Home-based Transcranial Direct Current Stimulation in Fibromyalgia Patients
Primary Purpose
Fibromyalgia
Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Active-tDCS
Sham-tDCS
Sponsored by
About this trial
This is an interventional treatment trial for Fibromyalgia focused on measuring tDCS, chronic pain, fibromyalgia
Eligibility Criteria
Inclusion Criteria:
- have chronic pain fibromyalgia according to the criteria of the American College of Rheumatology
- Pain unresponsive to analgesics such as paracetamol, acetyl salicylic acid, Ibuprofen, Carisoprodol, Zanaflex (Tizanidine) and Codeine
- Give informed consent to participate after initial evaluation.
Exclusion Criteria:
- Pregnancy
- Treatment with carbamazepine and gabapentin
- The. Metallic implant in the brain
- Medical devices implanted in the brain
- Alcohol or drug abuse history in the last 6 months
- Suffering from severe depression (with score> 30 on the Beck Depression Inventory)
- History of neurological disorders
- Unexplained fainting History
- History of head trauma or momentary loss of consciousness (self reported)
- Neurosurgery History
- Decompensated systemic diseases, and chronic inflammatory diseases (lupus, rheumatoid arthritis, renal failure and hepatitis).
Sites / Locations
- Hospital de Clinicas de Porto Alegre
- Wolnei Caumo
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
Active-tDCs
Sham-tDCS
Arm Description
17 patients will receive Active-tDCS intervention (2mA, 30 min) at home.
17 patients will receive Sham-tDCS intervention (2mA, 30 min) at home.
Outcomes
Primary Outcome Measures
Pain level in fibromyalgia patients using home-based tDCS
Evaluate the level of pain in fibromyalgia patients before and after each home-based tDCS session. We will use numerical pain scale to do that.
Secondary Outcome Measures
Serum levels of Brain Derived Neurotrophic Factor (BDNF)
Measurement of serum levels of BDNF pre and pos application of home-based application of home-based tDCS
Serum levels of calcium-binding protein B (S100B)
Measurement of serum levels of S100B pre and pos application of home-based tDCS
Functional capacity
Measurement of functional capacity pre and pos application of home-based tDCS with functional capacity scale in chronic pain.
Catastrophic thinking
Measurement of catastrophic thinking pre and pos application of home-based tDCS with catastrophizing scale.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02652988
Brief Title
Home-based Transcranial Direct Current Stimulation in Fibromyalgia Patients
Official Title
Home-based Transcranial Direct Current Stimulation in Fibromyalgia Patients. Phase II, Randomized, Double-blind, Single-center Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Completed
Study Start Date
January 2016 (undefined)
Primary Completion Date
May 1, 2018 (Actual)
Study Completion Date
June 12, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Wolnei Caumo
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In this phase II, randomized, double-blind clinical trial, the investigators intended to evaluate the home-based effect of transcranial direct current stimulation (tDCS) in patients with fibromyalgia. This syndrome affects between 3-5% of the population in an age group 40-60 years also occurring in childhood and old age. Reaches 3.4% of women and 0.5% of men. Fibromyalgia is a chronic widespread pain syndrome in various parts of the body. The neuromodulation techniques have as a principle produce inhibition or cortical arousal. The tDCS is a non-invasive brain stimulation method used to modulate the cortical excitability, using a low intensity direct current (1-2mA) directed to the scalp via the cathode and anode electrodes. The current reaches the cortex, producing hyperpolarization or depolarization of the axonal membrane potential. Evidence has shown that this method is presented as a technique able to alter cortical and subcortical neural networks. This technique has been used to treat psychiatric disorders such as depression, acute mania, bipolar affective disorder, panic, hallucinations, obsessive compulsive disorder, schizophrenia, withdrawal, rehabilitation after stroke, pain syndromes such as neuropathic pain, migraine, pancreatitis pain chronic and fibromyalgia. The tDCS is a low cost technique, with virtually no side effects and which exerts therapeutic effect by neuromodulatory pathways by distinct pathways activated by the drugs. In this scenario falls within the importance of developing this device for home use by fibromyalgia patients, since it is easy to use and thereby enables maintaining the benefit observed in studies performed and supervised frequently used in care centers. The use of tDCS over the long term is not feasible in hospital by patients demands, sometimes every day or more than once a week, removing the patient from their activities, and cost shifting and overload the healthcare system. Therefore, the objective of this study is to evaluate the effect of home-based tDCS in fibromyalgia patients in long-term treatment.
