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NCT Number: NCT03084094

Neuromodulation and Its Therapeutic Potentiality in Different Populations

One of the big challenges faced by researchers who act in rehabilitation science is the capacity to dispose integrative approaches for its utilization in clinical practice. The border profile of a physiotherapy researcher is to be in front of applied research amplification in experimental integrative approaches, involving the study of behavioral and physiological variables.

The rehabilitation process transcends the systems physiology and encompasses the cognitive behavioral feature of being adapted to the environment that surround us. It is now known by the scientific rehabilitation community the necessity for evidence based therapies and even more, therapeutic innovation. In both conditions, of health and illness, various options to use integrative approaches are today available in physiotherapy, including behavioral and physiological profiles of the individuals during physical activities, response to stress and in the field of chronic pain.

It is in the clinical routine of numerous rehabilitation centers the treatment of diseases that causes pain, being the leading figure in a physiotherapist work process. The innovative study of resources that can alter the pain state of this patients becomes primordial for routine clinical use, low cost and easy to apply. The therapeutic treatment for pain offered by a physiotherapist need new investigative options based in evidences from the association between the neuronal, behavioral and physiological responses where the brain is the central organ of this regulation. In this context, become increasingly more necessary the construction of investigative approaches in the purpose of reaching the clinical practice, in a reduced time lapse, once the great volume of information produced globally does not impact in short or medium term in new therapeutic recommendations.

Among the various chronic painful entities, it is presented the fibromyalgia (FM), painful diabetic polyneuropathy and primary dysmenorrhea because of its painful pathogenic complexity and its limited therapeutic against pain in rehabilitation process. The 3 painful entities presents the central nervous system as main participant of neurogenesis and maintenance of the painful state.

It is primordial importance that rehabilitation science improve methods of non invasive brain neuromodulation that allows, through excitation or inhibition of specific cortical areas in order to produce pain inhibition, providing a simple and low cost treatment to clinical routine. Technological advances and non invasive techniques to modulate brain function has been developed, among which transcranial direct current stimulation (tDCS) stands out. Basically, electrodes are placed in targeted brain regions that you want to stimulate or inhibit. Posteriorly, is applied a continuous electric current (0,4 - 2 mA) for a 3-20 minutes period, in order to modify cortical excitability. The stimulus of the anodic current increases cortical excitability whereas the stimulus of the cathodic current has an inhibitory effect.

Few are the research groups that address the issue of fibromyalgia, painful diabetic polyneuropathy and primary dysmenorrhea and the application of tDCS as research focus, being a border area for rehabilitation science and great potential in clinical use. Preliminary studies associates the use of tDCS with the decrease of painful state, however an approach of physical function and behavioral results needs greater investigation.

The purpose of the presented project is to present the tDCS as a new modality in physical rehabilitation for the patient with chronic pain of the 3 entities mentioned above. The study proposal is to present behavioral, social and physical results of tDCS application in this patients, suggesting a better quality of life and functionality of the individual.

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Universitário Onofre Lopes

Natal, Rio Grande do Norte, Brazil

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female gender aged from 18 to 65 year old, having a clinical diagnosis of Fibromyalgia given by a rheumatologist.

Exclusion criteria

  • Non-regulated psychiatric disorders (bipolar, main depression, schizophrenia)
  • Performing other types of treatment during the research
  • Performing physical activities

Treatment and study plan

Transcranial Direct Current Stimulation

Device

Non invasive brain modulation at a 2mA current during 20minutes

Primary outcomes

  1. Change from Baseline Pain at 2 weeks

    Time frame: 1 week prior to treatment (Baseline) and 1 week during treatment

    Diary of Pain

  2. Change from Baseline Pain at 5 weeks

    Time frame: 1 week prior to treatment, day 1 of treatment, last day of treatment (day 5), 7 days, 14 days and 21 days after treatment

    Pressure Pain Threshold and Tolerance by an algometer

  3. Change from Baseline Pain at 5 weeks

    Time frame: 1 week prior to treatment, day 1 of treatment, last day of treatment (day 5), 7 days, 14 days and 21 days after treatment

    Visual Analogue Scale

Secondary outcomes

  1. Functional Capacity

    Time frame: 1 week prior to treatment, last day of treatment (day 5),7 days, 14 days and 21 days after treatment

    Fibromyalgia Impact Questionnaire

  2. Mood

    Time frame: 1 week prior to treatment, last day of treatment (day 5),7 days, 14 days and 21 days after treatment

    Beck Depression Inventory

  3. Anxiety

    Time frame: 1 week prior to treatment, last day of treatment (day 5),7 days, 14 days and 21 days after treatment

    Hamilton Anxiety Scale

  4. Positive and negative affect

    Time frame: 1 week prior to treatment, last day of treatment (day 5),7 days, 14 days and 21 days after treatment

    Positive and Negative Affect Schedule

Sponsors and collaborators

Lead sponsor

Universidade Federal do Rio Grande do Norte

Other

Registry information

Official study title

Transcranial Direct Current Stimulation and Its Therapeutic Potentiality in Different Populations

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Mar 20, 2017
Registry last updated
Jul 6, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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