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Table 1 Characteristics of all included studies

From: The effects of transcranial direct-current stimulation (tDCS) on pain intensity of patients with fibromyalgia: a systematic review and meta-analysis

Author, publication year

country

design

Active group (n)

Sham group (n)

active electrode location

Cathode location

tDCS protocol

Associated interventions/ form of tDCS

Side effects

Pain outcome used

Notes (aim, result, duration of effects last)

qualitative

 Roizenblatt et al., 2007 [32]

Brazil

RCT

11 (f)

 

M1

Right SO

Anodal,

2 mA,

20 min,

5 sessions in consecutive days

None

None

VAS

Aim: to investigate the effect of tDCS-induced pain reduction on sleep structure in FM

Result: tDCS stimulation can decrease pain only in M1 condition, and tDCS can change sleep structure, specific to the site of stimulation.

Duration of effect: NA

11 (f)

 

Left DLPFC

 

10

(f)

sham

Turned off after 30 s of stimulation

 Silva et al., 2017 [35]

Brazil

RCT, cross-over design

17/20

(f)

18/20

(f)

Left DLPFC

Right SO

Anodal, 1 mA,

20 min,

Single session

Go/No-go task

Minor: tingling, burning, and itching. In both conditions

HPTh, HPTo,

Aim: Anodal tDCS over the left DLPFC modulates attention and pain in fibromyalgia

Result: active stimulation increased HPTh and HPTo

Duration: NA

 Mendonca et al., 2016 [20]

Brazil

RCT

30 - f/m (tDCS/AE group (n = 15), tDCS group (n = 15))

15 (AE group)

Left M1

Right SO

Anodal, 2 mA,

20 min,

5 sessions, consecutive days over the first week.

AE on a treadmill, 40 min, 9 sessions over 4 weeks

Mild adverse effects, not different between groups.

VNS

Aim: to assess the effect of combined intervention of tDCS and AE on pain in FM

Result: the combination intervention is superior in pain reduction compared to individual treatments.

Duration of effect: after one month of intervention.

 De Ridder et al., 2017 [24]

Belgium

RCT, crossover design

19

19 matched healthy control (Crossover design, 2 weeks washout period between conditions)

Right Occipital nerve field (OCF)

Left OCF (C2 dermatome)

Anodal, 1.5 mA, 20 min, 3 sessions, every two days, over a week

None

None

NRS, PCS

Aim: to investigate the mechanisms behind the effect of OCF on pain in FM.

Result: active tDCS shows significant pain reduction compared to sham and baseline.

Duration of effects: NA

Sham

 Brietzke et al., 2020 [31]

Brazil

RCT

10 (f)

10 (f)

Left DLPFC

Right DLPFC

Anodal,

2 mA, 30 min, 60 sessions over 12 weeks (5 consecutive days minimum interval of 16 h)

None/ bifrontal HB-tDCS

Mild and transient: headache, itching, tingling, and local redness

VAS (global pain in last 24 h), B-PCP:S, PPT, HPTo,

Aim: To test the effectiveness of HB-tDCS over DLPFC in multiple sessions on daily pain scores.

Result: tDCS was superior to the sham group alone in reducing pain intensity. Levels of BDNF predicted better response

Duration of effect: NA

 Kang et al., 2020 [29]

South Korea

RCT

46

No sham group

Left M1

Right SO

Anodal, 2 mA, 20 min, 5 sessions, consecutive days.

pharmacotherapy

No serious adverse effect was reported.

VAS

Aim: to investigate the effects of add-on tDCS stimulation on pain in FM.

Result: tDCS is effective in pain reduction and other features in FM.

Duration of effects: after one month post-stimulation.

 Forogh et al., 2021 [27]

Iran

RCT

15 (f)

No sham group

Left DLPFC

Right SO

Anodal,

2 mA, 20 min, 3 sessions, over one week (every other day)

None

None

VAS

Aim: to compare the effects of rTMS and tDCS on pain and quality of life in FM

Result: pain intensity was significantly reduced in both groups, however, rTMS was more effective.

Duration of effect: just after course termination

 EL-Badawy et al., 2021 [25]

Egypt

RCT

15

No sham group – but the TMS group with n = 15 was examined

Left M1

Right SO

Anodal, 2 mA, 20 min, 8 sessions,

None

Local tingling, well-tolerated complaint of headache and dizziness

VAS

Aim: to compare the efficacy of rTMS and tDCS in pain reduction in FM

Result: both interventions were significantly efficient in pain reduction significantly, however, rTMS resulted in better improvement.

Duration of effects:

 Caumo et al., 2022 [23]

Brazil

RCT

24 (f)

24 (f)

Left DLPFC

Right DLPFC

Anodal, 2 mA, 20 min

None/ bifrontal HB- tDCS

Severe: burning sensation,

Mild: tingling, redness, headache, neck pain, mood swings, concentration difficulties

VAS, PCS, FIQ

Aim: to evaluate the efficacy and safety of home-based bifrontal tDCS in reducing pain and disability due to pain in FM

Result: positive effect

Duration of effects: NA

quantitative

 Fregni et al., 2006 [28]

Brazil

RCT

     

None

Mild, similar to sham: Sleepiness and headache were the most frequent

VAS

Same as study subjects in the Roizenblatt et al. study

Result: tDCS stimulation of M1 had significant pain reduction in FM compared to DLPF and sham group

Duration of effect: at least 3 weeks after stimulation

 Valle et al., 2009 [21]

Brazil

RCT

14 (f)

 

M1

Contralateral SO

2 mA,

20 min,

10 sessions, consecutive days

None

Minor and uncommon: tingling, skin redness. Same with the sham group

VAS

Aim: to investigate the effect of tDCS stimulation of M1 and DLPFC on FM

Result: M1 stimulation markedly decreases pain in FM but no evidence for the efficacy of DLPFC stimulation

Duration of effect: M1 stimulation reduces pain that persists for up to 2 months.