Detailed Description
Will be included women aged between 18 and 65 years, chronic pain fibromyalgia according to the criteria of the American College of Rheumatology, pain unresponsive to analgesics such as paracetamol, acetylsalicylic acid, ibuprofen, Carisoprodol, Zanaflex (Tizanidine) and Codeine. And give informed consent to participate after initial evaluation. Primary outcome is to evaluate the effect of treatment with home-base tDCS in patients with fibromyalgia. Secondary outcomes are: compare the effect of active home-based tDCS and sham in cortical neurophysiological processes and subcortical to stimulation with TMS and standardized noxious stimuli with and without concomitant conditioned Pain Modulation (CPM) in pain threshold outcomes to the test mechanical pressure, heat-algesic stimulus, cortical excitability parameters [evoked rest motor (MEP) MEP enough to evoke amplitude of 1 mV peak to peak, silent period (SP), motor threshold (MT), variation in blood volume and oxygenation cortical motor area [oxy-hemoglobin concentrations (Hbo) / deoxy-hemoglobin (HBr)] optically functional neuroimaging (NIRS) and variation in the frequency of alpha and beta waves of motor area stimulated by tDCS assessed by electroencephalogram (EEG). In surrogate outcome, the investigators will compare the effect of active home-sham tDCS the tDCS in pain levels and functional capacity, catastrophic thinking, bookmark levels of neurotrophic activity (BDNF) and astrocytic (S100 beta).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
tDCS, chronic pain, fibromyalgia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Active-tDCs
Arm Type
Active Comparator
Arm Description
17 patients will receive Active-tDCS intervention (2mA, 30 min) at home.
Arm Title
Sham-tDCS
Arm Type
Sham Comparator
Arm Description
17 patients will receive Sham-tDCS intervention (2mA, 30 min) at home.
Intervention Type
Other
Intervention Name(s)
Active-tDCS
Intervention Description
Active home-based tDCS applied at home.
Intervention Type
Other
Intervention Name(s)
Sham-tDCS
Intervention Description
Sham home-based tDCS applied at home.
Primary Outcome Measure Information:
Title
Pain level in fibromyalgia patients using home-based tDCS
Description
Evaluate the level of pain in fibromyalgia patients before and after each home-based tDCS session. We will use numerical pain scale to do that.
Time Frame
Ffive days per week, during 12 weeks.
Secondary Outcome Measure Information:
Title
Serum levels of Brain Derived Neurotrophic Factor (BDNF)
Description
Measurement of serum levels of BDNF pre and pos application of home-based application of home-based tDCS
Time Frame
2 days
Title
Serum levels of calcium-binding protein B (S100B)
Description
Measurement of serum levels of S100B pre and pos application of home-based tDCS
Time Frame
2 days
Title
Functional capacity
Description
Measurement of functional capacity pre and pos application of home-based tDCS with functional capacity scale in chronic pain.
Time Frame
2 days
Title
Catastrophic thinking
Description
Measurement of catastrophic thinking pre and pos application of home-based tDCS with catastrophizing scale.
Time Frame
2 days
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
have chronic pain fibromyalgia according to the criteria of the American College of Rheumatology
Pain unresponsive to analgesics such as paracetamol, acetyl salicylic acid, Ibuprofen, Carisoprodol, Zanaflex (Tizanidine) and Codeine
Give informed consent to participate after initial evaluation.
Exclusion Criteria:
Pregnancy
Treatment with carbamazepine and gabapentin
The. Metallic implant in the brain
Medical devices implanted in the brain
Alcohol or drug abuse history in the last 6 months
Suffering from severe depression (with score> 30 on the Beck Depression Inventory)
History of neurological disorders
Unexplained fainting History
History of head trauma or momentary loss of consciousness (self reported)
Neurosurgery History
Decompensated systemic diseases, and chronic inflammatory diseases (lupus, rheumatoid arthritis, renal failure and hepatitis).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wolnei S Calmo, Ph.D
Organizational Affiliation
Hospital de Clínicas de Porto Alegre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de Clinicas de Porto Alegre
City
Porto Alegre
State/Province
Rio Grande Do Sul
ZIP/Postal Code
90.450-120
Country
Brazil
Facility Name
Wolnei Caumo
City
Porto Alegre
State/Province
Rio Grande Do Sul
Country
Brazil
12. IPD Sharing Statement
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Home-based Transcranial Direct Current Stimulation in Fibromyalgia Patients
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