NCT02843308

Brief Summary

The proposed study aims to investigate the efficacy of adding in-home decluttering practice to Buried in Treasures Workshop (BIT) facilitated group treatment for hoarding disorder.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
41

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2016

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

July 20, 2016

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 25, 2016

Completed
1 month until next milestone

Study Start

First participant enrolled

September 1, 2016

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2019

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 2, 2020

Completed
5.6 years until next milestone

Results Posted

Study results publicly available

November 21, 2025

Completed
Last Updated

November 21, 2025

Status Verified

November 1, 2025

Enrollment Period

2.8 years

First QC Date

July 20, 2016

Results QC Date

September 30, 2025

Last Update Submit

November 11, 2025

Conditions

Keywords

hoarding disorderhoardingclutter

Outcome Measures

Primary Outcomes (1)

  • Number of Patients Who Met and Exceeded Response Criteria of the Saving Inventory-Revised (SI-R)

    The SI-R is a 23-item questionnaire with 3 sub-scales for difficulty discarding, excessive clutter, and compulsive acquisition. The total score ranges from 0 to 92. The greater the score, the more severe the hoarding symptoms. Total score higher than 41 shows significant difficulty with clutter. For the acquisition subscale, items 2 (reverse score), 9, 11, 14, 16, 18 and 21 are summed together. The subscale ranges from 0 to 28 and score greater than 13 indicates difficulty with excessive acquisition. For the difficulty discarding subscale, items 4(reverse score), 6, 7, 13, 17, 19, 23 are summed together. The subscale ranges from 0 to 28 and score greater than 13 indicates difficulty with discarding. For the clutter subscale, items 1, 3, 5, 8, 10, 12, 15, 20, 22 are summed together. The subscale ranges from 0 to 36 and score greater than 15 indicates difficulty with accumulated clutter. Response was defined as at least a 14 point change (pre-post) in the total score.

    Change from baseline (pre-treatment) to week 18 (post-treatment) the Immediate Treatment Arm/Group and change from baseline (pre-treatment at 18 weeks) to 36 weeks (post-treatment) for the Delayed Treatment Arm/Group

Study Arms (2)

Immediate Treatment

EXPERIMENTAL

Facilitated group therapy with behavioral practice; 18 weeks

Behavioral: Facilitated group therapy with behavioral practice; 18 weeks

Delayed Treatment

EXPERIMENTAL

Facilitated group therapy with behavioral practice; 18 weeks (after a 18-20 week delay)

Behavioral: Facilitated group therapy with behavioral practice; 18 weeks

Interventions

Facilitated group therapy for hoarding disorder with behavioral practice

Delayed TreatmentImmediate Treatment

Eligibility Criteria

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

You may qualify if:

  • Age 18 to 70 years
  • Either gender and all ethno-racial groups
  • Physically healthy male or non-pregnant female.
  • Hoarding Disorder primary condition
  • Willing and able to understand and complete consent and study procedures
  • English speaking

You may not qualify if:

  • Current or past history of bipolar, psychotic or eating disorders, substance dependence, or substance abuse in the last year.
  • Clinically at risk of suicide with Columbia Suicide Severity Rating Scale (C-SSRS) Suicidal Ideation Subscale of 4 or higher (i.e. suicidal intent without specific plan)
  • Major medical or neurological conditions that increase the risk of participation or that would prevent completing assigned behavioral practice tasks.
  • Unable or unwilling to allow study staff into home for home assessment
  • Currently at high risk for eviction
  • Animal hoarding or squalor

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Stanford, California, 94305, United States

Location

Related Publications (1)

  • Wheaton MG, Varias AD, Sandhu T, Munoz Rodriguez PA, Mukunda P, Filippou-Frye M, Millen A, Lombardi A, van Roessel P, Raila H, Anderson K, Linkovski O, Mahnke A, Sanchez C, McCarthy E, Wright B, Mibenge C, Rico Y, Righi S, Halsey C, Torio L, Asgari S, Qiu T, Garcia G, Jo B, Belofsky B, Shuer LJ, Frost RO, Rodriguez CI. Randomized waitlist-controlled trial of buried in treasures facilitated support groups and in-home uncluttering (BIT+) for hoarding disorder. J Psychiatr Res. 2024 Aug;176:58-67. doi: 10.1016/j.jpsychires.2024.05.055. Epub 2024 May 30.

    PMID: 38843580BACKGROUND

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

Limitations and Caveats

Several limitations deserve consideration (see paper Wheaton et al., 2024). Although this is the first trial of BIT+ to include a control group, the group was limited to waiting list (which controlled for the passage of time) and did not include another credible treatment comparator. As a result, other potential confounding variables such as placebo effects and attention from the research team were not controlled.

Results Point of Contact

Title
Carolyn Rodriguez, MD, PhD
Organization
Stanford University School of Medicine

Study Officials

  • Carolyn Rodriguez, M.D., Ph.D.

    Stanford University

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 20, 2016

First Posted

July 25, 2016

Study Start

September 1, 2016

Primary Completion

June 30, 2019

Study Completion

April 2, 2020

Last Updated

November 21, 2025

Results First Posted

November 21, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations