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Cognitive Rehabilitation and Exposure-based Class for Compulsive Hoarding

Cognitive Rehabilitation and Exposure-based Class for Compulsive Hoarding

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02306174
Enrollment
13
Registered
2014-12-03
Start date
2014-09-01
Completion date
2025-06-26
Last updated
2026-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hoarding Disorder

Keywords

Hoarding

Brief summary

The purpose of this protocol is to investigate the effectiveness of a manualized, 20-week group cognitive rehabilitation (CR) and exposure therapy (ET) course for compulsive hoarding. The overarching aim is to understand whether this course will decrease the core symptoms of hoarding and associated features.

Interventions

BEHAVIORALCognitive Rehabilitation and Exposure-based Class for Compulsive Hoarding

The group sessions consists of 20 classes, each lasting approximately 90 minutes and may consist of some or all of the following: * A group agreement and a confidentiality contract * Homework assignments * Viewing informational videos about hoarding * Behavioral experiments including sorting and discarding exercises * Non-acquisition exposures This course is based on the Manual Cognitive Rehabilitation and Exposure/Sorting Therapy for Compulsive Hoarding (Ayers et al., 2014).

Sponsors

University of Miami
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Include: * Individuals who exhibit subclinical and clinical levels of hoarding disorder, as determined by the SCID interview conducted at the screening assessment, will be eligible to participate in the study. Individuals may also display clinically relevant symptoms of hoarding as indicated by scores on the Hoarding Rating Scale Interview (HRS-I) and/or on the Saving Inventory-Revised (SIR). * Comorbid mood and anxiety disorders are permitted. * English-speaking * Pregnant women

Exclusion criteria

* Adults unable to consent * Individuals who are not yet adults (infants, children, teenagers) * Individuals who are over the age of 85 * Individuals with cognitive or physical impairments that would interfere with their participation (e.g., Dementia, uncorrected hearing) * Participants who have current or past psychotic symptoms or current or past alcohol/substance abuse/dependence may also be excluded. * Participants may also be excluded if they are currently in other forms of psychotherapy. * Participants may be excluded if they have had a change in psychotropic medications within three months of the baseline assessment/first class. * Participants may be excluded if hoarding is not their primary diagnosis. * Prisoners

Design outcomes

Primary

MeasureTime frameDescription
Hoarding Rating Scale Interview22 weeksThe Hoarding Rating scale has a total score ranging from 0 -40 with the higher score indicating higher symptoms of hoarding. This will be used to assess whether hoarding symptoms decrease as a result of treatment.
Clinician's Global Impression Improvement and Severity ratings22 weeksThe CGI has a score range of 0-7 with the higher score indicating more severe symptoms.This will be used to assess whether hoarding symptoms decrease as a result of treatment.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKiara Timpano, PhD

University of Miami

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 18, 2026