Rapid Non-Invasive Brain Stimulation for Hoarding Disorder
TMS-HOLA
1 other identifier
interventional
10
1 country
1
Brief Summary
This study explores whether rapid non-invasive brain stimulation can help reduce hoarding disorder symptoms.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 27, 2024
CompletedFirst Posted
Study publicly available on registry
December 2, 2024
CompletedStudy Start
First participant enrolled
March 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2028
April 22, 2026
April 1, 2026
1.8 years
November 27, 2024
April 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Compulsive Acquisition Scale (CAS)
The Compulsive Acquisition Scale (CAS) is an 18-item questionnaire that measures the extent to which individuals acquire and feel compelled to acquire possessions. The total score (sum of 18 items) ranges from 0 to 126. Total score higher than 48 shows significant difficulty with acquiring.
Change from baseline to 3 weeks after treatment starts
Other Outcomes (1)
Change in Hoarding Symptom Severity as Measured by Saving Inventory-Revised (SI-R)
Change from baseline to 3 weeks after treatment starts
Study Arms (1)
Theta-burst stimulation (TBS)
EXPERIMENTALTheta-burst stimulation (a form of transcranial magnetic stimulation) targeting the right frontal pole.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Age 18-70 years
- Primary diagnosis of hoarding disorder
- Sufficient severity of hoarding symptoms
- Willing and able to understand and complete consent and study procedures
You may not qualify if:
- Psychiatric or medical conditions or medications that make participation unsafe
- Pregnant or nursing females
- Previous exposure to TMS or ECT
- History of any implanted device or psychosurgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Stanford University Medical Center
Palo Alto, California, 94305, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Carolyn I Rodriguez, MD, PhD
Stanford University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
November 27, 2024
First Posted
December 2, 2024
Study Start
March 27, 2026
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
January 1, 2028
Last Updated
April 22, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share