13 (f)

 

DLPFC

 

14 (f)

Sham (M1)

 Mendonca et al., 2011 [19]

Brazil,

RCT

6

 

Right SO

Left M1

Cathodal,

2 mA, 20 min

None

Mild tingling at the beginning, no side effects

VNS, PPT, total body area of pain

Aim: to determine the efficacy of tDCS with different active electrode positions on pain reduction in FM

Result: SO tDCS resulted in a significant pain reduction both as cathode and anode

Duration of effects: NA

6

Left M1

Right SO

6

Left M1

Right SO

Anodal, 2 mA, 20 min

6

Right SO

Left M1

 

6

Left M1

Right SO

Sham, current on only for the initial 30 s

 Villamar et al., 2013 [22]

USA

RCT, crossover design

16/18

Crossover design, participants have 3 different interventions with 7 days interval

Left M1

 

Anodal, 2 mA, 20 min, 1 session

None /HD-tDCS

Mild to moderate tingling or itching during both active and sham stimulation, which resolved over a few minutes

VNS, PPT, and others

Aim: short term effects of HD-tDCS on pain reduction in FM

Results: Immediately after stimulation only cathodal HD-tDCS was effective and 30 min after stimulation both active interventions resulted in better pain reduction than the sham.

Duration of effects: NA

Cathodal, 2 mA, 20 min, 3 sessions

sham

 Foerster et al., 2015 [26]

USA

RCT, crossover design

12 (f)

Crossover design, 7 days washout period between conditions

Left M1

Right SO

Active Anodal, 2mA, 20 min, 5 consecutive days

None

None

VAS

Aim: To investigate the effects of tDCS on brain metabolites and the predictive value of treatment efficacy in FM.

Result: tDCS reduced pain intensity. tDCS also have effects on the brain metabolites. Baseline levels of these metabolites predicted pain reduction after tDCS.

Duration of effects: NA

sham

 Fagerlund et al., 2015 [18]

Norway

RCT

24

24

Left M1

Right SO

Anodal, 2 mA, 20 min, 5 sessions, consecutive days

None

Skin redness, sleepiness, and tingling were reported same in the active and sham group. Acute mood changes were more reported in the sham group

VAS, PPT

Aim: to investigate the effect of tDCS stimulation on pain in FM

Result: tDCS has a small but significant effect on pain reduction in FM.Duration of effects: NA

 Junior et al., 2015 [34]

Brazil

RCT

10 (f)

10 (f)

Left M1

Right SO

Anodal, 1 mA, 20 min, 10 sessions, consecutive days.

None

None

VAS

Aim: to evaluate the effect of tDCS on pain and quality of life in FM.

Result: tDCS is effective in pain control of FM. patients

Duration of effects: NA

 Yoo et al., 2018 [6]

Belgium

RCT

20

 

Left DLPFC + ONS

Right SO

1.5 mA, 20 min, each intervention, 8 sessions over 4 weeks, sessions were 3 days apart.

ONS

Tingling and itching

NRS

Aim: to investigate the effect of adding prefrontal tDCS before ONS on pain and quality of life in FM.

Results: prefrontal tDCS did not change the pain compared to ONS-only group.

Duration of effects: NA

20

 

ONS alone

 
 

20

  

 To et al., 2017 [33]

Belgium

RCT

11

 

Left DLPFC

Right DLPFC

Anodal, 1.5 mA, 20 min, 8 sessions, in 4 weeks

None

None

NRS, PCS

Aim: to compare the effects of bifrontal and occipital tDCS on pain and fatigue in FM

Result: both bifrontal and occipital tDCS reduced pain scores, DLPFC also improved fatigue and provided more general relief than C2 stimulation

Duration of effects: NA

15

 

Left occipital

Right occipital

 

16

  

Initial 10 s of active stimulation and then inactive for 20 min, same number of sessions.

 Khedr et al., 2017 [30]

Egypt

RCT

18

18

Left M1

Right SO

Anodal, 2 mA, 20 min, 10 sessions, 5 consecutive days over two weeks.

None

Itching and redness of skin in only 3 cases from the active group.

VAS

Aim: to evaluate the effects of tDCS on pain, mood, and serum endorphin levels in the treatment of FM.

Results: M1-tDCS was able to improve pain in FM significantly. This effect is related to changes in serum endorphin levels

Duration of effects: at least one month after stimulation

 Melo et al., 2020 [8]

Brazil

RCT

11 (f)

 

Left M1

Right SO

Anodal, 2 mA, 20 min, 1 week (5 consecutive days)

None

None

VAS

Aim of study: To compare the effects of two tDCS protocols on pain and EEG alpha-2 oscillations in FM

Result: Both protocols reduced pain intensity without significant difference, but only those received for 5 consecutive days, showed a significant reduction in alpha-2 power in the frontal and parietal region

Duration of effects: NA

9 (f)

Anodal, 2 mA, 20 min, 2 weeks (10 consecutive days excluding weekends)

 

11

(f) − 5 consecutive days

   
  1. Abbreviations: HPTh Heat pain threshold, HPTo Heat pain tolerance, DLPFC, SO Supraorbital, VAS Visual analog scale, FIQ Fibromyalgia impact questionnaire, B-PCP:S Brazilian Portuguese version of the profile of chronic pain: screen, PPT Pain pressure threshold, HB-tDCS home-based tDCS, CIRS Cumulative illness rating scale, VNS Visual numerical scale, DASS-21 Depression anxiety stress scale-21, AE Aerobic exercise, ONS Occipital nerve stimulation, PCS Pain catastrophizing scale