A Clinical Study to Investigate the Effects of Creatine Supplementation on Muscle Energetics and Cognitive Function in Young Healthy Male Athletes and an Ageing Population
Study Details
Study Description
Brief Summary
This study will examine the impact of creatine supplementation on muscle function and cognitive performance in young and older subjects.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
This is a randomised, double-blind study of the effects of creatine supplementation on muscle energetics and cognitive function, using 31P-MRS and fMRI. 31P-MRS data will be acquired continuously during exercise phase and in the post-exercise metabolic recovery phase. Participants will undergo a fMRI scan of the brain to record changes in the blood oxygen level dependent (BOLD) signal during a series of cognitive tests. In addition, participants will undergo a resting state BOLD scan and a structural MRI scan for localization of brain regions.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Creatine Group Whey protein (30 g) and creatine supplement (5 g) shaken with 250-300 ml water in a blender bottle, and the full shake to be taken twice a day for 14 days. |
Drug: Creatine
Creatine powder (5 g)
|
| Placebo Comparator: Placebo Group Whey protein (30 g) and bulking agent powder (5 g) shaken with 250-300 ml water in a blender bottle, and the full shake to be taken twice a day for 14 days. |
Drug: Placebo
Bulking agent powder (5 g)
|
Outcome Measures
Primary Outcome Measures
- PCr Concentration (at rest) [Baseline to Day 3, 7 and 14]
Change in PCr concentration (at rest), as measured by 31P- MRS on the calf. Static MRS will be acquired at rest up to 2 min.
Secondary Outcome Measures
- PCr concentration during recovery [Baseline to Day 3, 7, and 14]
Change in PCr concentration (during recovery) as measured by 31P- MRS on the calf. Dynamic MRS will be acquired with the patient at rest for up to 20 min.
- Change in PCr from rest to recovery [Baseline to Day 3, 7, and 14]
Change in PCr concentration (from rest to recovery) as measured by 31P- MRS on the calf.
- PCr recovery rate (PCr(T1/2)) [Baseline to Day 3, 7 and 14]
Measured by 31P-MRS on the leg
- ADP recovery rate (ADP (T1/2)) [Baseline to Day 3, 7 and 14]
Measured by 31P-MRS on the leg
- pH at the end of pedal test, or at the time of voluntary cessation (Post-pedal test pH) [Baseline to Day 3, 7 and 14]
Measured by 31P-MRS on the leg
- Lowest pH measured during pedal test or recovery (Minimum pH) [Baseline to Day 3, 7 and 14]
Measured by 31P-MRS on the leg
- BOLD signal in the brain [Baseline to Day 14]
Change in BOLD signal, as measured by an fMRI scan of the brain. Data may be examined at both a whole-brain and region of interest (ROI) level, with ROIs defined either anatomically or based on clusters derived from the group data.
- Cognitive function [Baseline to Day 14]
A standard test battery will be used to examine changes in behavioural measures of cognition, including speed of processing (detection task), attention/vigilance (identification task), working memory, visual learning and memory, and reasoning and problem solving. In addition, a visual analogue scales (VAS) will be used to assess subjective mood state.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Healthy volunteer: Group 1: male; Group 2: male or female.
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Aged 18-35 years (Group 1), or 50-70 years (Group 2).
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Dietary protein intake at or near the current recommended daily amount (0.75 to 0.85 g protein/kg/day).
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Participation in regular physical activity (aerobic and resistance training) 2-3 times a week for at least 6 months before the study starts (Group 1 only).
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Willingness to maintain a stable lifestyle throughout the study.
Exclusion Criteria:
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Clinically relevant abnormal history, physical findings, ECG, or laboratory values at the pre-trial screening assessment that could interfere with the objectives of the trial or the safety of the volunteer.
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Presence of acute or chronic illness or history of chronic illness sufficient to invalidate the volunteer's participation in the trial or make it unnecessarily hazardous.
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Impaired endocrine, thyroid, hepatic, respiratory, neurological, or renal function, diabetes mellitus, cardiovascular disease, coagulation disorder, autoimmune disease, phenylketonuria, hyperlipidaemia, or history of any psychotic mental illness.
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Any impairment affecting mobility and muscle metabolism of the lower limbs (such as arthritis).
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Surgery (eg stomach bypass) or medical condition that might affect absorption of supplements.
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Inability to complete the structured exercise program.
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Blood pressure and heart rate in seated position at the screening examination outside the ranges 90-140 mm Hg systolic, 40-90 mm Hg diastolic; heart rate 35-100 beats/min (Group 1) or 40-100 beats/min (Group 2).
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Metal implants that may affect the MRI scan, eg gold tooth or other metal dental devices (normal dental fillings are allowed), pacemaker, mechanical heart valve, replacement joint, shrapnel. If any metal in the body is identified, the investigators will make a decision, as to whether the subject should participate in the study.
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History of claustrophobia or subject feels unable to lie still on their back for a period of 90 mins in the MRI scanner, or subject unable to perform the required muscle exercise in the MRI scanner.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | GSK Investigational Site | London | United Kingdom | NW10 7EW |
Sponsors and Collaborators
- GlaxoSmithKline
Investigators
- Study Director: GSK Clinical Trials, GlaxoSmithKline
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 201131
- RH02061