.
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Week 0 (Cross-sectional)
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Genotypes of 23 small nucleotide polymorphisms (SNPs) previously identified to influence central dopamine release or uptake, reward, or physical activity
Tidsramme: Week 0 (Cross-sectional)
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SNP genotyping will be performed on 3-5 ml samples of whole blood collected in ethylenediaminetetraacetic acid (EDTA)-containing tubes followed by allelic-discrimination analysis for the amplification and identification of each SNP.
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Week 0 (Cross-sectional)
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: James N Roemmich, PhD, USDA Grand Forks Human Nutrition Research Center
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 (Faktiske)
1. april 2015
Primær færdiggørelse (Faktiske)
1. november 2015
Studieafslutning (Faktiske)
1. december 2015
Datoer for studieregistrering
Først indsendt
2. april 2015
Først indsendt, der opfyldte QC-kriterier
9. april 2015
Først opslået (Skøn)
15. april 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
23. juli 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. juli 2019
Sidst verificeret
1. juli 2019
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- GFHNRC405
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Ingen
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 .
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