Group Treatment for Hoarding Disorder
1 other identifier
interventional
8
1 country
1
Brief Summary
This study assesses the effectiveness of a novel group treatment for hoarding disorder.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2019
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 25, 2019
CompletedStudy Start
First participant enrolled
October 1, 2019
CompletedFirst Posted
Study publicly available on registry
February 17, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
May 31, 2020
CompletedFebruary 10, 2021
February 1, 2021
8 months
March 25, 2019
February 7, 2021
Conditions
Outcome Measures
Primary Outcomes (4)
Changes in Hoarding Rating Scale (HRS)
The Hoarding Rating Scale is a commonly used measure of hoarding symptoms in which participants rate the severity of their symptoms. Minimum score is 0 and maximum score is 40. Higher scores indicate more severe/worse symptoms.
Baseline, 10 weeks, 20 weeks, 24 weeks
Changes in Reciprocal Attachment Questionnaire Adapted (RAQ-A)
The Reciprocal Attachment Questionnaire Adapted assesses attachment to one's belongings, with higher scores indicating greater attachment to possessions (i.e., worse outcome). Minimum score is 75 and maximum score is 375.
Baseline, 10 weeks, 20 weeks, 24 weeks
Changes in Adult Attachment Scale (AAS)
The AAS is a measure of two dimensions proposed to underlie interpersonal attachment security: anxiety and avoidance. Higher scores indicate worse outcomes. Minimum score is 0 and maximum score is 72.
Baseline, 10 weeks, 20 weeks, 24 weeks
Changes in Interpersonal Needs Questionnaire (INQ)
The INQ is a measure of two interpersonal risk factors, namely perceived burdensomeness and thwarted belongingness, with higher scores indicating higher levels of each construct (i.e., worse outcome). Minimum score is 15 and maximum score is 105.
Baseline, 10 weeks, 20 weeks, 24 weeks
Study Arms (1)
CBT with IPT
EXPERIMENTALGroup CBT with IPT will consist of 20 weekly two-hour sessions and has been developed for the proposed study based on the protocols for group CBT for HD and group IPT. Treatment includes strategies from CBT, including cognitive restructuring, behavioral exposures, and organizational strategies, as well as strategies from IPT, including role-play, interpersonal skills building, communication analysis, and decision analysis.
Interventions
Group treatment designed to target relationships with both possessions and people.
Eligibility Criteria
You may qualify if:
- Clinical diagnosis of HD
You may not qualify if:
- Evidence of a severe mental illness or substance use disorder that would impede the completion of the treatment
- Current receipt of CBT for HD
- Initiation of new psychotropic medications for symptoms of HD
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Florida State University
Tallahassee, Florida, 32304, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Graduate Student
Study Record Dates
First Submitted
March 25, 2019
First Posted
February 17, 2020
Study Start
October 1, 2019
Primary Completion
May 31, 2020
Study Completion
May 31, 2020
Last Updated
February 10, 2021
Record last verified: 2021-02
Data Sharing
- IPD Sharing
- Will not share
Data will not be shared.