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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
Wolnei Caumo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring tDCS, chronic pain, fibromyalgia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

First Posted
October 28, 2015
Last Updated
August 1, 2018
Sponsor
Wolnei Caumo
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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

Citations:
PubMed Identifier
16762044
Citation
Arnold LM. Biology and therapy of fibromyalgia. New therapies in fibromyalgia. Arthritis Res Ther. 2006;8(4):212. doi: 10.1186/ar1971.
Results Reference
background
PubMed Identifier
24348701
Citation
Ablin J, Fitzcharles MA, Buskila D, Shir Y, Sommer C, Hauser W. Treatment of fibromyalgia syndrome: recommendations of recent evidence-based interdisciplinary guidelines with special emphasis on complementary and alternative therapies. Evid Based Complement Alternat Med. 2013;2013:485272. doi: 10.1155/2013/485272. Epub 2013 Nov 21.
Results Reference
background
PubMed Identifier
18576297
Citation
Bigatti SM, Hernandez AM, Cronan TA, Rand KL. Sleep disturbances in fibromyalgia syndrome: relationship to pain and depression. Arthritis Rheum. 2008 Jul 15;59(7):961-7. doi: 10.1002/art.23828.
Results Reference
background
PubMed Identifier
17559710
Citation
Boggio PS, Rigonatti SP, Ribeiro RB, Myczkowski ML, Nitsche MA, Pascual-Leone A, Fregni F. A randomized, double-blind clinical trial on the efficacy of cortical direct current stimulation for the treatment of major depression. Int J Neuropsychopharmacol. 2008 Mar;11(2):249-54. doi: 10.1017/S1461145707007833. Epub 2007 Jun 11.
Results Reference
background
PubMed Identifier
20551724
Citation
Bradley LA, Wohlreich MM, Wang F, Gaynor PJ, Robinson MJ, D'Souza DN, Mease PJ. Pain response profile of patients with fibromyalgia treated with duloxetine. Clin J Pain. 2010 Jul-Aug;26(6):498-504. doi: 10.1097/AJP.0b013e3181dee80e.
Results Reference
background
PubMed Identifier
11750180
Citation
Bymaster FP, Dreshfield-Ahmad LJ, Threlkeld PG, Shaw JL, Thompson L, Nelson DL, Hemrick-Luecke SK, Wong DT. Comparative affinity of duloxetine and venlafaxine for serotonin and norepinephrine transporters in vitro and in vivo, human serotonin receptor subtypes, and other neuronal receptors. Neuropsychopharmacology. 2001 Dec;25(6):871-80. doi: 10.1016/S0893-133X(01)00298-6.
Results Reference
background
PubMed Identifier
18848998
Citation
Burgmer M, Pogatzki-Zahn E, Gaubitz M, Wessoleck E, Heuft G, Pfleiderer B. Altered brain activity during pain processing in fibromyalgia. Neuroimage. 2009 Jan 15;44(2):502-8. doi: 10.1016/j.neuroimage.2008.09.008. Epub 2008 Sep 24.
Results Reference
background
PubMed Identifier
19962494
Citation
Clauw DJ. Fibromyalgia: an overview. Am J Med. 2009 Dec;122(12 Suppl):S3-S13. doi: 10.1016/j.amjmed.2009.09.006.
Results Reference
background
PubMed Identifier
20428412
Citation
Chappell AS, Bradley LA, Wiltse C, Detke MJ, D'Souza DN, Spaeth M. A six-month double-blind, placebo-controlled, randomized clinical trial of duloxetine for the treatment of fibromyalgia. Int J Gen Med. 2008 Nov 30;1:91-102. doi: 10.2147/ijgm.s3979.
Results Reference
background
PubMed Identifier
9305361
Citation
Chen R, Samii A, Canos M, Wassermann EM, Hallett M. Effects of phenytoin on cortical excitability in humans. Neurology. 1997 Sep;49(3):881-3. doi: 10.1212/wnl.49.3.881.
Results Reference
background
PubMed Identifier
17133529
Citation
Fregni F, Gimenes R, Valle AC, Ferreira MJ, Rocha RR, Natalle L, Bravo R, Rigonatti SP, Freedman SD, Nitsche MA, Pascual-Leone A, Boggio PS. A randomized, sham-controlled, proof of principle study of transcranial direct current stimulation for the treatment of pain in fibromyalgia. Arthritis Rheum. 2006 Dec;54(12):3988-98. doi: 10.1002/art.22195.
Results Reference
background
PubMed Identifier
16542193
