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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02142855
Other study ID # B13032014 SoMSGEM BBSRC3
Secondary ID
Status Completed
Phase N/A
First received May 16, 2014
Last updated October 27, 2017
Start date May 2014
Est. completion date May 2017

Study information

Verified date October 2017
Source University of Nottingham
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 2017
Est. primary completion date May 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 75 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
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
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

Locations

Country Name City State
United Kingdom University of Nottingham Derby Derbyshire

Sponsors (2)

Lead Sponsor Collaborator
University of Nottingham Biotechnology and Biological Sciences Research Council

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Other Muscle function Muscle strength, force and power in young and older individuals and in response to 8 weeks concentric or eccentric exercise training 0 - 8 weeks
Primary Muscle protein synthesis 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 Tendon protein synthesis Comparison of tendon protein synthesis in young and older individuals and in response to 8 weeks concentric or eccentric exercise training 0 - 8 weeks
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