Protein Ingestion Timing on Body Composition and Biochemical Markers in Resistance-trained Males

Sponsor
Marymount University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05544955
Collaborator
Shahid Beheshti University of Medical Sciences (Other)
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Study Details

Study Description

Brief Summary

Protein ingestion timing is an important component for muscle accretion. We hypothesized that protein ingestion timing could affect muscular adaptations and performance in resistance-trained men.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: isolate whey protein prior to and immediately after resistance training
  • Dietary Supplement: isolate whey protein 3 hours prior to and 3 hours after resistance training
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Basic Science
Official Title:
Comparison of Protein Ingestion Timing on Body Composition, Physical Performance, and Biochemical Markers in Resistance-trained Males
Anticipated Study Start Date :
Sep 17, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Protein ingestion immediately prior to and immediately after resistance training

This arm involved protein ingestion immediately prior to and immediately after resistance training for 12 weeks. Participants will consume 40 g of isolate whey protein at their recommended timing.

Dietary Supplement: isolate whey protein prior to and immediately after resistance training
This arm involved protein ingestion immediately prior to and immediately after resistance training for 12 weeks. Participants will consume 40 g of isolate whey protein at their recommended timing.

Experimental: Protein ingestion 3 hours prior to and 3 hours after resistance training

This arm involved protein ingestion 3 hours prior to and 3 hours after resistance training for 12 weeks. Participants will consume 40 g of isolate whey protein at their recommended timing.

Dietary Supplement: isolate whey protein 3 hours prior to and 3 hours after resistance training
This arm involved protein ingestion 3 hours prior to and 3 hours after resistance training for 12 weeks. Participants will consume 40 g of isolate whey protein at their recommended timing.

Outcome Measures

Primary Outcome Measures

  1. Body Composition [12 weeks]

    Total Lean mass, fat mass, and estimated VAT (g) will be assessed using whole-body DXA

Secondary Outcome Measures

  1. Muscular Strength [12 weeks]

    Using 1 repetition maximum

  2. Muscular Endurance [12 weeks]

    Using leg- and chest press exercises at 75% of the 1-RM

  3. Jump testing [12 weeks]

    Using the vertical and broad jump tests

  4. Pull-ups [12 weeks]

    Using the pull-up test

  5. Liver enzymes (ALT, AST, and GGT) [12 weeks]

    Using Fasting blood samples

  6. Creatinine and Urea Nitrogen [12 weeks]

    Urine samples will be collected using standard procedures

  7. Cholesterol Levels [12 weeks]

    Using Fasting blood samples

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • performing resistance training at least three times a week for 1 year prior to the start of the study

  • not taking any steroids or any illegal agents known to increase muscle size for at least 1 year prior to the start of the study

  • no known medical issues

  • sleeping for at least seven to eight hours during the 24-hour day

Exclusion Criteria:
  • non-willingness to continue protein ingestion or exercise protocols

  • participation in exercise other than the prescribed resistance training program

  • consumption of dietary supplement (other than the protein intervention) during the study period

  • Missing more than one resistance training session or protein ingestion throughout the study period

Contacts and Locations

Locations

Site City State Country Postal Code
1 Marymount University Arlington Virginia United States 22207

Sponsors and Collaborators

  • Marymount University
  • Shahid Beheshti University of Medical Sciences

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Alexei Wong, Associate Professor, Marymount University
ClinicalTrials.gov Identifier:
NCT05544955
Other Study ID Numbers:
  • IR.SBMU.MSP.REC.1400. 708
First Posted:
Sep 19, 2022
Last Update Posted:
Sep 19, 2022
Last Verified:
Sep 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 19, 2022