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Efficacy of Microcurrent Therapy After Eccentric Exercise

Primary Purpose

Delayed Onset Muscle Soreness

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Microcurrent Therapy
Sham microcurrent therapy
Sponsored by
University of Liege
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Delayed Onset Muscle Soreness focused on measuring microcurent, pain, flexibility

Eligibility Criteria

18 Years - 25 Years (Adult)MaleAccepts Healthy Volunteers

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.

Sites / Locations

  • Liege University Hospital Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Sham microcurrent therapy

Microcurrent Group

Arm Description

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.

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.

Outcomes

Primary Outcome Measures

Intensity of pain (Visual analogue scale)

Secondary Outcome Measures

Flexibility of quadriceps and hamstrings muscles
Flexibility of quadriceps muscle was assessed by means of the Prone Quadriceps Flexibility test. Flexibility of hamstrings was assessed by means of the Straight Leg Raising (SLR) test
Functional test (Unilateral counter-movement jump)
Unilateral counter-movement jump
Pain sensibility threshold (Determined by using a dolorimeter)
Determined by using a dolorimeter
Isometric strength (Maximal voluntary contraction of knee flexor and extensor muscles)
Maximal voluntary contraction of knee flexor and extensor muscles

Full Information

First Posted
December 6, 2014
Last Updated
June 8, 2015
Sponsor
University of Liege
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1. Study Identification

Unique Protocol Identification Number
NCT02322489
Brief Title
Efficacy of Microcurrent Therapy After Eccentric Exercise
Official Title
Efficacy of Microcurrent Therapy After Eccentric Exercise
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
May 2015 (Actual)
Study Completion Date
June 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Liege

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delayed Onset Muscle Soreness
Keywords
microcurent, pain, flexibility

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sham microcurrent therapy
Arm Type
Sham Comparator
Arm Description
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.
Arm Title
Microcurrent Group
Arm Type
Experimental
Arm Description
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.
Intervention Type
Device
Intervention Name(s)
Microcurrent Therapy
Intervention Description
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
Intervention Name(s)
Sham microcurrent therapy
Intervention Description
Several electrodes are placed over the muscles involved in the provocative task. The microcurrent therapy is then started but lasts only for five seconds.
Primary Outcome Measure Information:
Title
Intensity of pain (Visual analogue scale)
Time Frame
baseline, post-provocative task, post-treatment, 48h follow-up, following days until pain disappears
Secondary Outcome Measure Information:
Title
Flexibility of quadriceps and hamstrings muscles
Description
Flexibility of quadriceps muscle was assessed by means of the Prone Quadriceps Flexibility test. Flexibility of hamstrings was assessed by means of the Straight Leg Raising (SLR) test
Time Frame
baseline, post-provocative task, post-treatment, 48h follow-up
Title
Functional test (Unilateral counter-movement jump)
Description
Unilateral counter-movement jump
Time Frame
baseline, post-provocative task, post-treatment, 48h follow-up
Title
Pain sensibility threshold (Determined by using a dolorimeter)
Description
Determined by using a dolorimeter
Time Frame
baseline, post-provocative task, post-treatment, 48h follow-up
Title
Isometric strength (Maximal voluntary contraction of knee flexor and extensor muscles)
Description
Maximal voluntary contraction of knee flexor and extensor muscles
Time Frame
baseline, post-provocative task, post-treatment, 48h follow-up

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christophe Demoulin, PhD
Organizational Affiliation
University of Liege
Official's Role
Principal Investigator
Facility Information:
Facility Name
Liege University Hospital Center
City
Liege
ZIP/Postal Code
4000
Country
Belgium

12. IPD Sharing Statement

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Efficacy of Microcurrent Therapy After Eccentric Exercise

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