eurostimulation and memory training in depressio

Not Applicable

Terminated

• Conditions: Depression; F01.145.126.350

• Registration Number: RBR-3xmkyy
• Lead Sponsor: niversidade Federal da Paraíba

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-09-22
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Terminated
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Volunteers aged 18 to 50 years old, regardless of gender; presenting symptoms of moderate to severe depression by BDI; not being pregnant; not having metallic or electronic devices implanted in the head; not having a history of alcohol or drug abuse in the last 6 months; not using carbamazepine in the last 6 months; not having a history of epilepsy, stroke, moderate severe traumatic brain injury, or migraine; not having undergone neurosurgery; not having schizophrenia or bipolar disorder.

Exclusion Criteria

A fault during the treatment sessions, during the research;meet any of the aforementioned inclusion criteria, as in the case of women, becoming pregnant.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
At the end of the intervention, a reduction in symptoms of depression is expected in the groups undergoing intervention, as measured by the Beck Depression Scale (BDI) and the Hamilton Scale. .

Secondary Outcome Measures

Name	Time	Method
It is expected that at the end of the intervention, the positive affect will be increased compared to the beginning, and to the use of the intervention. The PANAS scale will be used.