Citation
Fregni F, Boggio PS, Nitsche MA, Marcolin MA, Rigonatti SP, Pascual-Leone A. Treatment of major depression with transcranial direct current stimulation. Bipolar Disord. 2006 Apr;8(2):203-4. doi: 10.1111/j.1399-5618.2006.00291.x. No abstract available.
Results Reference
background
PubMed Identifier
15863752
Citation
Fregni F, Boggio PS, Nitsche M, Pascual-Leone A. Transcranial direct current stimulation. Br J Psychiatry. 2005 May;186:446-7. doi: 10.1192/bjp.186.5.446. No abstract available.
Results Reference
background
PubMed Identifier
14558098
Citation
Giesecke T, Williams DA, Harris RE, Cupps TR, Tian X, Tian TX, Gracely RH, Clauw DJ. Subgrouping of fibromyalgia patients on the basis of pressure-pain thresholds and psychological factors. Arthritis Rheum. 2003 Oct;48(10):2916-22. doi: 10.1002/art.11272.
Results Reference
background
PubMed Identifier
19337439
Citation
Harris RE, Clauw DJ. Newer treatments for fibromyalgia syndrome. Ther Clin Risk Manag. 2008 Dec;4(6):1331-42. doi: 10.2147/tcrm.s3396.
Results Reference
background
PubMed Identifier
11097099
Citation
Lindell L, Bergman S, Petersson IF, Jacobsson LT, Herrstrom P. Prevalence of fibromyalgia and chronic widespread pain. Scand J Prim Health Care. 2000 Sep;18(3):149-53. doi: 10.1080/028134300453340.
Results Reference
background
PubMed Identifier
10080512
Citation
Manganotti P, Bongiovanni LG, Zanette G, Turazzini M, Fiaschi A. Cortical excitability in patients after loading doses of lamotrigine: a study with magnetic brain stimulation. Epilepsia. 1999 Mar;40(3):316-21. doi: 10.1111/j.1528-1157.1999.tb00711.x.
Results Reference
background
PubMed Identifier
16078356
Citation
Mease P. Fibromyalgia syndrome: review of clinical presentation, pathogenesis, outcome measures, and treatment. J Rheumatol Suppl. 2005 Aug;75:6-21. Erratum In: J Rheumatol Suppl. 2005 Oct;32(10):2063.
Results Reference
background
PubMed Identifier
23733529
Citation
Moore RA, Cai N, Skljarevski V, Tolle TR. Duloxetine use in chronic painful conditions--individual patient data responder analysis. Eur J Pain. 2014 Jan;18(1):67-75. doi: 10.1002/j.1532-2149.2013.00341.x. Epub 2013 Jun 3.
Results Reference
background
PubMed Identifier
17986164
Citation
Roizenblatt S, Fregni F, Gimenez R, Wetzel T, Rigonatti SP, Tufik S, Boggio PS, Valle AC. Site-specific effects of transcranial direct current stimulation on sleep and pain in fibromyalgia: a randomized, sham-controlled study. Pain Pract. 2007 Dec;7(4):297-306. doi: 10.1111/j.1533-2500.2007.00152.x. Epub 2007 Nov 6.
Results Reference
background
PubMed Identifier
22297885
Citation
Schestatsky P, Stefani LC, Sanches PR, Silva Junior DP, Torres IL, Dall-Agnol L, Balbinot LF, Caumo W. Validation of a Brazilian quantitative sensory testing (QST) device for the diagnosis of small fiber neuropathies. Arq Neuropsiquiatr. 2011 Dec;69(6):943-8. doi: 10.1590/s0004-282x2011000700019.
Results Reference
background
PubMed Identifier
17685881
Citation
Staud R. Treatment of fibromyalgia and its symptoms. Expert Opin Pharmacother. 2007 Aug;8(11):1629-42. doi: 10.1517/14656566.8.11.1629.
Results Reference
background
PubMed Identifier
12095460
Citation
Staud R, Smitherman ML. Peripheral and central sensitization in fibromyalgia: pathogenetic role. Curr Pain Headache Rep. 2002 Aug;6(4):259-66. doi: 10.1007/s11916-002-0046-1.
Results Reference
background
PubMed Identifier
21170277
Citation
Valle A, Roizenblatt S, Botte S, Zaghi S, Riberto M, Tufik S, Boggio PS, Fregni F. Efficacy of anodal transcranial direct current stimulation (tDCS) for the treatment of fibromyalgia: results of a randomized, sham-controlled longitudinal clinical trial. J Pain Manag. 2009;2(3):353-361.
Results Reference
background

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Home-based Transcranial Direct Current Stimulation in Fibromyalgia Patients

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