- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07573709
Functional and Affective Effects of a Brief tDCS Intervention in Fibromyalgia and Chronic Fatigue Syndrome (FibFatDCS)
Studieöversikt
Status
Betingelser
Detaljerad beskrivning
Abstract Background: Fibromyalgia (FM) and chronic fatigue syndrome (CFS) are characterized by persistent, multidimensional symptoms arising from complex brain-body interactions that impair functioning and quality of life. Noninvasive neuromodulation techniques such as transcranial direct current stimulation (tDCS) have been proposed as adjunctive approaches to support short-term functional changes within distributed neural systems, although evidence remains limited and heterogeneous. Objective: To examine immediate pre-post changes in multidimensional clinical outcomes following a standardized tDCS protocol in patients with FM and CFS, and to explore potential diagnosis-related response patterns. Methods: Fifteen patients (FM: n = 5; CFS: n = 10) received 10 sessions of tDCS (20 minutes per session) administered over two consecutive weeks (five sessions per week). Patient-reported outcomes were assessed at baseline and immediately after treatment completion. Measures included the Short Form-36 Health Survey (SF-36), Fibromyalgia Impact Questionnaire (FIQ), Hospital Anxiety and Depression Scale (HADS), Composite Autonomic Symptom Score (COMPASS), pain thermometer, Epworth Sleepiness Scale, Fatigue Severity Scale (FSS), and Fatigue Assessment Scale (FAS). Pre-post comparisons were conducted at the whole-sample level, followed by exploratory analyses stratified by diagnosis. Results: At baseline, patients with FM showed lower COMPASS, FSS, FAS, and HADS scores, and higher SF-36 scores, compared to patients with CFS, indicating a relatively less severe clinical profile. Across the sample, pre-post comparisons indicated improvements in FIQ and HADS scores. Exploratory group-specific analyses suggested that FM patients exhibited reductions in depressive symptoms, whereas CFS patients showed improvements in quality of life (SF-36) and functional impact (FIQ). No significant changes were observed in subjective pain intensity or fatigue severity (FSS). Conclusions: These findings suggest partially distinct clinical profiles and differential responsiveness to tDCS across FM and CFS, within the context of baseline differences between groups. Improvements appeared domain-specific, with affective symptoms responding in FM and functional outcomes in CFS, while core symptoms such as pain and fatigue remained unchanged over the intervention period. This pattern provides preliminary support for the idea that short-term neuromodulation may preferentially influence higher-order regulatory processes rather than core symptom generators, underscoring the need for tailored, multidimensional treatment approaches. Nevertheless, given the small sample size, absence of a control condition, and exploratory nature of subgroup analyses, these results should be interpreted with caution. Further controlled
studies are needed to clarify the reliability, specificity, and clinical relevance of these effects.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Gipuzkoa
-
San Sebastián, Gipuzkoa, Spanien, 20250
- Hospital Universitario de Donostia
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Beskrivning
Inclusion Criteria:
- Diagnosis of Fibromyalgia
- Diagnosis of chronic fatigue syndrome
Exclusion Criteria:
- Having both conditions at the same time
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: The patients with Fibromyalgia
The same treatment is applied (tDCS)
|
It is an neuromodulation technic
|
|
Aktiv komparator: The patients with chronic fatigue syndrome
The same treatment is applied ( tDCS)
|
It is a neuromodulation technic
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Visual Pain Scores (VAS)
Tidsram: From enrollment to the end of treatment at 2 weeks
|
It is measured before and inmediately after the treatment ( tDCS) is applied.
(0-10) Higher scores mean more pain.
|
From enrollment to the end of treatment at 2 weeks
|
|
Fibromyalgia Impact Questionnaire (FIQ)
Tidsram: From enrollment to the end of treatment at 2 weeks
|
It measures the impact of fibromyalgia (Scores: 0-100) The FIQ is scored in such a way that a higher score indicates a greater impact of the syndrome on the person.
|
From enrollment to the end of treatment at 2 weeks
|
Samarbetspartners och utredare
Sponsor
Utredare
- Studierektor: Adolfo Lopez de Munain, Doctor, University Hospital of Donostia
- Studierektor: PEDRO MONTOYA, UNIVERSITY OF BALEARIC ISLANDS, MALLORCA
Publikationer och användbara länkar
Allmänna publikationer
- Moldofsky H. Fibromyalgia, sleep disorder and chronic fatigue syndrome. Ciba Found Symp. 1993;173:262-71; discussion 272-9. doi: 10.1002/9780470514382.ch15. PMID: 8491102.
- McHorney CA, Ware JE Jr, Lu JF, Sherbourne CD. The MOS 36-item Short-Form Health Survey (SF-36): III. Tests of data quality, scaling assumptions, and reliability across diverse patient groups. Med Care. 1994 Jan;32(1):40-66. doi: 10.1097/00005650-199401000-00004. PMID: 8277801.
- Lloyd, D. M., Wittkopf, P. G., Arendsen, L. J., & Jones, A. K. P. (2020). Is transcranial direct current stimulation (tDCS) effective for the treatment of pain in fibromyalgia? A systematic review and meta-analysis. The Journal of Pain, 21(11-12), 1085-1100. https://doi.org/10.1016/j.jpain.2020.01.003
- Lerdal A, Kottorp A. Psychometric properties of the Fatigue Severity Scale-Rasch analyses of individual responses in a Norwegian stroke cohort. Int J Nurs Stud. 2011 Oct;48(10):1258-65. doi: 10.1016/j.ijnurstu.2011.02.019. Epub 2011 Mar 16. PMID: 21414620.
- Hendriks C, Drent M, Elfferich M, De Vries J. The Fatigue Assessment Scale: quality and availability in sarcoidosis and other diseases. Curr Opin Pulm Med. 2018 Sep;24(5):495-503. doi: 10.1097/MCP.0000000000000496. PMID: 29889115
- Hawker, G. A., et al. (2011).Measures of adult pain: Visual Analog Scale for Pain (VAS Pain). Arthritis Care & Research, 63(S11), S240-S252. https://doi.org/10.1002/acr.20543
- Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome; Board on the Health of Select Populations; Institute of Medicine. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Redefining an Illness. Washington (DC): National Academies Press (US); 2015 Feb 10. 7, Recommendations. Available from: https://www.ncbi.nlm.nih.gov/books/NBK284910/
- Burckhardt CS1, Clark SR, Bennett RM. The fibromyalgia impact questionnaire: development and validation.J Rheumatol. 1991 May;18(5):728-33.
- Bartholomew EJ, Medvedev ON, Petrie KJ, Chalder T. Rasch analysis of the hospital anxiety and depression scale in patients with chronic fatigue syndrome. J Psychosom Res. 2025 Oct;197:112370. doi: 10.1016/j.jpsychores.2025.112370. Epub 2025 Sep 3. PMID: 40939313.
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Neuroinflammatoriska sjukdomar
- Neurologiska manifestationer
- Muskuloskeletala sjukdomar
- Sjukdomar i nervsystemet
- Muskelsjukdomar
- Patologiska processer
- Encefalomyelit
- Neuromuskulära sjukdomar
- Kronisk sjukdom
- Sjukdomsegenskaper
- Reumatiska sjukdomar
- Patologiska tillstånd, tecken och symtom
- Tecken och symtom
- Smärta
- Trötthetssyndrom, kronisk
- Fibromyalgi
- Trötthet
Andra studie-ID-nummer
- #061CER24
- European Regional Development (Annan identifierare: grant #PID2022-140561NB-I00.)
Plan för individuella deltagardata (IPD)
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