ClinicalTrials.gg
CompletedNCT02040805Updated Feb 11, 2020Results posted

Comparison of Treatment for Hoarding Disorder

An interventional study of Group Cognitive Behavioral Therapy and Peer Facilitated Support Group in Hoarding Disorder, sponsored by University of California, San Francisco. Completed at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-02-11.

Sponsored by University of California, San Francisco · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
323
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

Read the detailed description

The study design for this proposal is a stratified, randomized, single-blind, non- inferiority trial comparing the current standard of care for treatment of Hoarding Disorder (HD), Group Cognitive Behavioral Therapy (G-CBT), to an innovative and promising community-based treatment, Group Buried in Treasures (G-BiT). Participants will be stratified by gender, psychiatric status (high vs. low burden of psychiatric symptoms) and insurance status (insured vs. under- or un-insured) so that equal numbers of individuals with each of these characteristics are randomized to each treatment arm. They will then be randomly assigned (randomized) to either G-CBT or G-BiT. Participants will know which treatment group they are assigned to, but those members of the research team who are conducting clinical or neuropsychological assessments or analyzing the data will not; they will be blinded to participant group assignment, and group leaders will be blinded to the psychiatric status, neurocognitive status, insurance status, etc, of participants. The study is a non-inferiority trial, that is, the hypothesis to be tested is that G-BiT is as effective, or no less effective, than G-CBT. We chose a non-inferiority design because we have no reason to believe G-BiT is better than G-CBT and our preliminary data, as well as outcomes previously reported for G- CBT and G-BiT, suggest that these treatments may have similar efficacies.

02

Conditions studied

  • Hoarding Disorder

Keywords

  • compulsive hoarding
  • clutter
  • hoarding disorder
03

In context

Hoarding Disorder

32 studies on the registry are indexed under Hoarding Disorder; 5 are open to participants now.

This study's enrollment of 323 is above the median of 37 across 28 interventional studies indexed under Hoarding Disorder.

Browse Hoarding Disorder studies →

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,169 studies on the registry; 372 are open to participants now.

Of its 267 completed or terminated interventional studies of FDA-regulated products, 202 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Diagnosis of Hoarding Disorder

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
323 participants (actual)

Study arms

  • Experimental
    Group Cognitive-Behavioral Therapy

    Sixteen sessions of group therapy facilitated by a psychologist.

    Behavioral: Group Cognitive Behavioral Therapy

  • Experimental
    Peer Facilitated Support Group

    Fifteen sessions of peer-facilitated group support.

    Behavioral: Peer Facilitated Support Group

Interventions

  • BehavioralGroup Cognitive Behavioral Therapy

    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.

  • BehavioralPeer Facilitated Support Group

    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.

06

What researchers measure

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.

    Time frame: 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)

    The ADL-H is a 15-item self-report questionnaire that measures hoarding specific difficulties or problems that may impact daily functioning. It includes questions on activities affected by clutter or hoarding, problems in the home, and safety issues. For this study, the score on each ADL-H item was summed to create a total score ranging from 0 to 75. Higher scores indicate more severe functional impairment due to hoarding.

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

07

Results

Posted Feb 11, 2020
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.

Participant flow

Recruitment occurred during April 2014 through February 2016. Participants were individuals with Hoarding Disorder recruited primarily through the Mental Health Association - San Francisco and flyers in the bay area (e.g. community center boards, coffee shops, laundry mats, libraries).

Participant flow — Overall Study
MilestoneGroup Cognitive-Behavioral TherapyPeer Facilitated Support Group
Started160163
Completed118113
Not completed4250
Withdrew: Lost to follow-up149
Withdrew: Withdrawal by subject2841

Outcome measures

PrimarySaving 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.

Time frame:
Administered at screening before start of treatment groups and after last treatment group (20 weeks later).
Reported as:
Mean · units on a scale
Saving Inventory-Revised (SI-R)
units on a scaleGroup Cognitive-Behavioral TherapyPeer Facilitated Support Group
Baseline64.5 ± 11.766.4 ± 11.6
End of Treatment: 20 weeks later45.9 ± 15.047.8 ± 14.2
Statistical analysis
  • Group Cognitive-Behavioral Therapy vs Peer Facilitated Support Group · t-test, 1 sided · p = 0.04
SecondaryActivities of Daily Living Scale, Hoarding (ADL-H)

The ADL-H is a 15-item self-report questionnaire that measures hoarding specific difficulties or problems that may impact daily functioning. It includes questions on activities affected by clutter or hoarding, problems in the home, and safety issues. For this study, the score on each ADL-H item was summed to create a total score ranging from 0 to 75. Higher scores indicate more severe functional impairment due to hoarding.

