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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02306174
Other study ID # 20140644
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 2014
Est. completion date August 2026

Study information

Verified date September 2023
Source University of Miami
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 200
Est. completion date August 2026
Est. primary completion date August 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive 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).

Locations

Country Name City State
United States University of Miami Coral Gables Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Miami

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hoarding Rating Scale Interview The 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.
22 weeks
Primary Clinician's Global Impression Improvement and Severity ratings The 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. 22 weeks
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