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The effects of trans cranial direct current stimulation on brain through skull on somatic and psychiatric symptom of elderly women with fibromyalgia

The effects of trans cranial direct current stimulation on brain through skull on somatic and psychiatric symptom of elderly women with fibromyalgia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201606091959N8
Enrollment
50
Registered
2017-01-15
Start date
2016-11-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

fibromyalgia. fibromyalgia

Interventions

Intervention 1: In the active group, 20 minutes, 2mA direct current stimulation, Anode at primary motor cortex and cathode at right supra-orbital is given. Intervention 2: In the control group, 30 se
Treatment - Other
In the active group, 20 minutes, 2mA direct current stimulation, Anode at primary motor cortex and cathode at right supra-orbital is given.
In the control group, 30 seconds, 2mA stimulation with 5 seconds RAMP-UP and RAMP-Down current is given to make the patient have a similar emotion to active group at the skull

Sponsors

vice chancellor for research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with fibromyalgia according to ACR-90; older than 50 years and female; Medications the patient has not changed during the 8 weeks ago and medically was stable. Exclusion criteria: psychiatric disease or chronic pain disorder in medical evaluation; history of substance abuse; history of Neurological diseases; cardiac pace maker; history of deep brain stimulation surgery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before, after and 1 months after interventions. Method of measurement: Visual Analogue Scale questionnaire.

Secondary

MeasureTime frame
Function. Timepoint: before, after and 1 months after interventions. Method of measurement: FIQ Questionnair.;Depression. Timepoint: before, after and 1 months after interventions. Method of measurement: BDI Questionnair.;Quality of life. Timepoint: before, after and 1 months after interventions. Method of measurement: SF36 Questionnair.;Anexity. Timepoint: before, after and 1 months after interventions. Method of measurement: HAM Questionnair.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Zhale Zandie

Iran University of Medical Science

zhzandie@gmail.com+98 21 6651 3250

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026