Repetitive Transcranial Magnetic Stimulation (rTMS) in Depression

Northside Clinic, Australia

Status and phase: Terminated; Phase 4

Conditions: Depression

Treatments: Device: rTMS 5 x weekly; Device: rTMS 3 times weekly

Study type: Interventional

Funder types: Other

Identifiers

NCT00920322

UNSW HREC 9074

NSG HREC 153

Details and patient eligibility

About

This study will report on the outcomes of rTMS administered 3 times per week, compared with the standard protocol of 5 times per week. Participants will be randomly assigned to frequency condition and depressive symptomatology will be measured weekly using a range of clinician and self-rated questionnaires. Participants will remain in the study for at least 4 weeks, with the option of continuing for a further 2 weeks as judged by the study psychiatrist. It is hypothesised that rTMS administered three times per week will be equally as effective as rTMS administered five times per week in reducing depressive symptomatology.

Full description

Numerous studies have demonstrated the efficacy of active rTMS over sham rTMS for depression; however, few have systematically studied the optimal frequency of treatment sessions to achieve this efficacy. To date, the majority of studies have administered rTMS every weekday, although this approach has not been widely contested. In addition, most studies have only assessed the effectiveness of rTMS over a two week period, which has resulted in some improvement in depressive symptomatology; however, a longer treatment course would likely result in greater improvement. In this study depressed patients will be randomly assigned to receive rTMS either 3 or 5 times per week, for a period of 4-6 weeks. A range of rating scales will be used to assess the improvement of depressive symptomatology within and between the two frequency groups, to ultimately determine whether TMS is needed 5 times per week to achieve adequate anti-depressant effects or whether 3 times per week is sufficient in achieving a similar level of efficacy for patients.

Enrollment: 40 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Aged >/= 18
• DSM-IV diagnosis of Major Depressive Episode (bipolar or MDD)
• MADRS score >/= 20
• Able to give informed consent
• Psychoactive medication dosages have been stable for a period of 4 weeks prior to entry in the study

Exclusion criteria

• Co-morbid alcohol or drug abuse or dependence (last 3 months), current eating disorder, mental retardation, schizophrenia, rapid cycling bipolar
• A history of mood 'switching' in response to other treatments, which cannot be contained by concurrent treatment, e.g., mood stabiliser
• Pregnancy
• Significant neurological disorder that increases seizure risk
• Metal objects in the head, pacemakers, or a history of epilepsy
• Patients who have failed to respond to a course of ECT in their current episode of depression
• A high risk of suicide

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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40 participants in 2 patient groups

five times weekly

Active Comparator group

Description:

Patients will receive rTMS on each weekday for 4 weeks (5 x weekly)

Treatment:

Device: rTMS 5 x weekly

three times weekly

Experimental group

Description:

Patients will receive rTMS three times weekly for four weeks

Treatment:

Device: rTMS 3 times weekly