NCT06712914

Brief Summary

This study explores whether rapid non-invasive brain stimulation can help reduce hoarding disorder symptoms.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
21mo left

Started Mar 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress6%
Mar 2026Jan 2028

First Submitted

Initial submission to the registry

November 27, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 2, 2024

Completed
1.3 years until next milestone

Study Start

First participant enrolled

March 27, 2026

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2028

Last Updated

April 22, 2026

Status Verified

April 1, 2026

Enrollment Period

1.8 years

First QC Date

November 27, 2024

Last Update Submit

April 21, 2026

Conditions

Keywords

TMShoarding disorderhoardingclutteriTBS

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)

EXPERIMENTAL

Theta-burst stimulation (a form of transcranial magnetic stimulation) targeting the right frontal pole.

Device: MagPro X100 by MagVenture

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.

Theta-burst stimulation (TBS)

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

Related Links

MeSH Terms

Conditions

Hoarding DisorderHoardingSpeech Disorders

Condition Hierarchy (Ancestors)

Obsessive-Compulsive DisorderAnxiety DisordersMental DisordersBehaviorLanguage DisordersCommunication DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Carolyn I Rodriguez, MD, PhD

    Stanford University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Paula Munoz Rodriguez, PhD

CONTACT

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

Locations