- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06606704
Effects of Resistance-band Training and Creatine Supplementation Strategies in Healthy Older Adults
Effects of Resistance-band Training and Creatine Supplementation in Healthy Older Adults
The primary purpose is to compare the effects of creatine supplementation (bolus ingestion of 5 grams vs. 3 grams) during 16 weeks of resistance-band training on measures of body composition (i.e., whole-body lean tissue mass, total body water), arm and leg muscle thickness (growth), muscle performance (i.e., power, strength, endurance) and functional ability (i.e., walking speed, balance).
A secondary purpose of this research is to examine the effects of bolus ingestion of creatine (5 grams) compared to intermittent ingestion of creatine (2 x 2.5 grams) during 16 weeks of resistance-band training on measures of body composition (i.e., whole-body lean tissue mass, total body water), arm and leg muscle thickness (growth), muscle performance (i.e., power, strength, endurance) and functional ability (i.e., walking speed, balance).
Study Overview
Status
Conditions
Detailed Description
Resistance-band training is safe, conveient, easy-to-use, eliminates potential barriers to exercise participation (i.e., lack of transportation to and from commercial training facilities) and results in high exercise compliance and adherence. Further, resistance-band training results in similar improvements in muscle performance and functional ability compared to traditional resistance-type training using free-weights and machines.
Creatine is a naturally occurring nitrogen-containing compound produced in the body in the liver and brain and can also be found in food products such as red meat and seafood or through commercially available manufactured creatine products.
Evidence-based research shows that creatine supplementation, when ingested during a resistance exercise training program, improves measures of lean mass and muscle growth, muscle performance and functional ability. However, the optimal creatine supplementation protocol to achieve these benefits is unknown.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Darren Candow
- Phone Number: 306-585-4906
- Email: Darren.Candow@uregina.ca
Study Locations
-
-
Saskatchewan
-
Regina, Saskatchewan, Canada, S4S4H4
- Recruiting
- University of Regina
-
Contact:
- Darren G Candow, PhD
- Phone Number: 3062090280
- Email: Darren.Candow@uregina.ca
-
Contact:
- Darren G Candow, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- if you are 50 years of age and older
- if you have not been performing more than 1 resistance training session per week for the past 6 weeks or more.
Exclusion Criteria:
- if you have taken creatine supplements within 30 days prior to the start of the study
- if you have pre-existing allergies to the placebo (corn-starch maltodextrin).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Placebo
|
(Serving: 8 grams of placebo in the morning; Servings 2: 8 grams of placebo at least 6 hours after Serving 1).
|
|
Experimental: Creatine Bolus 5
|
(Serving 1: 5 grams of creatine + 3 grams of placebo in the morning; Serving 2: 8 grams of placebo at least 6 hours after Serving 1).
|
|
Experimental: Creatine Bolus 3
|
(Serving 1: 3 grams of creatine + 5 grams of placebo in the morning; Serving 2: 8 grams of placebo at least 6 hours after Serving 1).
|
|
Experimental: Creatine Intermittent 5
|
(Serving 1: 2.5 grams of creatine + 5.5 grams of placebo in the morning, Serving 2: 2.5 grams of creatine + 5.5 grams of placebo at least 6 hours after Serving 1).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Whole-body lean mass (kg)
Time Frame: baseline, week 16
|
Bioelectrical impedance analysis
|
baseline, week 16
|
|
Muscle Hypertrophy (cm)
Time Frame: baseline, week 16
|
B-mode ultrasound
|
baseline, week 16
|
|
Strength (kg)
Time Frame: baseline, week 16
|
1-repetition maximum leg press and chest press
|
baseline, week 16
|
|
Endurance (number of repetitions to fatigue)
Time Frame: baseline, week 16
|
Leg press and chest press
|
baseline, week 16
|
|
Power (feet)
Time Frame: baseline, week 16
|
medicine ball throw
|
baseline, week 16
|
|
Balance (Centre of Pressure)
Time Frame: baseline, week 16
|
Force Plate
|
baseline, week 16
|
|
Gait Speed (meters)
Time Frame: baseline, week 16
|
Walking distance
|
baseline, week 16
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Darren Candow, University of Regina
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 853
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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