N/A
N=14
Critical Time Intervention for Individuals With Hoarding Disorder
Hoarding Disorder
Bottom Line
View on ClinicalTrials.gov: NCT02367430 ↗Enrolled (actual)
14
Serious AEs
0.0%
Results posted
Feb 2020
Primary outcome: Primary: Savings Inventory-Revised — 67.5; 57.2; 54.8; 51.3 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Critical Time Intervention With Buried in Treasures included (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- New York State Psychiatric Institute
- Primary completion
- Jul 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Savings Inventory-Revised |
67.5; 57.2; 54.8; 51.3 | — |
| PRIMARY Clutter Image Rating Scale |
6; 5; 5; 5 | — |
Summary
The purpose of this study is to investigate whether a well-established case management model called Critical Time Intervention (CTI) can help individuals with hoarding disorder who are concerned about the risk of eviction. Each individual with hoarding disorder will be assigned to work with a CTI Specialist for 9 months, who will provide referrals for mental health treatment, legal consultations, and registration for entitlements. All participants will be offered a facilitated group intervention called the Buried in Treasures Workshop. The CTI Specialist will also facilitate reconnecting the individual with supportive family/friends and will monitor and support the de-cluttering of the patient's home.
Eligibility Criteria
Inclusion Criteria
- primary Hoarding Disorder
- age 18 or over
- Individuals concerned with the threat of eviction due to clutter
- Patient must be physically healthy
- Willing and able to understand and complete consent procedure
- English speaking
Exclusion Criteria
- Not primary Hoarding Disorder
- Severly depressed patients; Hamilton depression rating scale greater than 30 or judged clinically to be at risk of suicide with Columbia Suicide Severity Rating Scale
Data sourced from ClinicalTrials.gov (NCT02367430). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.