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

March 5, 2014 updated by: Stephen Patterson, St Mary's University College

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

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

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

24

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

      • London, United Kingdom, TW1 4SX
        • St Marys Umiversity College

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 45 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Physically Active Males

Exclusion Criteria:

  • Muscular skeletal disorders

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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Ischemic Preconditioning
IPC (4 x 5 minute cycles @ 220 mmHg) with 5 min reperfusion between trials.
Placebo Comparator: Ischemic Preconditioning Placebo
Placebo (4 x 5 minute cycles @ 20mmHg) with 5 minutes between each cycle

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in maximal voluntary contraction
Time Frame: pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Isometric 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.

pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in Creatine kinase
Time Frame: pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Plasma 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

pre exercise, 24 hours post, 48 hours post and 72 hours post exercise
Change from baseline in Limb girth
Time Frame: pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Mid-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

pre exercise, 24 hours post, 48 hours post and 72 hours post exercise
Chnage from baseline in Vertical jump
Time Frame: pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Vertical 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

pre exercise, 24 hours post, 48 hours post and 72 hours post exercise
Change from baseline in Muscle soreness
Time Frame: pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Muscle 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

pre exercise, 24 hours post, 48 hours post and 72 hours post exercise

Collaborators and Investigators

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

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

July 1, 2013

Primary Completion (Actual)

November 1, 2013

Study Completion (Actual)

November 1, 2013

Study Registration Dates

First Submitted

July 15, 2013

First Submitted That Met QC Criteria

July 22, 2013

First Posted (Estimate)

July 25, 2013

Study Record Updates

Last Update Posted (Estimate)

March 6, 2014

Last Update Submitted That Met QC Criteria

March 5, 2014

Last Verified

March 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • IPCEIMD001

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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