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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01529281
Other study ID # Northumbria_How_BCAA
Secondary ID
Status Completed
Phase N/A
First received February 2, 2012
Last updated February 6, 2012
Start date June 2011
Est. completion date September 2011

Study information

Verified date February 2012
Source Northumbria University
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Food Standards Agency
Study type Interventional

Clinical Trial Summary

It is well documented that exercise-induced muscle damage (EIMD) decreases muscle function and causes severe soreness and discomfort. Branched-chain amino acid (BCAA) supplementation has been shown to increase protein synthesis and decrease muscle protein breakdown, however, the effects of BCAAs on recovery from EIMD are unknown. Thus, the aim of this study was to examine the effects of a BCAA supplement on markers of muscle damage.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date September 2011
Est. primary completion date September 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Resistance trained males

Exclusion Criteria:

- Muscular skeletal disorders

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Branch Chain Amino Acid (BCAA)
Supplementation lasted for a total of 12 days; this was based on previous research showing a positive with BCAA supplementation on markers of muscle damage. Participants ingested 10 g, twice per day (morning and evening) of BCAA . The BCAA supplement contained a ratio of 2:1:1 (leucine, isoleucine and valine, respectively). The BCAA was in powder form where each serving was mixed with ~300 ml of water.
Placebo - asparmate
Supplementation lasted for a total of 12 days. Participants ingested an equivalent looking volume to 10 g of BCAA, twice per day (morning and evening) of placebo (aspartame based artificial sweetener). The BCAA supplement contained a ratio of 2:1:1 (leucine, isoleucine and valine, respectively). The artificial sweetener was in powder form where each serving was mixed with ~300 ml of water.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Northumbria University

Outcome

Type Measure Description Time frame Safety issue
Primary Maximal voluntary contraction Isometric MVC of the participants' dominant knee extensors was assessed using a strain gauge. MVCs were performed for 3 s with a 60 s rest between each repetition. pre exercise, 24 h, 48 h, 72 h, 96 h post-exercise No
Secondary Limb girths Mid-thigh and calf circumference was assessed as a measure of limb swelling using an anthropometric tape measure. Both measures were obtained with the participant in a standing position. pre-exercise, 24h, 48h, 72h, 96h No
Secondary Vertical jump Vertical jump (VJ) performance was assessed using the Vertec instrument. Participants performed a counter movement jump. pre-exercise, 24h, 48h, 72h, 96h No
Secondary Creatine kinase Plasma CK was determined from an earlobe capillary blood sample. The sample (30 microlitres) was analysed immediately using an automated, dry slide photospectrometer. pre-exercise, 24h, 48h, 72h, 96h No
Secondary Muscle soreness Muscle soreness - Participants were asked to perform and hold a squat (90° knee angle) whilst they rated their perceived muscle soreness on a 200 mm visual analogue scale. The scale consisted of a line from 0 mm (no pain) to 200 mm (unbearably painful). pre-exercise, 24h, 48h, 72h, 96h No
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