- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01585896
Self-Help Group for the Treatment of Hoarding Disorder
September 29, 2023 updated by: Kiara Timpano, University of Miami
The proposed study aims to investigate the efficacy of a facilitated self-help group for the treatment of hoarding disorder.
Eligible participants will take part in a facilitated self-help group.
The investigators aim to investigate the effects of a self-help group on hoarding symptoms.
The investigators hypothesize that participants will demonstrate decreased hoarding symptoms over time.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Savannah King
- Phone Number: 305-284-5394
- Email: pasolab@miami.edu
Study Locations
-
-
Florida
-
Coral Gables, Florida, United States, 33124
- University of Miami
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- clinically relevant symptoms of hoarding disorder
Exclusion Criteria:
- under 18
- psychotic disorders, bipolar disorder, substance abuse or dependence
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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: Self-help group
The facilitated self-help group, which represents an empirically supported intervention for hoarding (Frost et al., 2011).
|
The facilitated self-help group may last approximately 13 sessions.
This treatment represents an empirically supported intervention for hoarding (Frost et al., 2011), based on a Facilitator's Manual (Maxner et al., 2010), which is a treatment manual based on the book Buried in Treasures: Help for Compulsive Acquiring, Saving, and Hoarding (Tolin, Frost, & Steketee, 2007).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hoarding Rating Scale
Time Frame: 13 weeks
|
Interviewer-rated measure of hoarding severity will be administered at Screening, Pre-Treatment, Mid-Treatment (approximately Week 7), Post-Treatment (approximately week 13), 1-month Follow-up The Hoarding Rating scale has a total score ranging from 0-40 with the higher score indicating higher symptoms of hoarding.
|
13 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Kiara R Timpano, PhD, University of Miami
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2012
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
April 23, 2012
First Submitted That Met QC Criteria
April 24, 2012
First Posted (Estimated)
April 26, 2012
Study Record Updates
Last Update Posted (Actual)
October 3, 2023
Last Update Submitted That Met QC Criteria
September 29, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20111146
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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