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Electromechanical DissociationNCT01379105

Electromyographic Responses by Static Stretching and Neural Mobilization

A study testing neural mobilization and Static Stretching in people with Electromechanical Dissociation, run by Euro-American Network of Human Kinetics at 1 site in Brazil.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of this experimental study was to compare the electromyographic responses of sedentary youth with and without the administration of static stretching and neural mobilization. Read more about this study

Who is it for?
Ages 17 to 30 years, men onlyHealthy volunteers can take part
Conditions the study is for
Electromechanical Dissociation
What is being tested?
neural mobilization and Static Stretching
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteBrazil
Study dates
Aug 2010to Oct 2010
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 17 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • students with the absence of neural, muscular and skeletal-associated problems
  • who were non-obese, according to established body mass index

Who cannot join

  • if they had metabolic disease
  • neuro-musculo-skeletal problems,
  • practiced certain physical activities,
  • presented pain during maintenance of the position for electromyographic response collection or otherwise did not fulfill the terms of the agreement with the researcher.

Trial locations and contacts

1 site in 1 country.

Brazil1 site
  • College Santo Agostinho

    Teresina, Piauí, 64079-330

Other trials in Brazil

About this study

Official title: Electromyographic Responses of Sedentary Students Submitted to Static Stretching and Neural Mobilization

The objective of this experimental study was to compare the electromyographic responses of sedentary youth with and without the administration of static stretching and neural mobilization. The sample was composed of sedentary students, divided, randomly, into neural mobilization practitioners (NMG; n=15; age=22±3 years), static stretching practitioners (SSG; n=15; age=23±4 years) and a control group (CG; n=15; age: 24±4 years). For this evaluation, an electromyograph (EMG; a four channel system) was used to monitor electrical activity in the femoral bicep muscles). In neural mobilization, hip flexion was conducted passively with the knee extended, and 30 plantar-to-dorsal flexion oscillations were completed per minute. For the static stretching, hip flexion with was completed passively with the knee extended and held for 6 seconds. The perception of effort was evaluated using the Perceived Force in Flexibility Scale. The statistical significance level was p<0.05. Descriptive statistics such as the average, standard deviation, median, standard error and absolute change within groups (post-test - pretest) were calculated. The sample normality was evaluated using the Shapiro-Wilk test. For the response variable analysis, the paired Student's t-test (paired) or Wilcoxon test (nonparametric) was used for intragroup analysis. For the intergroup analysis, the multivariate analysis of variance (ANOVA) test was used, followed by the Tukey Post-Hoc test. A p<0.05 significance level was adopted for the statistical evaluations. Microsoft Excel and the Statistical Package for Social Science (SPSS) version 14.0 were used for evaluation of the results.

Read the detailed description

This study was approved by the Committee for Ethics in Research with Humans of the Faculty of Medical Sciences (FACIME) (protocol number 145/09).

The group included students with the absence of neural, muscular and skeletal-associated problems and who were non-obese, according to established body mass index (BMI) criteria. Participants were excluded if they had metabolic disease or neuro-musculo-skeletal problems, practiced certain physical activities, presented pain during maintenance of the position for electromyographic response collection or otherwise did not fulfill the terms of the agreement with the researcher.

In the first stage, the researcher conducted an anamnesis of the individuals to obtain information about their dietary habits (Vasconcelos, 1995), medicines being used, pathological history and physical activity, according to the Baecke Questionnaire (Florindo, Latorre, 2003). In the second stage, the subjects' heights and body mass were measured for body mass index (BMI) evaluation using a Filizola 0-150 kg clinical scale (with a precision of 0.1 kg) and a mechanical 0-190 cm stadiometer (with a precision of 0.5 cm), following the recommendations of the International Society for the Advancement of Kinanthropometry (Marfell-Jonnes et al., 2006).

For the electromyography measurements, the subject was positioned in dorsal decubitus on a São Paulo Institute (ISP) model 4040 couch, and the researcher performed hip flexion and knee extension until tissue resistance, at which point the volunteer reported the sensation of "discomfort combined with pain'' by pressing a trigger button, and the signal was recorded for 2 seconds after this point. The speed with which the movements were made was slow and gradual, because, according to reports from Tanaka and Farah (2007), for the same degree of the range of motion, a greater stretching speed generates a higher impulse frequency in the afferent fibers near the terminal, such that a more intense reflex response is promoted.

