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Neurostimulation and memory training in depression

Investigations on the recall of autobiographical memories and emotional regulation strategies in a clinical sample

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3xmkyy
Enrollment
Unknown
Registered
2020-09-22
Start date
2019-10-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Depression

Interventions

Group 1: 10 subjects with depression will receive 20 minutes of transcranial direct current stimulation associated with autobiographical memory training for five consecutive days Group2: 10 subjects w
Device
Behavioural
E02.331.800

Sponsors

Universidade Federal da Paraíba
Lead Sponsor
Universidade Federal da Paraíba
Collaborator

Eligibility

Age
18 Years to 50 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Brazil

Contacts

Public ContactMelyssa Galdino

Universidade Federal da Paraíba

melyssa_cavalcanti@hotmail.com55 (83) 3216-7200

Outcome results

None listed

Source: REBEC (via WHO ICTRP)