Comparison of Treatment for Hoarding Disorder

Status Completed

Clinical Trial Summary

This study proposes to compare two forms of treatment for Hoarding Disorder (HD), a common and impairing neuropsychiatric syndrome that has a profound impact on the lives and functioning of individuals, families, and society. Specifically, we will compare a novel community-based group treatment led by individuals from the community who are not mental health professionals to the current standard of care treatment for Hoarding Disorder, Cognitive Behavioral Therapy, conducted by psychologists in a group setting. We hypothesized that both treatment types will be similarly effective in reducing hoarding severity.

Clinical Trial Description

The study design for this proposal is a stratified, randomized, single-blind, non- inferiority trial comparing the current standard of care for treatment of Hoarding Disorder (HD), Group Cognitive Behavioral Therapy (G-CBT), to an innovative and promising community-based treatment, Group Buried in Treasures (G-BiT). Participants will be stratified by gender, psychiatric status (high vs. low burden of psychiatric symptoms) and insurance status (insured vs. under- or un-insured) so that equal numbers of individuals with each of these characteristics are randomized to each treatment arm. They will then be randomly assigned (randomized) to either G-CBT or G-BiT. Participants will know which treatment group they are assigned to, but those members of the research team who are conducting clinical or neuropsychological assessments or analyzing the data will not; they will be blinded to participant group assignment, and group leaders will be blinded to the psychiatric status, neurocognitive status, insurance status, etc, of participants. The study is a non-inferiority trial, that is, the hypothesis to be tested is that G-BiT is as effective, or no less effective, than G-CBT. We chose a non-inferiority design because we have no reason to believe G-BiT is better than G-CBT and our preliminary data, as well as outcomes previously reported for G- CBT and G-BiT, suggest that these treatments may have similar efficacies. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02040805
Study type	Interventional
Source	University of California, San Francisco
Contact
Status	Completed
Phase	N/A
Start date	February 2014
Completion date	December 31, 2016

View Details

See also
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Completed	`NCT04270825` - Group Treatment for Hoarding Disorder	N/A
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Completed	`NCT01451697` - Cognitive Remediation for Neuropsychological Impairment in Compulsive Hoarding	Early Phase 1
Completed	`NCT03828461` - Hoarding Disorder Treatment With Virtual Reality	N/A
Recruiting	`NCT04712474` - In-home Decluttering Augmentation of Group CBT for HD	N/A
Completed	`NCT02367430` - Critical Time Intervention for Individuals With Hoarding Disorder	N/A
Active, not recruiting	`NCT03734705` - Imaginal Exposure for Hoarding Disorder	N/A
Not yet recruiting	`NCT03772301` - Evaluation of Hoarding Behaviour and Eating Disorders Among Holocaust Survivors and Their Descendants
Completed	`NCT02377986` - Augmenting Buried in Treasures Workshop (BIT) With In-home Decluttering Practice for Individuals With Hoarding Disorder	N/A
Completed	`NCT04239729` - Web-based Acceptance and Commitment Therapy for Hoarding Disorder	N/A
Recruiting	`NCT05985356` - Neuromodulation for Comorbid Hoarding Disorder and Depression	N/A
Completed	`NCT04894851` - Contingency Management for Hoarding Disorder	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.