Skip to content

Treatment of Depression in the elderly with Transcranial Magnetic Stimulation

Treatment of Depression in the elderly with repetitive Transcranial Magnetic Stimulation using the Theta Burst method: a randomized, double-blind clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2mfbfvp
Enrollment
Unknown
Registered
2024-08-12
Start date
2024-03-26
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

Moderate depressive episode

Interventions

This research consists of a double-blind clinical trial in which we will work with two randomly allocated groups: transcranial magnetic stimulation (TMS) with ACT intervention (experimental group or G

Sponsors

Faculdade de Medicina da Universidade de São Paulo
Lead Sponsor
Faculdade de Medicina da Universidade de São Paulo
Collaborator

Eligibility

Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Be over 60 years of age and have an initial Hamilton Scale (HDRS) score greater than 08.

Exclusion criteria

Exclusion criteria: Having other mental disorders (alcohol or drug addiction; psychotic disorders; dementia); presence of severe neurological or clinical diseases; presence of severe suicidal ideation, presence of psychotic symptoms, presence of severe depression characterized as HDRS greater than 28 points, with a CIRS score (Cumulative Illness Rating Scale) > 7, characterizing a set of clinical morbidities that may impair adherence to the protocol of research and presence of (hypo)manic symptoms demonstrated with more than 8 points on the Young Mania Rating Scale and bipolar rapid cyclers. In addition, specific contraindications to the use of rTMS also resulted in exclusion, such as metal implants, epilepsy or electronics in the cephalic segment.

Design outcomes

Primary

MeasureTime frame
Measure depressive symptoms using the Hamilton scale (HDRS) at the end of 6 weeks from the beginning of the first day of TBS.

Secondary

MeasureTime frame
Measure depressive symptoms, as well as remission data (decrease of at least 50% of the Hamilton scale - HDRS - initial) and response (HDRS = 7) using the sixth week scales: MADRS (Montgomery-Asberg Depression Rating Scale), GDS (Geriatric Depression Scale), CIRS (Cumulative Illness Rating Scale) and the clinical global impression scale (CGI).

Countries

Brazil

Contacts

Public ContactBruna Teixeira

Faculdade de Medicina da Universidade de São Paulo

brunabariani@yahoo.com.br+55(11)26618159

Outcome results

None listed

Source: REBEC (via WHO ICTRP)