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Behavioral Intervention
Cognitive Rehabilitation for Hoarding Disorder
N/A
Waitlist Available
Led By Kiara Timpano, PhD
Research Sponsored by University of Miami
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Individuals who are over the age of 85
Individuals who are not yet adults (infants, children, teenagers)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 22 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial will test a manualized, 20-week group cognitive rehabilitation and exposure therapy course to see if it can decrease the core symptoms of hoarding and associated features.
Who is the study for?
This trial is for adults with hoarding disorder, as confirmed by specific interviews and questionnaires. They can have other mood or anxiety disorders and be pregnant. Exclusions include recent medication changes, other psychotherapies, primary diagnoses other than hoarding, cognitive impairments like dementia, substance abuse issues, prisoners, and those under 18 or over 85.
What is being tested?
The study tests a structured 20-week group class combining cognitive rehabilitation (CR) and exposure therapy (ET) to reduce symptoms of compulsive hoarding. The goal is to see if this course helps people manage their hoarding behavior better than before.
What are the potential side effects?
Since the intervention involves psychological therapy rather than medication, typical medical side effects are not expected. Participants may experience emotional discomfort during exposure therapy as they confront their hoarding behaviors.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am over 85 years old.
Select...
I am under 18 years old.
Select...
I do not have any cognitive or physical impairments that would prevent me from participating.
Select...
I am unable to give consent for myself.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 22 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~22 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Clinician's Global Impression Improvement and Severity ratings
Hoarding Rating Scale Interview
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Cognitive Rehabilitation and Exposure-based Class for CompulsiExperimental Treatment1 Intervention
Cognitive training is to improve thinking by learning new skills and strategies. The class begins with cognitive training to increase ability to carry out the skills learned later in treatment.
Exposure therapy for discarding and acquiring helps to improve ability to make choices about possessions and learn to tolerate anxiety. Participants will face making difficult choices about items and potentially letting them go. Through repeated exposure to decisions about discarding and acquiring, distress about letting go or making choices about items will decrease over time.
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Who is running the clinical trial?
University of MiamiLead Sponsor
949 Previous Clinical Trials
428,264 Total Patients Enrolled
2 Trials studying Hoarding Disorder
82 Patients Enrolled for Hoarding Disorder
Kiara Timpano, PhDPrincipal InvestigatorUniversity of Miami
1 Previous Clinical Trials
50 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am over 85 years old.I am unable to give consent for myself.I am under 18 years old.I do not have any cognitive or physical impairments that would prevent me from participating.I haven't changed my mental health medications in the last 3 months.
Research Study Groups:
This trial has the following groups:- Group 1: Cognitive Rehabilitation and Exposure-based Class for Compulsi
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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