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De klinische studie NCT06366399 voor Diabetes mellitus, type 2, Insulineresistentie, Glucose-intolerantie, Slaapverstoring, Overgewicht of Obesitas, Insulinegevoeligheid is recruterend. Bekijk de kaartweergave van de Klinische Studies Radar en de AI-ontdekkingstools voor alle details. Of stel hier een vraag. | ||
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Universiteit van UtahThe Acute T-Rex (Timing of Resistance Exercise) Study
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De klinische studie NCT06366399 is een interventioneel studie bij Diabetes mellitus, type 2, Insulineresistentie, Glucose-intolerantie, Slaapverstoring, Overgewicht of Obesitas, Insulinegevoeligheid met de status recruterend. Het doel is om 20 deelnemers te includeren vanaf 15 november 2023. De studie wordt geleid door de Universiteit van Utah en de voltooiing is gepland op 31 december 2025. Laatste update op ClinicalTrials.gov: 3 april 2025.
Beknopte samenvatting
The primary aim of this study is to evaluate if a single bout of AM vs PM resistance exercise has different effects on insulin sensitivity and sleep. A randomized cross-over trial be used to compare resistance exercise at two different times of the day. Each condition will take place in a laboratory setting. Each condition will consist of exercise, overnight sleep, and oral glucose tolerance tests the following day. The AM exercise will occur ~1.5 hours after habitual wake, and PM exercise will occur ~11 hours after habitual wake. After a 2-6 week washout, participants will complete the other condition. The hypothesis is that PM exercise will be more beneficial than AM exercise in improving insulin sensitivity. This study could identify if there is a better time of day to perform resistance exercise to decrease risk of developing Type 2 Diabetes Mellitus.
Officiële titel
Timing (AM v PM) of Acute Resistance Exercise on Glycemic Control in Older Adults: The Acute T-Rex Study
Aandoeningen
Diabetes mellitus, type 2InsulineresistentieGlucose-intolerantieSlaapverstoringOvergewicht of ObesitasInsulinegevoeligheidAndere studie-ID's
- 00156659
NCT-ID
Startdatum (Werkelijk)
2023-11-15
Laatste update geplaatst
2025-04-03
Verwachte einddatum
2025-12-31
Inschrijving (Geschat)
20
Studietype
Interventioneel
FASE
N.v.t.
Status
Recruterend
Trefwoorden
Resistance Exercise
Strength-training
Sleep
Circadian Rhythm
Strength-training
Sleep
Circadian Rhythm
Primaire doel
Preventie
Toewijzing
Gerandomiseerd
Interventiemodel
Cross-over
Blindering
Dubbelblind
Armen / Interventies
| Deelnemersgroep/Studiearm | Interventie/Behandeling |
|---|---|
ExperimenteelAM Resistance Exercise Resistance Exercise intervention taking place in the AM | Resistance Exercise Timing 1 resistance exercise session consisting of 3 sets, 10 repetitions per set, on 12 different exercises |
ExperimenteelPM Resistance Exercise Resistance Exercise intervention taking place in the PM | Resistance Exercise Timing 1 resistance exercise session consisting of 3 sets, 10 repetitions per set, on 12 different exercises |
Primaire uitkomst
Secundaire uitkomst
| Uitkomstmaat | Beschrijving van de uitkomstmaat | Tijdsbestek |
|---|---|---|
Insulin sensitivity | Insulin sensitivity will be calculated using the Matsuda Insulin Sensitivity Index | 1 day |
| Uitkomstmaat | Beschrijving van de uitkomstmaat | Tijdsbestek |
|---|---|---|
Sleep Duration | Sum of time spent in stage 1, stage 2, stage 3 and rapid eye movement stage (REM) as assessed via polysomnography. | 1 day |
Geschiktheidscriteria
Leeftijd van deelnemers
Volwassene, Oudere volwassene
Minimumleeftijd
50 Years
Geslachten die in aanmerking komen voor de studie
Allen
- Men and women, all ethnicities, aged 50-74 years
- BMI ≥25 kg/m² and <45 kg/m²
- Weight stable (less than 5% change in the past 6 months)
- Generally healthy individuals
- Not meeting recommended activity guidelines for aerobic or resistance exercise
- Uncontrolled cardiovascular, metabolic, renal, or pulmonary disease
- Cancer treatment in the past 5 years
- Untreated thyroid disease or other medical conditions affecting weight or energy metabolism
- Current use of weight loss medication or other medications likely to impact energy balance
- Bariatric surgery or extensive bowel resection in the past 2 years
- Current or recent history (past 2 years) of eating disorder
- Diagnosis of insomnia, sleep apnea, or other sleep and circadian disorders
- Non-English speaking
- HbA1c >6.5%
Universiteit van Utah306 actieve klinische studies om te verkennenCentraal Contactpersoon
Contact: Tanya M Halliday, PhD, 801-213-1364, [email protected]
Contact: Study Email Study Email, 8014487897, [email protected]
1 Studielocaties in 1 landen
Utah
University of Utah HPER E Buildling, Salt Lake City, Utah, 84112, United States
Jason V Thomas, MS, Contact, [email protected]
Tanya M Halliday, PhD, Hoofdonderzoeker
Recruterend