- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01489930
Effects of Resistance and Endurance Training on Synthesis of Individual Muscle Proteins in Young and Older Adults
Loss of skeletal muscle strength and skeletal muscle mass occurs with of aging. This are-related decline in skeletal muscle mass and skeletal muscle strength is a major underlying factor contributing to many of the metabolic disorders and frailty of the investigators rapidly expanding aging population. Endurance (aerobic) and resistance exercise training programs have been shown to effectively reverse the age-related decline in metabolic and contractile muscle functions. The investigators will measure synthesis rates of individual muscle proteins in 36 each of young (18-30 yrs) and 36 older (> 65 yrs) people to determine their response to 8 weeks each of endurance, resistance, combined endurance and resistance training, or placebo exercise training.
Hypotheses.
- to measure fractional synthesis rates of multiple muscle proteins and identify those that are enhanced by an endurance exercise program
- to determine whether changes in protein synthesis in response to endurance exercise programs are dependent on age
- to measure fractional muscle synthesis rates of multiple muscle proteins and to identify those that are enhanced by a resistance exercise program
- to determine whether changes in protein synthesis in response to resistance exercise programs are dependent on age
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minnesota
-
Rochester, Minnesota, United States, 55905
- Mayo Clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy
- 18 to 30 or >65 years
- Males and Females
Exclusion Criteria:
- Regular Exercise Program
- Smoking
- Cardiometabolic Disease (diabetes, cardiovascular disease, thyroid disorders)
- Drugs known to impair metabolic function (beta blockers, steroids)
- Allergies to lidocaine
- Physical disability that precludes exercise
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Endurance Exercise
Participants will perform 8-weeks of moderate intensity endurance (cycling) exercise
|
Participants will perform 8-weeks of endurance exercise training.
Participants will train 5 days per week for 60 min at 65% of VO2 peak.
|
|
Experimental: Resistance Exercise
Participants will perform 8-weeks of whole-body resistance exercise training.
|
Participants will perform 8-weeks of resistance exercise training.
Participants will train 4 days per week for ~60 min.
Two days will focus on lower body resistance training and two days will focus on upper body.
|
|
Experimental: Control / Combined Training
Participants will perform 8-weeks of no exercise, followed by an additional 8-weeks of combined endurance plus resistance exercise training.
|
Participants will perform 8-weeks of no exercise (control), followed by 8-weeks of combined endurance and resistance training.
Participants will endurance train 5 days per week for 30 min at 65% of VO2 peak and resistance train 4 days per week for 30 min.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Skeletal Muscle Protein Synthesis
Time Frame: Measured at week 0 (baseline) and week 8
|
The investigators will determine the change from baseline in skeletal muscle protein synthesis.
Measurments will be performed at baseline and following 8 weeks of exercise training.
|
Measured at week 0 (baseline) and week 8
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mitochondrial Function
Time Frame: Measured at week 0 (baseline) and week 8
|
The investigators will determine the change from baseline in mitochondrial function.
Measurments will be performed at baseline and following 8 weeks of exercise training.
|
Measured at week 0 (baseline) and week 8
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: K. Sreekumaran Nair, MD, PD, Mayo Clinic
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 07-007689
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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