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NCT05544955 · ClinicalTrials.gov registry record · NA

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

A NA study of Physical Performance and Hypertrophy, sponsored by Marymount University.

Completed
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT05544955: Completed NA study of Physical Performance and Hypertrophy, sponsored by Marymount University.

NCT05544955 is a NA study of Physical Performance and Hypertrophy that has completed, run by Marymount University. The registered enrollment target is 40 participants, below the 3,603-participant average among 6 other Physical Performance trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05544955, a NA study of Physical Performance and Hypertrophy, has completed, sponsored by Marymount University.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

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

Primary Outcome

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

Interventions

  • 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

Study Locations (1)

Virginia

  • Marymount University - Arlington

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2022-09-17
Est. Completion 2022-12-31
Phase NA
Marymount University

6 total trials

What the finished NCT05544955 record still lists

NCT05544955 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 3,603-participant average among 6 other Physical Performance trials with a reported enrollment target (99% lower).

The record links to 2 conditions, with Physical Performance appearing as the primary indexed condition, and to 2 interventions - of which isolate whey protein prior to and immediately after resistance training is the first listed.

NCT05544955 reports a single indexed study location in Virginia.

Frequently Asked Questions

What is clinical trial NCT05544955 about?

NCT05544955 is a clinical study titled "Protein Ingestion Timing on Body Composition and Biochemical Markers in Resistance-trained Males". Protein ingestion timing is an important component for muscle accretion. The investigators hypothesized that protein ingestion timing could affect muscular adaptations and performance in resistance-trained men.

What is the current status of trial NCT05544955?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2022-09-17. Estimated completion is 2022-12-31.

What conditions does trial NCT05544955 study?

This clinical trial studies the following conditions: Physical Performance, Hypertrophy.

What interventions are being tested in trial NCT05544955?

The interventions under investigation include: 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 (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT05544955?

This trial is sponsored by Marymount University, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05544955 being conducted?

This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05544955, the US trial registry maintained by the National Library of Medicine. NCT05544955 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.