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Effects of brain stimulation in people with Anxiety Disorder

Effects of Transcranial Direct Current Stimulation in persons suffered by Generalized Anxiety Disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5qjg9t
Enrollment
Unknown
Registered
2019-04-03
Start date
2018-12-10
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

Generalized Anxiety Disorder

Interventions

This research is an Experimental Study and has as its outline the triple-blind randomized clinical trial with two arms, ensuring that the participants are being randomly distributed in the experimenta
Device
E02.331.750

Sponsors

Universidade Federal do Rio Grande do Norte
Lead Sponsor
Universidade Federal do Rio Grande do Norte
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Be between 20 and 40 years old; clinical diagnosis according to the criteria of the American Psychiatric Association - DSM-V (2014), of TAG; not going through psychotherapy at the time of the study; ability to understand the purpose of the research and to answer the scales and questionnaires.

Exclusion criteria

Exclusion criteria: Be pregnant at the time of data collection; have a metallic, cerebral or pacemaker implant; history of epileptic disease, convulsive crisis and dependence on alcohol or narcotic substance.

Design outcomes

Primary

MeasureTime frame
Decreased anxiety symptoms evaluated using the anxiety scales (Beck scale of anxiety, below 8 points and the Hamilton anxiety scale that has 9 as cutoff point) after and before intervention.

Secondary

MeasureTime frame
Decreased of depression levels evaluated by Beck depression scale with decreasing from high or moderate depression to low depressionafter and before intervention.

Countries

Brazil

Contacts

Public ContactAna Lima

Universidade Federal do Rio Grande do Norte

analucialimaa@gmail.com+55-084-994710000

Outcome results

None listed

Source: REBEC (via WHO ICTRP)