Clinical TrialID 8274

Dileucine and Resistance Training Adaptations

NCT06121869

Hypertrophy|Strength Training Adaptations|Weight-Bearing Strengthening Program

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Trial: 1Ingredient: 1Links: 1
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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
8274
Evidence Id
8274
Core Evidence Id
8274
Source Clinical Trial Id
8272
Herb2 Clinical Trial Id
HBCT008272
Nct Id
NCT06121869
Title
Dileucine and Resistance Training Adaptations
Status
Completed
Phase
Study Result
No
Study Condition
Hypertrophy|Strength Training Adaptations|Weight-Bearing Strengthening Program
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: OTHER
Intervention
DIETARY_SUPPLEMENT: Placebo|DIETARY_SUPPLEMENT: Leucine|DIETARY_SUPPLEMENT: Dileucine
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Other
Gender
Male
Age
Adult
Enrollment
34
Outcome Measure
Fat-Free Mass, Fat-free mass will be determined via Dual-Energy X-Ray Absorptiometry, 10 weeks|Leg Press 1RM, Leg Press 1RM will be measured using the leg press (lower-body) exercise., 10 weeks|Bench Press 1RM, Bench Press 1RM will be measured using the bench press (upper-body) exercise., 10 weeks|Maximal Isometric Mid-Thigh Pull Force Production, Maximal Isometric Mid-Thigh Pull Force Production will be measured using an isometric mid-thigh pull test, 10 weeks
Sponsor Collaborator
Lindenwood University|Ingenious Ingredients, L.P.
Funded By
OTHER
Location
Exercise and Performance Nutrition Laboratory, Saint Charles, Missouri, 63301, United States
Other Id
IRB-41-64
Start Date
2021-05-07
Primary Completion Date
2023-06-29
Completion Date
2023-06-29
First Posted
2023-11-08
Results First Posted
Last Update Posted
2023-11-08
Study Document
Study Url
https://clinicaltrials.gov/study/NCT06121869
Title Cn
Title En
Dileucine and Resistance Training Adaptations
Bilingual Status
semi_complete