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Effects of Ischemic Preconditioning on Muscle Damage Induced by Excentric Exercise

Effects of Ischemic Preconditioning on Muscle Damage Induced by Excentric Exercise: Randomized Clinical Trial Placebo Controlled

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04420819
Enrollment
80
Registered
2020-06-09
Start date
2021-04-01
Completion date
2022-04-01
Last updated
2022-04-26

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

Conditions

Healthy

Keywords

Ischemic Preconditioning, Exercise, Musculoskeletal Pain, Creatine Kinase, Muscle Fatigue, Stress, Physiological

Brief summary

Introduction: eccentric exercise (EE) has been widely used in rehabilitation and in improving physical fitness due to its mechanical advantage and less metabolic demand, however, EE can induce muscle damage providing structural changes and reduced muscle function, therefore, it is necessary to look for alternatives to reduce this damage caused by stress. Thus, ischemic preconditioning (PCI) can be seen as an aid in reducing the damage caused by EE, as it can attenuate the ischemia-reperfusion injury, and can be used to accelerate the post-exercise recovery process. Objectives: to compare the effects of PCI, using different occlusion pressures, on acute and late responses to perceptual outcomes and muscle injury markers, in addition to checking whether the technique causes deleterious effects on performance in post-exercise recovery. Methods: a randomized placebo controlled clinical trial will be conducted with 80 healthy men aged 18 to 35 years who will be randomly divided into four groups: PCI using total occlusion pressure (POT), PCI with 40% more than POT, placebo (10 mmHg) and control. The PCI protocol will consist of four cycles of ischemia and reperfusion of five minutes each. All groups will perform an EE protocol, initial assessments, immediately after the end of the EE, 24, 48, 72 and 96 hours after exercise, with the maximum isometric voluntary contraction (CVIM) assessed by the isokinetic dynamometer, vectors of cell integrity by by means of electrical bioimpedance (BIA), creatine kinase (CK), blood lactate, pain on the visual analog scale (VAS), pain threshold by the pressure algometer, and tone, muscle rigidity and elasticity by myotonometry. The descriptive statistical method and analysis of variance will be used for the repeated measures model. The level of significance will be p \<0.05.

Interventions

DEVICEIschemic Preconditioning

The IPC is characterized by the application of brief periods of circulatory occlusion (ischemia) and reperfusion of a limb in the minutes to hours that precede the exercise through the insufflations and deflations of a pressure cuff

Sponsors

Paulista University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* not having any health condition that contraindicates or prevents EE; * not having diagnosed diabetes and high blood pressure; * not having inflammatory, psychiatric, cardiovascular and / or respiratory rheumatic disease; * not being an alcoholic, using drugs and / or a smoker; * without a history of knee surgery (for example, meniscal repair and ligament reconstruction) or recent musculoskeletal injury to the lower limbs that may impair performance during tests or interventions (for example, muscle injury, tendinopathy, patellofemoral pain in the lower limbs and / or back pain in the last six months); * without involvement in any type of training program during the study period; * not being engaged in the lower limb strength training program during the three months prior to participating in the study; * not using ergogenic supplements to improve physical performance and / or muscle mass and / or vasoactive drugs; * not having one or more risk factors predisposing to thromboembolism.

Exclusion criteria

* present a health problem that does not allow continuity, * use medication, electrotherapy or other therapeutic means that may interfere with any result; * perform unusual or strenuous physical activities during the evaluation period; * want to leave the study.

Design outcomes

Primary

MeasureTime frameDescription
Muscle damageChange from baseline at 96 hours after exercisePlasma CK concentration will be obtained by means of 32 μL of capillary blood collected from the digital pulp.
Blood lactate concentrationChange from baseline at 96 hours after exerciseBlood lactate concentration of the participant will be collected 25 ml of blood with an ear lobe capillary
Muscle strength in isokineticChange from baseline at 96 hours after exerciseMaximal voluntary isometric contraction (MVIC)

Secondary

MeasureTime frameDescription
Pain thresholdChange from baseline at 96 hours after exerciseAssessed using pressure algometer equipment, and the pain threshold will be classified according to the cut-off point of 2.55kgf. Participants will be classified as sensitive to pain if they have values below 2.55kgf.
Resistance through Bioimpedance analysis (BIA)Change from baseline at 96 hours after exerciseEvaluation of tissue resistance, the higher the value, the worse the result
Tone muscular through Myotonometry used the MyotonPRO equipmentChange from baseline at 96 hours after exerciseNatural Oscillation Frequency \[Hz\], characterizing Tone of the quadriceps femoris muscle
Reactance through Bioimpedance analysis (BIA)Change from baseline at 96 hours after exerciseEvaluation of tissue reactance, the higher the value, the better the cell integrity
Elasticity through Myotonometry used the MyotonPRO equipmentChange from baseline at 96 hours after exerciseMechanical Stress Relaxation Time \[ms\] featuring muscle elasticity of the quadriceps femoris muscle
Perception of recoveryChange from baseline at 96 hours after exercisePerception of recovery was obtained using a 10-point Likert Scale, with a rating of 1 indicating the feeling not recovered and a rating of 10 the feeling fully recovered
Stiffness through Myotonometry used the MyotonPRO equipmentChange from baseline at 96 hours after exerciseDynamic Stiffness \[N/m\] of the quadriceps femoris muscle
Phase angle through Bioimpedance analysis (BIA)Change from baseline at 96 hours after exerciseAssessment of the phase angle, the higher the value, the better the condition of the participant
Muscle painChange from baseline at 96 hours after exerciseAssessed using a visual analog scale that ranges from 0 to 10 points, the higher the score, the worse the result.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026