Pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women; age between 18 and 40 years; diagnosis of Endometriosis identified by imaging exams and the presence of clinical findings; cognitive ability to understand and answer questionnaires; tolerance to treatment with electrical stimulation; symptoms of Anxiety identified by the Hamilton Anxiety Scale; depressive symptoms identified above 16 on the Center for Epidemiological Studies – Depression Scale
Exclusion criteria
Exclusion criteria: Being in the puerperal period (up to 12 months postpartum); currently breastfeeding; history of brain surgery, tumors, dizziness, or epileptic disease; history of alcohol or drug abuse; having metallic implants in the head; complaint of severe headache, dizziness, or severe migraine within 6 hours after the application in more than two sessions of Transcranial Direct Current Stimulation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effects of active and sham Transcranial direct current stimulation on Anxiety and Depressive symptoms in individuals with Endometriosis | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the effects of the application of Transcranial direct current stimulation on the perception of pain in women with Endometriosis; to assess the effects of the application of Transcranial direct current stimulation on the quality of life in women with Endometriosis; to assess the effects of the application of Transcranial direct current stimulation on fatigue in women with Endometriosis; to evaluate the satisfaction with the use of Transcranial direct current stimulation after treatment for Endometriosis | — |
Countries
Brazil
Contacts
Universidade Federal do Rio Grande do Norte