Creatine Timing and Resistance Training Adaptations.
The Effect of Creatine Timing on Resistance Training Adaptations: A Within-subject Design
1 other identifier
interventional
10
1 country
1
Brief Summary
Emerging evidence suggests that the timing of creatine supplementation may be an important regulator of muscle growth and strength. It is unclear whether creatine ingested before or after resistance training is more beneficial. A limitation of previous research is the use of a between subject design. A between subject design is associated with several potential confounders (habitual diet, genetics, activities of daily living, etc.) that may have masked the true effect. The purpose of this study is to examine the effect of creatine timing (creatine before vs. creatine after) using a randomized, double blind, repeated measures, within-subject design. Participants will resistance train their left arm and left leg one day and their right arm and right leg the next day. Participants will supplement with creatine BEFORE one of the training days (randomized to either left or right side) and on the opposite training day (opposite side of the body to the previous training day) supplement with creatine AFTER training. Having the same person in both conditions will control for genetics, habitual diet, other daily activities, and so on, that may have confounded previous research. Muscle mass and strength changes will be measured in each limb prior to and following 8 weeks of training to determine whether creatine timing influenced muscle growth. Research Question: To determine whether creatine supplementation timing (i.e., before versus after training) effects 8 weeks of resistance training adaptations (i.e., muscle growth and strength changes).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable healthy
Started Sep 2018
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 15, 2018
CompletedFirst Submitted
Initial submission to the registry
September 18, 2018
CompletedFirst Posted
Study publicly available on registry
September 20, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2020
CompletedDecember 16, 2020
December 1, 2020
1.7 years
September 18, 2018
December 11, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Hypertrophy (Muscle thickness will be determined via ultrasound)
Muscle thickness will be determined via ultrasound.
8 weeks
Strength (1 repetition maximum will be determined via standard 1RM protocols)
1 repetition maximum will be determined via standard 1RM protocols
8 weeks
Study Arms (2)
Creatine Before
EXPERIMENTALReceives Creatine before and placebo after training.
Creatine After
EXPERIMENTALReceives creatine after and placebo before training.
Interventions
Participants will resistance train their left arm and left leg one day and their right arm and right leg the next day. Participants will supplement with creatine BEFORE one of the training days (randomized to either left or right side) and on the opposite training day (opposite side of the body to the previous training day) supplement with creatine AFTER training. Having the same person in both conditions will control for genetics, habitual diet, other daily activities, and so on, that may have confounded previous research. Muscle mass and strength changes will be measured in each limb prior to and following 8 weeks of training to determine whether creatine timing influenced muscle growth. Research Question: To determine whether creatine supplementation timing (i.e., before versus after training) effects 8 weeks of resistance training adaptations (i.e., muscle growth and strength changes).
Eligibility Criteria
You may qualify if:
- You may be able to participate in this study if you are between the ages of 18 and 35, are free of disease (e.g., diabetes), do not currently take creatine or other supplements (within the last 12 weeks), and have no known cardiovascular disease or other medical conditions which prevent you from performing physical activity or this type of nutritional supplement.
- You must also have no other reasons that might make exercise unsafe for you. You will complete a questionnaire (Get Active Questionnaire) to help identify any illness or health concern that could be worsened by performing exercise or make exercise unsafe for you.
You may not qualify if:
- You will not be eligible to participate in this study:
- If your doctor has informed you that you have a heart condition and should only do physical activity recommended by a doctor.
- If you feel pain in your chest when you perform any physical activity.
- If in the past the month you have had chest pain when you were not doing any physical activity.
- If you lose your balance or consciousness because of dizziness.
- If you have bone or joint problem (for example, back, knee, or hip) that could be made worse by a change in your physical activity.
- You have previously had a heart attack or stroke
- If you know of any other reason why you should not do physical activity.
- You currently take creatine supplements and/or other "performance enhancing" nutritional supplements
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Brandon University
Brandon, Manitoba, R7A 6A9, Canada
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Scott C Forbes, PhD
Brandon University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- An independent researcher will label the placebo and creatine and only reveal which group is which after data has been analyzed.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 18, 2018
First Posted
September 20, 2018
Study Start
September 15, 2018
Primary Completion
June 1, 2020
Study Completion
June 1, 2020
Last Updated
December 16, 2020
Record last verified: 2020-12
Data Sharing
- IPD Sharing
- Will not share