Exercise-induced Muscle Damage is Reduced in Resistance Trained Athletes by Branch Chain Amino Acids
This study has been completed.
Sponsor:
Northumbria University
Information provided by (Responsible Party):
Northumbria University
ClinicalTrials.gov Identifier:
NCT01529281
First received: February 2, 2012
Last updated: February 6, 2012
Last verified: February 2012
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Exercise-induced Muscle Damage |
Dietary Supplement: Branch Chain Amino Acid (BCAA) Dietary Supplement: Placebo - asparmate |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | Exercise-induced Muscle Damage is Reduced in Resistance Trained Athletes by Branch Chain Amino Acids |
Resource links provided by NLM:
Further study details as provided by Northumbria University:
Primary Outcome Measures:
- Maximal voluntary contraction [ Time Frame: pre exercise, 24 h, 48 h, 72 h, 96 h post-exercise ] [ Designated as safety issue: No ]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.
Secondary Outcome Measures:
- Limb girths [ Time Frame: pre-exercise, 24h, 48h, 72h, 96h ] [ Designated as safety issue: No ]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.
- Vertical jump [ Time Frame: pre-exercise, 24h, 48h, 72h, 96h ] [ Designated as safety issue: No ]Vertical jump (VJ) performance was assessed using the Vertec instrument. Participants performed a counter movement jump.
- Creatine kinase [ Time Frame: pre-exercise, 24h, 48h, 72h, 96h ] [ Designated as safety issue: No ]Plasma CK was determined from an earlobe capillary blood sample. The sample (30 microlitres) was analysed immediately using an automated, dry slide photospectrometer.
- Muscle soreness [ Time Frame: pre-exercise, 24h, 48h, 72h, 96h ] [ Designated as safety issue: No ]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).
| Enrollment: | 12 |
| Study Start Date: | June 2011 |
| Study Completion Date: | September 2011 |
| Primary Completion Date: | September 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: BCAA
Branched chain amino acid
|
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 Comparator: Asparmate
Placebo control containing no protein or carbohydrate
|
Dietary Supplement: 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.
|
Eligibility| Ages Eligible for Study: | 18 Years to 30 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Resistance trained males
Exclusion Criteria:
- Muscular skeletal disorders
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Northumbria University |
| ClinicalTrials.gov Identifier: | NCT01529281 History of Changes |
| Other Study ID Numbers: | Northumbria_How_BCAA |
| Study First Received: | February 2, 2012 |
| Last Updated: | February 6, 2012 |
| Health Authority: | United Kingdom: Food Standards Agency |
ClinicalTrials.gov processed this record on June 18, 2013