- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02306174
Cognitive Rehabilitation and Exposure-based Class for Compulsive Hoarding
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Florida
-
Coral Gables, Florida, United States, 33146
- University of Miami
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Cognitive Rehabilitation and Exposure-based Class for Compulsi
Cognitive training is to improve thinking by learning new skills and strategies. The class begins with cognitive training to increase ability to carry out the skills learned later in treatment. Exposure therapy for discarding and acquiring helps to improve ability to make choices about possessions and learn to tolerate anxiety. Participants will face making difficult choices about items and potentially letting them go. Through repeated exposure to decisions about discarding and acquiring, distress about letting go or making choices about items will decrease over time. |
The group sessions consists of 20 classes, each lasting approximately 90 minutes and may consist of some or all of the following:
This course is based on the Manual Cognitive Rehabilitation and Exposure/Sorting Therapy for Compulsive Hoarding (Ayers et al., 2014). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hoarding Rating Scale Interview
Time Frame: 22 weeks
|
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
|
Clinician's Global Impression Improvement and Severity ratings
Time Frame: 22 weeks
|
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
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kiara Timpano, PhD, University of Miami
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20140644
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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