- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT03643315
Determinants of Post-Exercise Eating Patterns (DEEP)
Determinants of Post-Exercise Eating Patterns / Alternative Title (Cover): Effect of Pre-meal Activities on Blood Pressure in Healthy Adults
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Verwacht)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
-
-
Singapore, Singapore, Singapore 11760
- Werving
- Clinical Nutrition Research Centre
-
Contact:
- Aaron Sim, PhD
- Telefoonnummer: 64074046
- E-mail: aaron_sim@sics.a-star.edu.sg
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Male
- Inactive (< 90 min of moderate-intensity exercise a week)
- BMI: 23 and above
- Age between 21 to 40 years
- Normal fasting blood glucose levels equal to or less than 5.9 mmol/L
- Non-smoker
- No know allergies or intolerance to food
- Not on any prescribed medication
- No physical disabilities and/or restrictions; not averse to exercising on a stationary bike or treadmill running
- No aversion to blood sampling procedures (e.g. finger prick, cannulation)
Exclusion Criteria:
- Female,
- Smoker,
- Fasting blood glucose > 5.9 mmol/L,
- Resting blood pressure > 140/90 mmHg,
Any major medical/health conditions including
- Diabetes,
- Metabolic disease
- Hypertension,
- Cardiovascular disease,
- Thyroid disorders,
- G6PD deficiency.
- Allergic or intolerant to foods presented in the study.
- Physical disabilities and/or restrictions.
- Individuals that are adverse to exercising on a stationary exercise bike or treadmill.
- Adverse to blood sampling procedures (i.e. cannulation, finger pricks, venepuncture).
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ander
- Toewijzing: Gerandomiseerd
- Interventioneel model: Crossover-opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Exercise and Meal (EX)
The EX protocol will involve a 30 minute acute bout of high intensity intermittent exercise on a stationary exercise bike followed by an ad-libitum test meal.
|
30 minute acute bout of high intensity intermittent exercise followed by ad-libitum meal
|
|
Experimenteel: No-Exercise and Meal (NEX)
The NEX protocol will involve a 30 minute period of rest (to match the exercise period in EX) where participants will be provided a video/movie.
Following this, participants will be provided ad-libitum access to a test meal (as per EX energy intake assessment protocol)
|
30 minute non-exercise period where participants will be watching a video/movie followed by ad-libitum meal
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Ad-libitum amount of food consumed in response to experimental condition: exercise or rest (no exercise).
Tijdsspanne: 3 hours
|
Participants' eating behaviour will be assessed by measuring the total amount of the test meal consumed in each experimental condition.
The test meal will be provided ad-libitum (i.e.
there will be non-restricted access)
|
3 hours
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Appetite-related blood hormone concentration in response to experimental conditions.
Tijdsspanne: 3 hours
|
Venous blood will be sampled for the measurement of a range of appetite-related hormones including Active Ghrelin (pg/ml), Glucagon-like Peptide-1 (GLP-1) (pg/ml), Pancreatic YY (PYY) (pg/ml), Pancreatic Polypeptide (PP) (pg/ml), periodically through the experimental sessions.
|
3 hours
|
|
Metabolic blood variable concentration in response to experimental conditions
Tijdsspanne: 3 hours
|
Venous blood will be sampled for the measurement of metabolic blood variables blood insulin (mmol/L) and blood glucose (mmol/L) periodically through the experimental sessions.
|
3 hours
|
|
Subjective ratings of hunger in response to experimental conditions
Tijdsspanne: 3 hours
|
Self-reported subjective ratings of hunger will be assessed periodically through the experimental session.
Assessed via 100-point visual analogue scales.
|
3 hours
|
|
Subjective ratings of satiation (fullness) in response to experimental conditions
Tijdsspanne: 3 hours
|
Self-reported subjective ratings of satiation (fullness) will be assessed periodically through the experimental session.
Assessed via 100-point visual analogue scales
|
3 hours
|
|
Subjective ratings of desire to eat in response to experimental conditions
Tijdsspanne: 3 hours
|
Self-reported subjective ratings of desire to eat will be assessed periodically through the experimental session.
Assessed via 100-point visual analogue scales
|
3 hours
|
|
Subjective ratings of prospective food consumption in response to experimental conditions
Tijdsspanne: 3 hours
|
Self-reported subjective ratings of prospective food consumption will be assessed periodically through the experimental session.
