- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02764177
Resistance Exercise, Recovery Drinks and Appetite
5. maj 2016 opdateret af: Lewis James, Loughborough University
Effect of Recovery Drink Composition Consumed After Resistance Exercise on Subsequent Appetite and Energy Intake
Whilst the effects of manipulating the macronutrient content of foods on appetite and energy intake has been relatively well studied at rest, little is known about these responses in a post-exercise context.
The effect of post-exercise nutrition on recovery from or adaptation to exercise has been well studied.
However, many exercisers do so for weight management and thus any post-exercise nutrition might impact on energy balance and might need to be carefully considered.
This study will examine the impact of manipulating the composition of a recovery drink consumed after resistance exercise on subsequent appetite and energy intake.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Subjects perform a bout of lower body resistance exercise lasting ~50 min and immediately post-exercise they consume one of two recovery drinks over a 5 min period.
Over the next 60 min subjective appetite responses will be measured and then 60 min after drink ingestion, subjects will consume an ad-libitum meal.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
15
Fase
- Ikke anvendelig
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 60 år (Voksen)
Tager imod sunde frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Generally fit and healthy
- Use resistance exercise as part of weekly training
- Weight stable in previous 6 months
Exclusion Criteria:
- Smoker
- History of gastric, digestive, cardiovascular or renal disease
- Lactose, dairy, gluten intolerances or allergies
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: Crossover opgave
- Maskning: Tredobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Protein
In this arm the subjects were provided with a PROTEIN drink to consume after exercise.
This protein drink contained whey protein isolate that provided 0.3 g/ kg body mass of protein.
|
The protein drink was administered during this trial
|
|
Eksperimentel: Carbohydrate
In this arm the subjects were provided with a CARBOHYDRATE drink to consume after exercise.
This carbohydrate drink was energy matched to the protein drink in the other arm of the experiment.
|
The carbohydrate drink was administered in this trial
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Ad-libitum energy intake
Tidsramme: 65 min post-exercise
|
Assessed via a homogenous pasta meal
|
65 min post-exercise
|
|
Subjective appetite (hunger)
Tidsramme: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
|
Subjective appetite (fullness)
Tidsramme: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
|
Subjective appetite (desire to eat)
Tidsramme: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
|
Subjective appetite (prospective food consumption)
Tidsramme: 150 min
|
Assessed via 100 mm visual analogue scales
|
150 min
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Pleasantness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Aftertaste of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Saltiness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Bitterness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Sweetness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Creaminess of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Thickness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Stickiness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Fruitiness of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Refreshment of study drinks
Tidsramme: Immediately after drinking
|
Assessed via 100 mm visual analogue scales
|
Immediately after drinking
|
|
Eating rate
Tidsramme: 65 min post-exercise
|
mean eating rate determined at ad-libitum meal
|
65 min post-exercise
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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. oktober 2014
Primær færdiggørelse (Faktiske)
1. december 2015
Studieafslutning (Faktiske)
1. december 2015
Datoer for studieregistrering
Først indsendt
4. maj 2016
Først indsendt, der opfyldte QC-kriterier
4. maj 2016
Først opslået (Skøn)
6. maj 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
9. maj 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
5. maj 2016
Sidst verificeret
1. maj 2016
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- R15-P106
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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