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Trial registered on ANZCTR
Registration number
ACTRN12617000058370
Ethics application status
Approved
Date submitted
9/01/2017
Date registered
11/01/2017
Date last updated
11/01/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effects of leg resistance training with blood-flow restriction on unrestricted exercising arms: A validation study
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Scientific title
The effects of leg resistance training with blood-flow restriction on the muscle size of an unrestricted exercising arm compared with an inactive arm or both an active and inactive arm with traditional resistance leg exercise in healthy males aged 18-25 years.
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Secondary ID [1]
284842
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Older adult physical/functional performance
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Condition category
Condition code
Musculoskeletal
292548
292548
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0
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Normal musculoskeletal and cartilage development and function
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Physical Medicine / Rehabilitation
292572
292572
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0
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Other physical medicine / rehabilitation
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention is a seven-week training program where participants train at the lab three days per week (twenty sessions; 45 minute duration each). Exercises performed are three sets of bicep curls (50% 1 RM) performed by the dominant arm followed by four sets of bilateral knee flexion and leg extension exercises (30% 1 RM). The leg exercises are performed with pressurised cuffs applied to the most proximal portion of the upper legs to restrict blood-flow to the working muscles. These cuffs are inflated to a pressure equal to 60% of the pressure required to completely occlude blood-flow through the legs.
Participants are supervised/monitored throughout all training sessions by an exercise physiologist to ensure safety and adherence to the protocol.
Attendance is registered for all training sessions.
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Intervention code [1]
289619
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Treatment: Other
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Intervention code [2]
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Rehabilitation
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Comparator / control treatment
A training control group that performs an identical protocol to the intervention group without applied BFR.
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Control group
Active
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Outcomes
Primary outcome [1]
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Muscle cross-sectional area of the exercised arm - assessed via peripheral quantitative computed tomography (pQCT) scan at 50% Humerus length
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Assessment method [1]
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Timepoint [1]
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Seven weeks following training commencement (20 sessions)
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Primary outcome [2]
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Muscle strength of the exercised arm - assessed via 1-RM method for unilateral bicep curl exercise.
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Assessment method [2]
292425
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Timepoint [2]
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Seven weeks following training commencement (20 sessions)
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Secondary outcome [1]
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Muscle cross-sectional area of the dominant leg - assessed via pQCT scan at 25% Femur length.
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Assessment method [1]
308909
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Timepoint [1]
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Seven weeks following training commencement (20 sessions)
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Secondary outcome [2]
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Leg muscle strength - assessed via 1-RM method for bilateral leg extension and leg flexion exercises.
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Assessment method [2]
308911
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Timepoint [2]
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Seven weeks following training commencement (20 sessions)
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Secondary outcome [3]
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Muscle cross-sectional area of the inactive arm - assessed via peripheral quantitative computed tomography (pQCT) scan at 50% Humerus length
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Assessment method [3]
330691
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Timepoint [3]
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7 weeks following training commencement (20 sessions)
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Secondary outcome [4]
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Muscle strength of the inactive arm - assessed via 1-RM method for unilateral bicep curl exercise.
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Assessment method [4]
330692
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Timepoint [4]
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7 weeks following training commencement (20 sessions).
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Eligibility
Key inclusion criteria
Young healthy males (18-25 years)
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Minimum age
18
Years
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Maximum age
25
Years
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Sex
Males
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Those unable to satisfy the vigorous exercise requirements of the Adult Pre-exercise Screening System tool.
People that have performed regular resistance training in the last six months
People with diagnosed cardiovascular disease, uncontrolled hypertension, high resting blood pressure or heart rate.
People who cannot easily comfortably perform the exercise due to musculoskeletal injuries.
People in existing dependent or unequal relationships with project staff.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
1/03/2015
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Date of last participant enrolment
Anticipated
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Actual
1/05/2016
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Date of last data collection
Anticipated
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Actual
5/07/2016
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Sample size
Target
26
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Accrual to date
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Final
24
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
289447
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University
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Name [1]
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Centre for Physical Activity and Nutrition research, School of Exercise and Nutrition Sciences, Deakin University
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Address [1]
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221 Burwood Highway, Burwood, VIC 3125
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Stuart Warmington
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Address
Centre for Physical Activity and Nutrition research
School of Exercise and Nutrition Sciences
Deakin University
221 Burwood Highway
Burwood, VIC, 3125
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Country
Australia
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Secondary sponsor category [1]
288139
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Individual
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Name [1]
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Anthony May
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Address [1]
288139
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Centre for Physical Activity and Nutrition research
School of Exercise and Nutrition Sciences
Deakin University
221 Burwood Highway
Burwood, VIC, 3125
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Country [1]
288139
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Australia
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Other collaborator category [1]
278013
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Individual
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Name [1]
278013
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Aaron Russell
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Address [1]
278013
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Centre for Physical Activity and Nutrition research
School of Exercise and Nutrition Sciences
Deakin University
221 Burwood Highway
Burwood, VIC, 3125
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Country [1]
278013
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
291205
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Deakin University Human Research Ethics Committee
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Ethics committee address [1]
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Secretary HEAG-H Pro Vice-Chancellor's Office Faculty of Health he3.018 221 Burwood Hwy Burwood VIC 3125
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
291205
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Approval date [1]
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20/01/2014
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Ethics approval number [1]
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HEAG-H 2013-296
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Summary
Brief summary
This study comprises part of a PhD project. It aims to investigate whether light-load blood-flow restriction training in the legs can improve the muscle size of an active arm. This will be compared with the non-active arm of these participants that perform blood-flow restriction in the legs as well as either arm of participants who performed traditional light-load strength training. The purpose is to investigate whether muscle size adaptations are transferable between limbs. This will be investigated in a seven week strength training study in participants that perform either blood-flow restriction or traditional strength training in the legs.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Stuart Warmington
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Address
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Deakin University, 221 Burwood Hwy, Burwood, VIC 3125
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Country
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Australia
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Phone
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+61 3 9251 7013
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Stuart Warmington
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Address
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Deakin University, 221 Burwood Hwy, Burwood, VIC 3125
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Country
49223
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Australia
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Phone
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+61 3 9251 7013
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Fax
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Email
49223
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[email protected]
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Contact person for scientific queries
Name
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Stuart Warmington
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Address
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Deakin University, 221 Burwood Hwy, Burwood, VIC 3125
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Country
49224
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Australia
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Phone
49224
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+61 3 9251 7013
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Fax
49224
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Email
49224
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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