Effects of Carbohydrates Versus Carbohydrates + Protein on Resistance Training Outcomes (CHO & PRO+CHO)

May 15, 2026 updated by: Michael Roberts, Auburn University

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

Completed

Study Type

Interventional

Enrollment (Actual)

25

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Alabama
      • Auburn, Alabama, United States, 36879-5432
        • School of Kinesiology

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • Whey protein + CHO
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:
  • Whey protein only
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:
  • Whey protein + CHO
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:
  • Whey protein only

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 12, 2025

Primary Completion (Actual)

September 15, 2025

Study Completion (Actual)

September 16, 2025

Study Registration Dates

First Submitted

May 15, 2026

First Submitted That Met QC Criteria

May 15, 2026

First Posted (Actual)

May 20, 2026

Study Record Updates

Last Update Posted (Actual)

May 20, 2026

Last Update Submitted That Met QC Criteria

May 15, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified individual participant data are publicly available via the Open Science Framework

IPD Sharing Time Frame

Data are already available

IPD Sharing Access Criteria

Publicly available with no access restrictions

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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