Time frame:
Administered at baseline and after last treatment group (20 weeks later).
Reported as:
Mean · units on a scale
Activities of Daily Living Scale, Hoarding (ADL-H)
units on a scaleGroup Cognitive-Behavioral TherapyPeer Facilitated Support Group
Baseline29.9 ± 9.532.0 ± 11.2
End of Treatment: 20 weeks later25.5 ± 10.126.1 ± 8.7
Statistical analysis
  • Group Cognitive-Behavioral Therapy vs Peer Facilitated Support Group · t-test, 1 sided · p = 0.05
Post-hocLongitudinal Follow-Up: 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. Using the SI-R, we obtained longitudinal follow-up data (defined as a second post-treatment assessment of hoarding symptom severity at least three months following completion of treatment). The total SI-R score was used, which ranges from 0-92, higher scores indicating more severe hoarding.

Time frame:
The post-hoc longitudinal data were collected at varying time points, but at least three months after the treatment ended. The range was 3 months to 25 months, with a mean of 14 months after treatment end.
Reported as:
Mean · units on a scale
Longitudinal Follow-Up: Saving Inventory-Revised (SI-R)
units on a scaleGroup Cognitive-Behavioral TherapyPeer Facilitated Support Group
Longitudinal Follow-Up: Saving Inventory-Revised (SI-R)48.2 ± 14.947.9 ± 13.9
Statistical analysis
  • Group Cognitive-Behavioral Therapy vs Peer Facilitated Support Group · Mixed Models Analysis · p = <0.0001df=1
Post-hocLongitudinal Follow-Up: Activities of Daily Living Scale, Hoarding (ADL-H)

The ADL-H is a 15-item self-report questionnaire that measures hoarding specific difficulties or problems that may impact daily functioning. It includes questions on activities affected by clutter or hoarding, problems in the home, and safety issues. Using the ADL-H, we obtained longitudinal follow-up data (defined as a second post-treatment assessment of hoarding specific difficulties or problems that may impact daily functioning at least three months following completion of treatment). For this study, a total score using the sum of all of the items was created, ranging from 0 to a total possible of 75. Higher scores indicate more severe impairment due to hoarding.

Time frame:
Post-hoc longitudinal analyses were conducted at three or more months' following the end of treatment. The range was 3-25 months, and the mean time to longitudinal follow up was 14 months.
Reported as:
Mean · units on a scale
Longitudinal Follow-Up: Activities of Daily Living Scale, Hoarding (ADL-H)
units on a scaleGroup Cognitive-Behavioral TherapyPeer Facilitated Support Group
Longitudinal Follow-Up: Activities of Daily Living Scale, Hoarding (ADL-H)27.6 ± 11.627.8 ± 9.7
Statistical analysis
  • Group Cognitive-Behavioral Therapy vs Peer Facilitated Support Group · Mixed Models Analysis · p = <0.0001df=1

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Group Cognitive-Behavioral Therapy0/160 (0%)0/160 (0%)1/160 (0.6%)
Peer Facilitated Support Group0/163 (0%)0/163 (0%)2/163 (1.2%)
Most frequent other events
Most frequent other events
EventGroup Cognitive-Behavioral TherapyPeer Facilitated Support Group
Voluntary hospitalization due to "alcohol detox" "possible suicidality"Psychiatric disorders1/1600/163
SuicidalityPsychiatric disorders0/1601/163
Participant FellSocial circumstances0/1601/163

Baseline characteristics

Age, Continuous
Age, Continuous(years)Group Cognitive-Behavioral TherapyPeer Facilitated Support GroupTotal
Mean59.0 ± 10.958.9 ± 10.659.0 ± 10.7
Sex: Female, Male
Sex: Female, Male(Participants)Group Cognitive-Behavioral TherapyPeer Facilitated Support GroupTotal
Female117124241
Male433982
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Group Cognitive-Behavioral TherapyPeer Facilitated Support GroupTotal
Race/Ethnicity Characteristics — American Indian/Alaskan Native011
Race/Ethnicity Characteristics — Asian161733
Race/Ethnicity Characteristics — Black/African American17623
Race/Ethnicity Characteristics — Hispanic9817
Race/Ethnicity Characteristics — Native Hawaiian/Other Pacific Islander213
Race/Ethnicity Characteristics — Other or Multiracial232346
Race/Ethnicity Characteristics — White89101190
Race/Ethnicity Characteristics — Prefer not to answer459
08

Study locations

2 sites
  • Mental Health Association
    San Francisco, California 94102, United States
  • University of California, San Francisco
    San Francisco, California 94143, United States
09

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT02040805
Collaborators
Patient-Centered Outcomes Research Institute
Responsible party
Sponsor
First posted
Jan 20, 2014
Start date
Feb 2014
Primary completion
Dec 31, 2016
Completion
Dec 31, 2016
Results posted
Feb 11, 2020
Last update
Feb 11, 2020

Study contacts

Carol A. Mathews, MD
principal investigator · University of Florida
Kevin L. Delucchi, PhD
principal investigator · University of California, San Francisco

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion