- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00073346
Pilot Trial of Cognitive and Behavioral Treatment of Compulsive Hoarding Compared to Wait List Control
Cognitive and Behavioral Treatment of Compulsive Hoarding
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Compulsive hoarding is characterized by excessive acquisition of possessions, difficulty discarding possessions, and excessive clutter. This condition is resistant to standard pharmacological and psychotherapeutic interventions that have proven effective in treating other obsessive compulsive spectrum disorders. This study aimed to determine the effectiveness of a specialized cognitive behavioral therapy (CBT) designed for treating hoarding symptoms.
This study consists of three phases. In Phase 1, pilot data from previous studies were examined to develop an intervention suitable for use in a waitlist trial. In Phase 2, pilot study information were used to develop and test a treatment manual for compulsive hoarding. During this phase, treatment was applied flexibly to allow for variations in treatment duration and choice of techniques. During Phase 3, participants were randomly assigned to 26 weekly sessions of CBT or to a 12-week wait-list control, followed by active treatment for a fixed duration of 26 sessions. Therapist adherence and competence were assessed through audiotaped therapy sessions.
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
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Connecticut
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Hartford, Connecticut, United States, 06106
- Hartford Hospital, Institute of Living
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Massachusetts
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Boston, Massachusetts, United States, 02215
- BostonUCRC
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
- Display at least moderately severe hoarding symptoms
- Must live within 45 minutes of Boston, MA or Hartford, CT
Exclusion criteria:
- Ten or more sessions of cognitive behavior therapy for hoarding
- Concurrent psychotherapy or medications
- Suicidal, psychotic, or other psychiatric symptoms requiring hospitalization
- Compulsive buying symptoms that are part of a manic phase of bipolar disorder
- Mental retardation, dementia, brain damage, or other cognitive dysfunction that would interfere with the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: cognitive behavior therapy for hoarding disorder
Cognitive behavior therapy included 26 sessions of motivational enhancements; skills training for sorting, organizing and problem solving; direct practice not acquiring new items and discarding possessions to remove clutter and organize possessions; cognitive therapy to evaluate beliefs about possessions; and relapse prevention skills.
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NO_INTERVENTION: Wait list control
Participants waited to receive treatment for 12 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Saving Inventory-Revised
Time Frame: change from baseline to week 12; change from baseline to week 26
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Self-report questionnaire of hoarding severity; total score range = 0 to 92; higher values indicate more symptoms
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change from baseline to week 12; change from baseline to week 26
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hoarding Rating Scale
Time Frame: change from baseline to week 12; change from baseline to week 26
|
Interviewer measure with 5 questions to assess hoarding severity; total score range = 0 to 40; higher values indicate more symptoms
|
change from baseline to week 12; change from baseline to week 26
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Gail Steketee, Boston University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R21MH068539 (NIH)
- DATR A2-AIA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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