Efficacy of Microcurrent Therapy After Eccentric Exercise

NCT ID: NCT02322489

Last Updated: 2015-06-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 15 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-01-31
• Study Completion Date: 2015-06-30

Brief Summary

15 participants will be included in the present study. They will attend two groups of three sessions (i.e. sessions 1-2-3 and sessions 4-5-6) spaced by 3 months:

• session 1 and 4 (performed a few days before the experimental session): session for participants to get familiarized with the test battery.
• session 2 and 5: experimental session (the test battery followed by the provocative task, the test battery, the one-hour "treatment" and the test battery again).
• session 3 and 6 (performed 2 days later): the test battery.

The test battery included flexibility, functional, pressure pain threshold tests.

The provocative task was an isokinetic eccentric task for knee flexors and extensors.

The treatment was either a microcurrent therapy or a placebo microcurrent therapy.

Detailed Description

Objective:

To study the efficacy of microcurrent to reduce DOMS (Delayed Onset Muscle Soreness) occuring after an eccentric exercise

Methods:

Experimental protocol

Participants will attend two groups of three sessions (i.e. sessions 1-2-3 and sessions 4-5-6) spaced by 3 months:

• session 1 and 4 (performed a few days before the experimental session): session for participants to get familiarized with the test battery.
• session 2 and 5: experimental session: the test battery followed by the provocative task, the test battery, the one-hour "treatment" (real microcurrents at one of the session and placebo microcurrents at the other one) and the test battery again.
• session 3 and 6 (performed 2 days later): the test battery.

Before starting session 2, patients will be randomized into the microcurrent group or the placebo microcurrent group. Three months later, participants will change of group.

The Test Battery: it will be conducted by a blind (to the treatment) investigator. It will include knee flexor and extensor flexibility tests, a functional test (unilateral " counter-movement jump "), a pain to measure pain threshold of thigh muscles and an isometric maximal voluntary contraction (MVC) test of knee flexors and extensors.

The Provocative task: 40 isokinetic eccentric contractions of knee flexors and extensors.

The one-hour Treatment: with the participant lying on an examination table, several electrodes were located over the muscles involved in the provocative task. The microcurrent therapy was then started. It was stopped after 5 seconds in the "Placebo group" and after one hour in the real "Microcurrent group". The microcurrents were delivered by the machine B-E-St®.

Follow-up: in addition to the 48hours follow-up (session 3/6), participants will fill in a pain visual analogue scale each day after the session 2/5.

Conditions

Delayed Onset Muscle Soreness

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

Sham microcurrent therapy

The participant is lying on an examination table for one hour; several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started but it lasts only for 5 seconds.

Group Type: SHAM_COMPARATOR

Sham microcurrent therapy

Intervention Type: DEVICE

Several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started but lasts only for five seconds.

Microcurrent Group

The participant is lying on an examination table for one hour; several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started.

Group Type: EXPERIMENTAL

Microcurrent Therapy

Intervention Type: DEVICE

Several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started and lasts for one hour.

Interventions

Microcurrent Therapy

Several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started and lasts for one hour.

Intervention Type: DEVICE

Sham microcurrent therapy

Several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started but lasts only for five seconds.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Asymptomatic subjects

Exclusion Criteria

• practice of sports >3h per week
• present pain in the lower limbs
• history of thigh muscle injuries
• recent injury (last 3 months) of the lower limbs
• recent (last 3 months) plyometric exercises or lower limbs strengthening program.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 25 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

University of Liege

OTHER

Sponsor Role: lead

Responsible Party

Christophe Demoulin

Main investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Christophe Demoulin, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Liege

Locations

Liege University Hospital Center

Liège, Liege, Belgium

Countries

Belgium

Other Identifiers

Microcurrent

Identifier Type: -

Identifier Source: org_study_id