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The Effect of Ischemic Pre-Conditioning on the Rate of Recovery Following Exercise-Induced Muscle Damage

The Effect of Ischemic Pre-Conditioning on the Rate of Recovery Following Exercise-Induced Muscle Damage: a Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01907841
Enrollment
24
Registered
2013-07-25
Start date
2013-07-31
Completion date
2013-11-30
Last updated
2014-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise-induced Muscle Damage

Keywords

Investigate IPC on EIMD

Brief summary

Strenuous exercise or exercise involving eccentric muscle contractions can lead to muscle damage and changes in muscle function; this is known as exercise-induced muscle damage (EIMD). It is known that brief, repeated periods of ischemia followed by reperfusion, known as Ischemic Preconditioning (IPC) cause a delay in cell injury in cardiac muscle as well as in various other organs. Therefore the purpose of this study is to: 1. Quantify the use of IPC in recovery following EIMD. 2. Identify any effect of IPC during recovery on muscle function

Interventions

OTHERIschemic Preconditioning

Sponsors

St Mary's University College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Physically Active Males

Exclusion criteria

* Muscular skeletal disorders

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in maximal voluntary contractionpre exercise, 24 hours post, 48 hours post and 72 hours post exerciseIsometric MVC of the participants' dominant knee extensors was assessed using a strain gauge. MVCs were performed for 3 s with a 60 s rest between each repetition. The change in MVC will be determined 24, 48 and 72 hours following pre exercise conditions.

Secondary

MeasureTime frameDescription
Change from baseline in Creatine kinasepre exercise, 24 hours post, 48 hours post and 72 hours post exercisePlasma CK was determined from an earlobe capillary blood sample. The sample (10 microlitres) was analysed immediately using an semi-automated clinical chemistry analyser. The change in CK will be determined 24, 48 and 72 hours following pre exercise conditions
Change from baseline in Limb girthpre exercise, 24 hours post, 48 hours post and 72 hours post exerciseMid-thigh and calf circumference was assessed as a measure of limb swelling using an anthropometric tape measure. Both measures were obtained with the participant in a standing position. The change in limb girth will be determined 24, 48 and 72 hours following pre exercise conditions
Chnage from baseline in Vertical jumppre exercise, 24 hours post, 48 hours post and 72 hours post exerciseVertical jump (VJ) performance was assessed using an electronic timing mat with hands placed on hips and participants dropping down to a self-selected level before jumping maximally. The change in VJ will be determined 24, 48 and 72 hours following pre exercise conditions
Change from baseline in Muscle sorenesspre exercise, 24 hours post, 48 hours post and 72 hours post exerciseMuscle soreness - Participants were asked to perform and hold a squat (90° knee angle) whilst they rated their perceived muscle soreness on a 200 mm visual analogue scale. The scale consisted of a line from 0 mm (no pain) to 200 mm (unbearably painful). The change in muscle soreness will be determined 24, 48 and 72 hours following pre exercise conditions

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026