- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07600138
Effects of Carbohydrates Versus Carbohydrates + Protein on Resistance Training Outcomes (CHO & PRO+CHO)
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Alabama
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Auburn, Alabama, United States, 36879-5432
- School of Kinesiology
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: CHO
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 and maltodextrin mixture providing 30 g protein, 54 g carbohydrate, and 2 g fat per 92 g serving for 8 weeks
Other Names:
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.
Other Names:
|
|
Active Comparator: PRO
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.
|
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
Other Names:
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.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lean mass
Time Frame: Baseline, 8 weeks (mid-point), 16 weeks (post)
|
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
Time Frame: Baseline, 8 weeks (mid-point), 16 weeks (post)
|
Change in lateral thigh muscle thickness (vastus lateralis and vastus intermedius)
|
Baseline, 8 weeks (mid-point), 16 weeks (post)
|
|
Back Squat One-Repetition Maximum
Time Frame: Baseline, 8 weeks (mid-point), 16 weeks (post)
|
Change in back squat 1RM
|
Baseline, 8 weeks (mid-point), 16 weeks (post)
|
|
Knee Extensor Peak Torque
Time Frame: Baseline, 8 weeks (mid-point), 16 weeks (post)
|
Change in knee extensor peak torque using isokinetic dynamometry
|
Baseline, 8 weeks (mid-point), 16 weeks (post)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00000295
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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