Effects of Carbohydrates Versus Carbohydrates + Protein on Resistance Training Outcomes
CHO & PRO+CHO
1 other identifier
interventional
25
1 country
1
Brief Summary
Higher energy and carbohydrate intakes have been hypothesized to enhance resistance training adaptations, yet empirical evidence remains mixed. This study investigated whether supplemental carbohydrate-energy intake improves muscle hypertrophy, strength, and fatigue resistance in resistance-trained men. Twenty resistance-trained men completed a quasi-randomized, double-blinded, counterbalanced crossover trial. Participants consumed either a daily protein-only supplement (30 g protein, 4 g carbohydrate) or a daily protein-plus-carbohydrate supplement (30 g protein, 54 g carbohydrate) for 8 weeks each, followed by crossover, while continuing their habitual training and diet. Primary outcomes included lean mass (dual-energy x-ray absorptiometry), muscle thickness and cross-sectional area (ultrasound), back squat one-repetition maximum, knee extensor peak torque, and fatigue index. The carbohydrate-protein supplement produced significantly higher daily energy and carbohydrate intake compared to the protein-only supplement, with no differences in protein intake, fat intake, or training volume. No significant between-condition differences were observed for any outcome. These results suggest that modest increases in carbohydrate-energy intake outside of an energy deficit are unlikely to meaningfully enhance muscle hypertrophy, strength, or fatigue resistance in trained men.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 12, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 16, 2025
CompletedFirst Submitted
Initial submission to the registry
May 15, 2026
CompletedFirst Posted
Study publicly available on registry
May 20, 2026
CompletedMay 20, 2026
May 1, 2026
4 months
May 15, 2026
May 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Lean mass
Bone-free lean tissue mass according to Dual-energy X-ray absorptiometry (DXA)
Baseline, 8 weeks (mid-point), 16 weeks (post)
Mid-thigh muscle thickness
Change in lateral thigh muscle thickness (vastus lateralis and vastus intermedius)
Baseline, 8 weeks (mid-point), 16 weeks (post)
Back Squat One-Repetition Maximum
Change in back squat 1RM
Baseline, 8 weeks (mid-point), 16 weeks (post)
Knee Extensor Peak Torque
Change in knee extensor peak torque using isokinetic dynamometry
Baseline, 8 weeks (mid-point), 16 weeks (post)
Study Arms (2)
CHO
EXPERIMENTALDaily consumption of a whey protein and maltodextrin mixture providing 30 g protein, 54 g carbohydrate, and 2 g fat per 92 g serving for 8 weeks.
PRO
ACTIVE COMPARATORDaily consumption of a whey protein blend providing 30 g protein, 4 g carbohydrate, and 2 g fat per 39 g serving for 8 weeks.
Interventions
Daily consumption of a whey protein and maltodextrin mixture providing 30 g protein, 54 g carbohydrate, and 2 g fat per 92 g serving for 8 weeks
Daily consumption of a whey protein blend providing 30 g protein, 4 g carbohydrate, and 2 g fat per 39 g serving for 8 weeks.
Eligibility Criteria
You may qualify if:
- Male sex
- Aged 18-40 years
- BMI not exceeding 35 kg/m²
- Minimum of two years resistance training experience
- Resistance training frequency of at least four days per week
- No known allergy to whey protein supplements
You may not qualify if:
- Known cardio-metabolic disease (e.g., clinical obesity, diabetes, hypertension, heart disease)
- Any condition contraindicating participation in resistance training
- Known allergy to whey protein supplements
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
School of Kinesiology
Auburn, Alabama, 36879-5432, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Masking Details
- Participants were blinded (supplements were provided in clear, unlabeled containers). Assessors/testers were blinded to group allocation. The ultrasound technician was blinded.
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
May 15, 2026
First Posted
May 20, 2026
Study Start
May 12, 2025
Primary Completion
September 15, 2025
Study Completion
September 16, 2025
Last Updated
May 20, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- Data are already available
- Access Criteria
- Publicly available with no access restrictions
De-identified individual participant data are publicly available via the Open Science Framework