Structural and Metabolic Determinants of Sarcopenia and the Efficacy of Concentric vs. Eccentric Exercise Training

October 27, 2017 updated by: University of Nottingham

Structural and Metabolic Determinants of Sarcopenia and the Efficacy of Concentric vs. Eccentric Exercise Training: a Novel Temporospatial Approach

The first goal of this study is the follow young and older people over a period of 8 weeks to define the processes responsible for loss of muscle length and width in age-related muscle wasting (sarcopenia) and allow us to look at age-related differences in tendon. Secondly, we will assess two different exercise interventions for reversing human sarcopenia; one which involves shortening of the muscle and the other which involves lengthening, whilst also studying why these exercises work the way they do. This project will have significant implications for our understanding of the control of skeletal muscle and tendon size in humans, particularly in relation to sarcopenia and the surrounding health issues.

Study Overview

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Derbyshire
      • Derby, Derbyshire, United Kingdom, DE22 3DT
        • University of Nottingham

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Healthy male volunteers
  • Body mass index 18-30 kg/m2
  • Aged 18-35 and 65-75 years

Exclusion Criteria:

  • Participation in a formal exercise regime,
  • A BMI < 18 or > 30 kg/m2,
  • Active cardiovascular disease,
  • Taking beta-adrenergic blocking agents, statins or non-steroidal anti-inflammatory drugs,
  • Cerebrovascular disease,
  • Respiratory disease,
  • Metabolic disease,
  • Active inflammatory bowel or renal disease,
  • Malignancy,
  • Recent steroid treatment (within 6 months) or hormone replacement therapy,
  • Clotting dysfunction,
  • Musculoskeletal or neurological disorders,
  • Family history of early (<55y) death from cardiovascular disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Old Control
Older individuals (65-75 y) with no exercise intervention
Experimental: Old Concentric
Older individuals (65-75 y) studied before and after 8 weeks concentric exercise training
8 weeks concentric exercise training, 3 x per week, 60% 1-RM; 4 x 12-15 repetitions, 2 min rest between sets
Experimental: Old Eccentric
Older individuals (65-75 y) studied before and after 8 weeks eccentric exercise training
8 weeks eccentric exercise training, 3 x per week, 60% 1-RM; 4 x 12-15 repetitions, 2 min rest between sets
No Intervention: Young Control
Young individuals (18-30 y) with no exercise intervention
Experimental: Young Concentric
Young individuals (18-30 y) studied before and after 8 weeks concentric exercise training
8 weeks concentric exercise training, 3 x per week, 60% 1-RM; 4 x 12-15 repetitions, 2 min rest between sets
Experimental: Young Eccentric
Young individuals (18-30 y) studied before and after 8 weeks eccentric exercise training
8 weeks eccentric exercise training, 3 x per week, 60% 1-RM; 4 x 12-15 repetitions, 2 min rest between sets

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle protein synthesis
Time Frame: 0 - 8 weeks
Comparison of muscle protein synthesis using D2O in young and older individuals and in response to 8 weeks concentric or eccentric exercise training
0 - 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Tendon protein synthesis
Time Frame: 0 - 8 weeks
Comparison of tendon protein synthesis in young and older individuals and in response to 8 weeks concentric or eccentric exercise training
0 - 8 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle function
Time Frame: 0 - 8 weeks
Muscle strength, force and power in young and older individuals and in response to 8 weeks concentric or eccentric exercise training
0 - 8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Marco V Narici, PhD, University of Nottingham

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2014

Primary Completion (Actual)

May 1, 2017

Study Completion (Actual)

May 1, 2017

Study Registration Dates

First Submitted

May 16, 2014

First Submitted That Met QC Criteria

May 19, 2014

First Posted (Estimate)

May 20, 2014

Study Record Updates

Last Update Posted (Actual)

October 30, 2017

Last Update Submitted That Met QC Criteria

October 27, 2017

Last Verified

October 1, 2017

More Information

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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