- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04894851
Contingency Management for Hoarding Disorder (HCM)
A Pilot Study of Contingency Management for Hoarding Disorder
Aim 1: To test the efficacy of contingency management for patients with hoarding disorder (HD).
Hypothesis 1. Participants completing CM will show significant pre- to post-treatment decreases in severity of hoarding symptoms and clinician-rated impairment, and significant increases in quality of life.
Exploratory analyses will examine whether effect sizes compare with those of prior trials of cognitive-behavioral therapy (CBT) for HD conducted within our clinic, whether problem severity at follow-up is predicted by hoarding severity measured immediately after treatment completion, and whether readiness for change improves with treatment.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Connecticut
-
Hartford, Connecticut, United States, 06106
- Anxiety Disorders Center, Institute of Lilving
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosed with Primary Hoarding Disorder,
- currently participating in the Hoarding Disorder treatment group at the HH Anxiety Disorders Center
Exclusion Criteria:
- Not clinically appropriate for a group treatment format (i.e., active suicidality or aggressive behavior, psychosis, current physiological substance dependence, or personality issues that would be expected to substantially interfere with the group milieu; cognitively intact).
- Participants will also be excluded if they have previously completed CBT for HD.
- In addition, participants in the CM portion of the treatment will be required to live within one hour travel time of the treatment facility to allow for home visits with the independent rater.
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: Contingency Management
Receives contingency payments each month based on decluttering scores
|
Participants in the current study will receive contingencies for improvement in clutter, as measured by a trained, independent in-home rater.
Ratings will be completed by after study consent, and once every month thereafter, being conducted at weeks 0, 4, 8, 12, and 16 of treatment.
Participants will be reimbursed for each new 1-point reduction in CIR score, a set dollar amount per month for each CIR point reduction they maintain from baseline.
Therefore, a perfectly performing patient would earn reimbursement (A CIR reduction of 8 points made in the first month and maintained throughout treatment.
If a CIR score is higher than the prior month, the reinforcement schedule will reset to zero.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hoarding Rating Scale (HRS)
Time Frame: Change from week 1 (pre) to week 16 (post)
|
A brief 5-item interview to rate clutter, difficulty discarding, acquisition, distress, and impairment.
Each item is rated on a likert scale from 1 to 8, with higher scores reflective of higher symptom severity.
|
Change from week 1 (pre) to week 16 (post)
|
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Clutter Image Rating Scale
Time Frame: Change from week 1 (pre) to week 16 (post)
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A pictorial measure of clutter severity containing nine photographs depicting increasing levels of clutter.
CIR Scores can range from 1 to 9, with picture 1 indicating an absence of clutter and 9 indicative of the highest level of clutter.
Each available room will be rated.
|
Change from week 1 (pre) to week 16 (post)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Readiness Ruler
Time Frame: Change from week 1 (pre) to week 16 (post)
|
The Readiness Ruler is a brief measure of motivation, which prompts patients with a 10-point likert scale on which they rate readiness, with a score of 0 reflecting "not ready," and a score of 10 reflecting "ready."
The Readiness Ruler used in the current study will have patients rate both readiness for treatment and readiness for change.
|
Change from week 1 (pre) to week 16 (post)
|
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The World Health Organization Quality of Life Scale (WHOQOL-BREF)
Time Frame: Change from week 1 (pre) to week 16 (post)
|
Was developed by the World Health Organization and field-tested in 18 countries (including the United States) and contains 26 self-report questions, which measure the following broad domains: physical health, psychological health, social relationships, and environment.
These four scales can be summed to calculate a total quality of life (QOL) score, ranging from 0 (least favorable health status)to 100 (most favorable health status).
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Change from week 1 (pre) to week 16 (post)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Blaise l Worden, Ph.D., Hartford Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- WORD004040HI
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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Florida State UniversityCompleted
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New York State Psychiatric InstituteCompleted
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