Clinical Trials Directory

Trials / Completed

CompletedNCT04230824

Chronic Study on Body Composition, Training, Performance, and Recovery

A Randomized, Double-blind, Placebo Controlled, Single-center Study to Determine the Effects of Pre-workout and Recovery Formulations on Soreness, Performance, Tolerance and Safety Outcomes in Healthy Adults Undergoing Training Program

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
69 (actual)
Sponsor
Pharmanex · Industry
Sex
All
Age
25 Years – 50 Years
Healthy volunteers
Accepted

Summary

The chronic phase of the study will evaluate the effects of pre-exercise and post-exercise ingestion of a multi-ingredient supplement on adaptations to a 6-week exercise program consisting of both resistance training and high intensity aerobic exercise, using a randomized, double-blind, placebo-controlled design. Participants will complete an enrollment/familiarization visit, a baseline testing session, followed by a 6-week supervised exercise intervention, and post-testing session identical to baseline testing. Participants will be randomized during the baseline session to groups receiving either 1) Active Treatment (pre-post supplementation), 2) placebo (noncaloric beverage), or 3) control, not participating in exercise or consuming a treatment. During the supervised 6-week resistance training program, participants will complete a moderate-intensity warm-up, a full-body resistance training workout (2 x per week) and an interval training session (1 x per week). Thirty-minutes prior to each training session, and within 15 minutes post-exercise, participants will consume their randomly assigned treatment beverage. Body composition, blood markers of muscle damage/recovery, strength, and performance tests will be measured before (baseline) and after training (Post) to evaluate the effects of supplementation. All data collection will be conducted by the Principal Investigator and Research Assistants. All subjects will report to the Applied Physiology Laboratory and Human Performance Center in Fetzer Hall for all testing and training sessions, which will span approximately 8 weeks.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPre-workout plus and Protein recovery plusproducts consumed prior and after exercise
OTHERPlaceboplacebo product consumed prior and after exercise
OTHER6-week resistance training programparticipants will complete a moderate-intensity warm-up, a full-body resistance training workout (2 x per week) and an interval training session (1 x per week)

Timeline

Start date
2021-02-01
Primary completion
2021-07-01
Completion
2022-01-01
First posted
2020-01-18
Last updated
2022-01-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04230824. Inclusion in this directory is not an endorsement.