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Acute Study on Muscle Soreness, Damage, and Performance

2020-01-22 12:12:55 | BioPortfolio

Summary

The acute study will evaluate pre- and post-exercise ingestion of a multi-ingredient supplement in a randomized, double-blind, placebo-controlled, crossover design. Participants will complete one enrollment visit, in which they will sign a consent form and complete a health history questionnaire. Participants will complete two interventions, with three visits each (6 visits total), in which a treatment beverage (pre/post supplement, or non-caloric placebo) will be consumed within 30 minutes prior to exercise and within 15 minutes post-exercise, in random order. Total time from enrollment to completion will be at least 14 days. Testing visits will be separated by a minimum of 7 days of rest to allow for recovery and washout, based on a half-life of ≤8 hours for all ingredients present in the supplement.

Study Design

Conditions

Soreness, Muscle

Intervention

Pre-workout plus and protein recovery plus, Placebo

Location

University of North Carolina at Chapel Hill
Chapel Hill
North Carolina
United States
27599

Status

Recruiting

Source

Pharmanex

Results (where available)

View Results

Links

Published on BioPortfolio: 2020-01-22T12:12:55-0500

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