Skip to content

Contingency Management for Hoarding Disorder

A Pilot Study of Contingency Management for Hoarding Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04894851
Acronym
HCM
Enrollment
13
Registered
2021-05-20
Start date
2013-08-31
Completion date
2014-10-31
Last updated
2021-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hoarding Disorder

Keywords

Hoarding Disorder, Contingency Management, Cognitive-Behavioral Therapy, Group Therapy

Brief summary

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.

Detailed description

The primary aim of the current study is a preliminary investigation of the efficacy of contingency management (CM) in the treatment of hoarding disorder (HD). CM is a highly efficacious treatment that has been used to treat issues such as substance use disorders, medication/ medical regimen nonadherence, and schizophrenia. While the current best-practice treatment for HD (cognitive behavioral therapy; CBT) is efficacious in that it results in significant symptom reduction, many patients continue to have high levels of functional impairment and distressing symptoms after treatment completion. We strongly feel that CM is able to address many of the issues that arise in the context of CBT for hoarding and we feel that the addition of CM to as CBT will result in significant pre- to post-treatment decreases in severity of hoarding symptoms and impairment, and significant increases in quality of life.

Interventions

BEHAVIORALContingency Management

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.

Sponsors

Hartford Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Hoarding Rating Scale (HRS)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.
Clutter Image Rating ScaleChange from week 1 (pre) to week 16 (post)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.

Secondary

MeasureTime frameDescription
Readiness RulerChange 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.
The World Health Organization Quality of Life Scale (WHOQOL-BREF)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).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026