RECRUITINGINTERVENTIONAL
Rapid Non-Invasive Brain Stimulation for Hoarding Disorder
About This Trial
This study explores whether rapid non-invasive brain stimulation can help reduce hoarding disorder symptoms.
Who May Be Eligible (Plain English)
Who May Qualify:
1. Age 18-70 years
2. Primary diagnosis of hoarding disorder
3. Sufficient severity of hoarding symptoms
4. Willing and able to understand and complete consent and study procedures
Who Should NOT Join This Trial:
1. Psychiatric or medical conditions or medications that make participation unsafe
2. Pregnant or nursing females
3. Previous exposure to TMS or ECT
4. History of any implanted device or psychosurgery
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
1. Age 18-70 years
2. Primary diagnosis of hoarding disorder
3. Sufficient severity of hoarding symptoms
4. Willing and able to understand and complete consent and study procedures
Exclusion Criteria:
1. Psychiatric or medical conditions or medications that make participation unsafe
2. Pregnant or nursing females
3. Previous exposure to TMS or ECT
4. History of any implanted device or psychosurgery
Treatments Being Tested
DEVICE
MagPro X100 by MagVenture
Participants will receive 5 session per day of TBS for 6 days (30 sessions total). Six treatment days have to occur within a 2 week period. Each session will be comprised of 1800 pulses, using a MagVenture MagPro X100.
Locations (1)
Stanford University Medical Center
Palo Alto, California, United States