The electrical activity of the femoral bicep muscle of the right thigh was recorded by a four channel EMG system with using superficial bipolar active electrodes (pre-amplified) with acquisition software and signal processing. The sampling frequency was 2,000 Hz, and the amplifier had a high-pass filter at 20 Hz and a low-pass filter at 500 Hz; a 12-bit analogical converter and computer completed the system.

In both interventions (SSG and NMG), the perception of strength was evaluated using the Perceived Strength and Flexibility Scale (PERFLEX)which presents five levels of intensity, varying from 0 to 110, with five corresponding verbal descriptors, so that the evaluated individual can point to the description of their perception corresponding to the amplitude of movement performed.

In the SSG group, the subject was positioned in dorsal decubitus, and the researcher performed hip flexion with the knee extended passively and held for 30 seconds; this type of stretching corresponds to the maintenance of increased amplitude posture, without surpassing the maximum movement limit, three times with an interval of 10 seconds between the repetitions (Nelson and Bandy, 2005). In the NMG group, the subject was positioned in dorsal decubitus, and the researcher performed hip flexion with the knee extended passively and performed 30 oscillations of plantar-to-dorsal flexion for one minute. In the SSG group, the subject was positioned in dorsal decubitus, and the researcher performed hip flexion with the knee extended passively and held for 30 seconds; this type of stretching corresponds to the maintenance of increased amplitude posture, without surpassing the maximum movement limit, three times with an interval of 10 seconds between the repetitions (Nelson and Bandy, 2005). In the NMG group, the subject was positioned in dorsal decubitus, and the researcher performed hip flexion with the knee extended passively and performed 30 oscillations of plantar-to-dorsal flexion for one minute.

Being tested
neural mobilization, Static Stretching
Keywords
Electromyography, Muscle Stretching Exercises, Neuromuscular agents, Sedentary Lifestyle
Medical subject headings
Sedentary Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • neural mobilizationOther

    Also called NM

    In the neural mobilization group, the subject was positioned in dorsal decubitus, and the researcher performed hip flexion with the knee extended passively and performed 30 oscillations of plantar-to-dorsal flexion for one minute

  • Static StretchingOther

    Also called Stretching

    In the static stretching group, the subject was positioned in dorsal decubitus, and the researcher performed hip flexion with the knee extended passively and held for 30 seconds; this type of stretching corresponds to the maintenance of increased amplitude posture, without surpassing the maximum movement limit, three times with an interval of 10 seconds between the repetitions.

Study groups in NCT01379105
Study groupRoleWhat they receive
electromyographyOtherThe electrical activity of the femoral bicep muscle of the right thigh was recorded by a four channel EMG system with using superficial bipolar active electrodes (pre-amplified) with acquisition software and signal processing. The sampling frequency was 2,000 Hz, and the amplifier had a high-pass filter at 20 Hz and a low-pass filter at 500 Hz; a 12-bit analogical converter and computer completed the system
Receives: Other: neural mobilization; Other: Static Stretching

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. electromyography response

    For the electromyography measurements, the researcher performed hip flexion and knee extension until tissue resistance, at which point the volunteer reported the sensation of "discomfort combined with pain'' by pressing a trigger button, and the signal was recorded for 2 seconds after this point. The speed with which the movements were made was slow and gradual, for the same degree of the range of motion, a greater stretching speed generates a higher impulse frequency in the afferent fibers near the terminal, such that a more intense reflex response is promoted.

    Measured: four seconds to take the signal

Secondary outcomes (1)
  1. Flexibility effort

    In both interventions (neural mobilization - NMG and static stretching - SSG), the perception of stretching was evaluated using the Perceived Strength and Flexibility Scale (PERFLEX), which presents five levels of intensity, varying from 0 to 110, with five corresponding verbal descriptors, so that the evaluated individual can point to the description of their perception corresponding to the amplitude of movement performed: 0 to 30, "normal"; 31 to 60, "strain"; 61 to 80, "discomfort"; 81 to 90, "bearable pain"; and 91 to 110, "strong pain".

    Measured: 30 seconds

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jun 2011 (estimated)
  2. Study startAug 2010
  3. Primary completionSep 2010
  4. Study completionOct 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01379105
Sponsor's protocol ID
0111
Status last verified
Jun 2011
First submitted
20 Jun 2011
Last updated
23 Jun 2011
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing neural mobilization and Static Stretching in people with Electromechanical Dissociation, run by Euro-American Network of Human Kinetics at 1 site in Brazil.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Jun 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

electromyography response (time frame: four seconds to take the signal). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Jun 2011.

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