Assessed via 100-point visual analogue scales.
|
3 hours
|
|
Free-living energy intake (1 day post-experiment) in response to experimental conditions
Tijdsspanne: 1 day
|
1 day free-living energy intake (self-report)
|
1 day
|
|
Free-living physical activity levels intake (1 day post-experiment) in response to experimental conditions
Tijdsspanne: 1 day
|
1 day free-living physical activity levels (physical activity monitors)
|
1 day
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Self-reported tendencies of compensatory health beliefs
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
Influence of self-reported tendencies of compensatory health beliefs on the relationship between experimental conditions and study outcomes. Scale to be used: Compensatory Health Belief (CHB) Scale, CHB Subscales: Substance use, Eating/sleeping habits, Stress and Weight regulation, Ratings on a 5-point agreement scale. Greater scores (summed) indicate greater tendency for an individual to hold compensatory beliefs (for the particular domain/subscale or collectively). |
Assessed at start of study - through study completion - up to 4-5 weeks
|
|
Self-reported tendencies of licensing/reward beliefs
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
Influence of self-reported tendencies of licensing eating behaviour in response to exercise on the relationship between experimental conditions and study outcomes. Scale to be used: Post-Exercise Licensing (PEL)Scale. Ratings on a 7 point agreement scale. Greater scores (averaged) indicate a greater tendency to reward/license in response to exercise. |
Assessed at start of study - through study completion - up to 4-5 weeks
|
|
Self-reported tendencies and motives of compensatory eating behaviour in response to exercise
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
Influence of self-reported tendencies and motives of compensatory eating behaviour in response to exercise on the relationship between experimental conditions and study outcomes Scale to be used: Compensatory Eating Motives Questionnaire (CEMQ) Subscales: Eating for Reward, Eating for Recovery, Eating for Relief (4 point frequency scale) Greater scores (summation of outcome of respective subscales) indicate greater tendency to compensate due to particular motive (respective subscales). |
Assessed at start of study - through study completion - up to 4-5 weeks
|
|
Self-reported assessment of motivation (regulation) to exercise
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
To examine the influence of self-reported motivation to exercise on the relationship between experimental conditions and study outcomes. Scale involve: Behavioural Regulation in Exercise Questionnaire (BREQ) measures the stages of the self-determination contin. Subscales: Amotivation, External regulation, Introjected regulation, Identified regulation, Integrated regulation, Intrinsic regulation.Greater scores (averaged of outcome of respective subscale/items) indicate greater tendency for exercise behaviour to be regulated by particular construct (respective subscale). |
Assessed at start of study - through study completion - up to 4-5 weeks
|
|
Self-reported assessment of motivation to eat healthily
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
To examine the influence of self-reported motivation to adopt healthy eating behaviour on the relationship between experimental conditions and study outcomes. Scale involve: Regulation of Eating Behavioural Scale (REBS). Subscales: Amotivation, External regulation, Introjected regulation, Identified regulation, Integrated regulation, Intrinsic regulation. Greater scores (averaged of outcome of respective subscale/items) indicate greater tendency for eating behaviour to be regulated by particular construct (respective subscale). |
Assessed at start of study - through study completion - up to 4-5 weeks
|
|
Self-reported attitudes towards eating behaviour as assessed by the Three Factor Eating Behaviour Questionnaire (TFEQ-R18)
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
Influence of self-reported attitudes towards eating on the relationship between experimental conditions and study outcomes. Scale involve: Three Factor Eating Behaviour Questionnaire (TFEQ-R18) Subscales: Dietary Restraint, Uncontrolled Eating, Emotional Eating Greater scores (averaged outcome of respective subscale/items) indicate greater likelihood of the behaviour (of construct measure by respective subscales). |
Assessed at start of study - through study completion - up to 4-5 weeks
|
|
Self-reported weight-related behaviour change status as assessed by the Physical Activity Stages of Change Questionnaire
Tijdsspanne: Assessed at start of study - through study completion - up to 4-5 weeks
|
Influence of self-reported weight-related behaviour change status on the relationship between experimental conditions and study outcomes. Scale involve: Physical Activity Stages of Change Questionnaire. Scores (based on scoring algorithm) will indicate participants' current stage of motivational readiness for change specific to physical activity. Greater score (1-5 representing five stages of change) indicates physical activity status and intent to be active. |
Assessed at start of study - through study completion - up to 4-5 weeks
|
Medewerkers en onderzoekers
Medewerkers
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- 2017/01034
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
Study Protocol Statistical Analysis Plan (SAP) Informed Consent Form (ICF)
Will be made available to other researchers upon request
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .