Skip to content

Dileucine and Resistance Training Adaptations

A Pilot Study to Examine Changes in Resistance Training Adaptations After Leucine and Dileucine Ingestion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06121869
Acronym
DTS
Enrollment
34
Registered
2023-11-08
Start date
2021-05-07
Completion date
2023-06-29
Last updated
2023-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertrophy, Strength Training Adaptations, Weight-Bearing Strengthening Program

Keywords

Peptides, Dipeptide, Adaptations, Exercise, Dietary Supplements

Brief summary

This study seeks to compare the observed changes in resistance training adaptations after supplementation of isomolar amounts of leucine or dileucine in healthy resistance-trained men. This will provide a better understanding of supplementation with leucine versus dileucine over a 10-week period in regards to increasing muscular performance.

Detailed description

The study will be conducted using a randomized, double-blind approach with individuals being provided daily 2-gram doses of leucine, 2-gram doses of dileucine, or a placebo. Daily blinded supplementation will occur each day for a 10-week period of time while completing a heavy resistance training program. Participants follow the resistance training program for a total of 10 weeks. To compare the efficacy of leucine in form of amino acid or dipeptide supplementation on resistance training adaptations, changes in fat-free, lean, and fat mass will be determined using a 4-compartment body composition model. Skeletal muscle cross-sectional area will be assessed using ultrasound. Maximal strength, muscular endurance, and power will also be assessed. Participants will be required to provide weekly compliance and complete one supervised workout per week. After 2, 6, and 10 weeks of following the supplementation and resistance training regimens, participants will return to the laboratory to complete testing bouts consisting of identical assessments of body composition, muscular strength, muscular endurance, lower-body power, and anaerobic capacity. Adverse events related to each supplementation group will be recorded and assessed.

Interventions

DIETARY_SUPPLEMENTPlacebo

Participants will supplement daily for 10 weeks with 2 grams rice flower placebo in capsule form. On training days, participants will consume their assigned supplement within 60 minutes of completing their workout. On non-training days, participants will consume their assigned supplement with their first meal of the day. All doses will be consumed with 8-12 ounces of water.

DIETARY_SUPPLEMENTLeucine

Participants will supplement daily for 10 weeks with 2 grams leucine in capsule form. On training days, participants will consume their assigned supplement within 60 minutes of completing their workout. On non-training days, participants will consume their assigned supplement with their first meal of the day. All doses will be consumed with 8-12 ounces of water.

DIETARY_SUPPLEMENTDileucine

Participants will supplement daily for 10 weeks with 2 grams dileucine (RAMPS, Ingenious Ingredients, TX, USA) in capsule form. On training days, participants will consume their assigned supplement within 60 minutes of completing their workout. On non-training days, participants will consume their assigned supplement with their first meal of the day. All doses will be consumed with 8-12 ounces of water.

Sponsors

Ingenious Ingredients, L.P.
CollaboratorUNKNOWN
Lindenwood University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Masking description

All supplements will be provided in blinded, labeled containers prior to them arriving to the site. Each supplement will be of similar volume, texture, and labeled in indistinguishable bottles to ensure blinding of both participant and invesitigator

Intervention model description

Randomized, Double-Blind, Placebo-Controlled

Eligibility

Sex/Gender
MALE
Age
18 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* Male * Between the ages of 18-39 years of age * Currently participating in resistance training exercise

Exclusion criteria

* Female * Participants who are determined to not be weight stable defined as week 0 and week 2 body mass levels deviating by 3% or more. * Any individual who is currently being treated for or diagnosed with a cardiac, respiratory, circulatory, musculoskeletal, metabolic, immune, autoimmune, psychiatric, hematological, neurological or endocrinological disorder or disease. * Body mass index \> 25 kg/m2. Individuals with a body mass index greater than 25 kg/m2, but a body fat percentage less than 25% fat will be accepted into the study * Individuals who present with any previous injury or illness that would prevent them from appropriately completing all exercise lifts. * Participants who are not able to fit onto the DEXA table will not be able to participate in the research due to size restrictions of the equipment. This typically includes individuals exceeding 400 pounds or those greater than 6'4. * Those individuals with less than 12 months of structured resistance training experience will be excluded from the study. * Individuals whose maximal relative upper body strength is below 1.0 will be excluded. * Individuals whose maximal relative lower body strength is below 1.5 will be excluded. * All participants who DO NOT abstain from taking any additional forms of nutritional supplementation deemed to be ergogenic or that will impact resistance training adaptations (pre-workouts, creatine, beta-alanine, etc.) for four weeks prior to beginning this study and for the entire duration of the study. * Individuals who are currently using or have used within the past 12 months anabolic-androgenic steroids.

Design outcomes

Primary

MeasureTime frameDescription
Fat-Free Mass10 weeksFat-free mass will be determined via Dual-Energy X-Ray Absorptiometry
Leg Press 1RM10 weeksLeg Press 1RM will be measured using the leg press (lower-body) exercise.
Bench Press 1RM10 weeksBench Press 1RM will be measured using the bench press (upper-body) exercise.
Maximal Isometric Mid-Thigh Pull Force Production10 weeksMaximal Isometric Mid-Thigh Pull Force Production will be measured using an isometric mid-thigh pull test

Secondary

MeasureTime frameDescription
Extracellular Body Water10 weeksExtracellular Body Water will be determined via bioelectrical impedance analysis
Intracellular Body Water10 weeksIntracellular Body Water will be determined via bioelectrical impedance analysis
Skeletal muscle cross-sectional area10 weeksSkeletal muscle cross-sectional area will be measured using ultrasound measurements of the participants thigh muscles.
Bench Press Repetitions to Fatigue10 weeksBench Press repetitions to fatigue will be measured using the bench press (upper-body) exercises on four separate occasions (visits 2, 3, 4, and 5). To complete this assessment, study participants will use a load that corresponds to 80% of their Visit 2 1RM for bench press exercise and will be instructed to complete as many repetitions as they can until failure for one set of each exercise. Failure will be defined as resting for more than two seconds throughout any point on the exercise set or technique failure.
Fat Mass10 weeksFat mass will be determined via Dual-Energy X-Ray Absorptiometry
Peak Anaerobic Power10 weeksPeak Anaerobic Power will be measured using a Wingate Anaerobic Test lasting 30-seconds at a load set to 7.5% of week 0 body mass
Mean Anaerobic Power10 weeksMean Anaerobic Power will be measured using a Wingate Anaerobic Test lasting 30-seconds at a load set to 7.5% of week 0 body mass
Rate of Fatigue10 weeksRate of Fatigue will be measured using a Wingate Anaerobic Test lasting 30-seconds at a load set to 7.5% of week 0 body mass
Maximal Concentric Rate of Force Development10 weeksMaximal concentric rate of force development will be measured using a countermovement jump performed on a force plate
Leg Press Repetitions to Fatigue10 weeksLeg Press repetitions to fatigue will be measured using the leg press (lower-body) exercises on four separate occasions (visits 2, 3, 4, and 5). To complete this assessment, study participants will use a load that corresponds to 80% of their Visit 2 1RM for leg press exercise and will be instructed to complete as many repetitions as they can until failure for one set of each exercise. Failure will be defined as resting for more than two seconds throughout any point on the exercise set or technique failure.
Lean mass10 weeksLean mass will be determined via Dual-Energy X-Ray Absorptiometry
% Body Fat10 weeks% Body Fat will be determined via Dual-Energy X-Ray Absorptiometry
Total body water10 weeksTotal Body Water will be determined via bioelectrical impedance analysis

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026