NCT02040805

Brief Summary

This study proposes to compare two forms of treatment for Hoarding Disorder (HD), a common and impairing neuropsychiatric syndrome that has a profound impact on the lives and functioning of individuals, families, and society. Specifically, we will compare a novel community-based group treatment led by individuals from the community who are not mental health professionals to the current standard of care treatment for Hoarding Disorder, Cognitive Behavioral Therapy, conducted by psychologists in a group setting. We hypothesized that both treatment types will be similarly effective in reducing hoarding severity.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
323

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2014

Typical duration for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

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

January 16, 2014

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 20, 2014

Completed
12 days until next milestone

Study Start

First participant enrolled

February 1, 2014

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2016

Completed
3.1 years until next milestone

Results Posted

Study results publicly available

February 11, 2020

Completed
Last Updated

February 11, 2020

Status Verified

February 1, 2020

Enrollment Period

2.9 years

First QC Date

January 16, 2014

Results QC Date

June 9, 2017

Last Update Submit

February 4, 2020

Conditions

Keywords

compulsive hoardingclutterhoarding disorder

Outcome Measures

Primary Outcomes (1)

  • Saving Inventory-Revised (SI-R)

    This is a 23-item self-report questionnaire that measures hoarding symptoms and their impact, including problems with acquisition, clutter, and difficulty discarding, as well as distress and impairment/interference. The SI-R is scored on a scale of 0-92. Higher scores indicate more severe hoarding, and scores of 42 and over are considered clinically significant hoarding. Although subscale scores can be calculated, this study uses total scores as the primary outcome.

    Administered at screening before start of treatment groups and after last treatment group (20 weeks later).

Secondary Outcomes (1)

  • Activities of Daily Living Scale, Hoarding (ADL-H)

    Administered at baseline and after last treatment group (20 weeks later).

Study Arms (2)

Group Cognitive-Behavioral Therapy

EXPERIMENTAL

Sixteen sessions of group therapy facilitated by a psychologist.

Behavioral: Group Cognitive Behavioral Therapy

Peer Facilitated Support Group

EXPERIMENTAL

Fifteen sessions of peer-facilitated group support.

Behavioral: Peer Facilitated Support Group

Interventions

Group therapy over approximately 20 weeks, based on a structured manual adapted from the individual CBT workbook for hoarding by Steketee and Frost (2006). Each session will be 2 hours in length and consists of weekly check-ins, psychoeducation about hoarding, developing understanding and awareness of one's hoarding symptoms and patterns, behavior modification, cognitive restructuring, goal-setting, motivational enhancement, in vivo and imaginal exposure for discarding and acquisition, executive skills training (organization, sorting, planning, decision-making, problem-solving, etc.), guidelines on establishing "clutter buddies", and relapse prevention. Groups will be led by clinical postdoctoral psychology fellows in the Department of Psychiatry at UCSF.

Group Cognitive-Behavioral Therapy

Fifteen sessions of peer facilitated, group support, over the course of 20 weeks, based on a structured manualized approach (Buried in Treasures: Help for Compulsive Acquiring, Saving, and Hoarding). Each session will be 2 hours in length. In this model, two trained peers, usually, but not necessarily, with personal lived experience of hoarding, will guide the group chapter by chapter through the Buried in Treasures manual.

Peer Facilitated Support Group

Eligibility Criteria

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

You may qualify if:

  • Diagnosis of Hoarding Disorder

You may not qualify if:

  • Individuals with active psychosis, schizophrenia, intellectual disability, or known dementia will be excluded
  • Individuals who have participated in either cognitive-behavioral therapy for hoarding (group or individual) or in group Buried in Treasures in the past year

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Mental Health Association

San Francisco, California, 94102, United States

Location

University of California, San Francisco

San Francisco, California, 94143, United States

Location

MeSH Terms

Conditions

Hoarding DisorderSpeech Disorders

Condition Hierarchy (Ancestors)

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

Limitations and Caveats

The primary limitation in this study was loss to follow up. Additionally, the longitudinal follow-up assessment was post-hoc rather than being planned prior to study initiation.

Results Point of Contact

Title
Dr. Kevin L. Delucchi
Organization
University of California, San Francisco

Study Officials

  • Carol A. Mathews, MD

    University of Florida

    PRINCIPAL INVESTIGATOR
  • Kevin L. Delucchi, PhD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Two-arm parallel clinical trial with assessments pre- and post-treatment.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 16, 2014

First Posted

January 20, 2014

Study Start

February 1, 2014

Primary Completion

December 31, 2016

Study Completion

December 31, 2016

Last Updated

February 11, 2020

Results First Posted

February 11, 2020

Record last verified: 2020-02

Locations