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| ID | Type | Description | Link |
|---|---|---|---|
| R01MH063405 | U.S. NIH Grant/Contract | View source | |
| DATR A4-GPX |
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| Name | Class |
|---|---|
| National Institute of Mental Health (NIMH) | NIH |
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This 12-week study will evaluate the effectiveness of repetitive transcranial magnetic stimulation (rTMS) of the brain, followed by citalopram (Celexa®), for treatment of depression associated with small vascular lesions in the brain (vascular depression).
Vascular depression is a condition that typically affects the elderly and is associated with small vascular lesions. It is more resistant to treatment and has a poorer outcome than nonvascular depression. By altering excitability in the cortical area of the brain, rTMS may be an effective treatment neuropsychiatric conditions, particularly depression.
Participants in this study will be randomly assigned to 15 treatments of either rTMS or sham rTMS for 3 weeks. Following treatment, participants will receive citalopram for 9 weeks. Response rates to treatment; relapse rates; the size, number, and location of the vascular lesions; and the amount of regional brain atrophy will be measured. Improvements in activities of daily living, quality of life, and cognitive function will also be also measured.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | Participants will receive treatment with repetitive transcranial magnetic stimulation and citalopram. |
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| 2 | Active Comparator | Participants will receive treatment with sham repetitive transcranial magnetic stimulation and citalopram. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Repetitive transcranial magnetic stimulation (rTMS) | Procedure | Participants will receive 15 treatments of rTMS over 3 weeks. |
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| Measure | Description | Time Frame |
|---|---|---|
| Response rates to treatment; relapse rates; the size, number, and location of the vascular lesions; and the amount of regional brain atrophy | Measured at Week 12 |
| Measure | Description | Time Frame |
|---|---|---|
| Improvements in activities of daily living, quality of life, and cognitive function | Measured at Week 12 |
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Inclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Iowa Health Care | Iowa City | Iowa | 52242-1087 | United States |
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| ID | Term |
|---|---|
| D003866 | Depressive Disorder |
| D003863 | Depression |
| ID | Term |
|---|---|
| D019964 | Mood Disorders |
| D001523 | Mental Disorders |
| D001526 | Behavioral Symptoms |
| D001519 | Behavior |
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| ID | Term |
|---|---|
| D050781 | Transcranial Magnetic Stimulation |
| D015283 | Citalopram |
| ID | Term |
|---|---|
| D055909 | Magnetic Field Therapy |
| D013812 | Therapeutics |
| D011437 | Propylamines |
| D000588 | Amines |
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| Citalopram | Drug | After completing treatment with rTMS or sham rTMS, participants will take citalopram for 9 weeks. |
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| Sham rTMS | Procedure | Participants will receive 15 treatments of sham rTMS over 3 weeks. |
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| D009930 |
| Organic Chemicals |
| D009570 | Nitriles |
| D001572 | Benzofurans |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |