Contingency Management for Hoarding Disorder
Completed · Not applicable
Conditions studied: Hoarding Disorder
In brief
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.
Key facts
- Study ID
- NCT04894851
- Run by
- Hartford Hospital
- People needed
- 13
- Starts
- 2013-08-01
- Expected to finish
- 2014-10-01
- Last updated by the study team
- 2021-05-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosed with Primary Hoarding Disorder,
- currently participating in the Hoarding Disorder treatment group at the HH Anxiety Disorders Center
You may not qualify if…
- 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.
Where it is running
- Anxiety Disorders Center, Institute of Lilving — Hartford, Connecticut, United States
Full record on ClinicalTrials.gov
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