Pilot Trial of Cognitive and Behavioral Treatment of Compulsive Hoarding Compared to Wait List Control

Sponsor
Boston University Charles River Campus (Other)
Overall Status
Completed
CT.gov ID
NCT00073346
Collaborator
National Institute of Mental Health (NIMH) (NIH)
52
2
2
58.3
26
0.4

Study Details

Study Description

Brief Summary

This study developed and tested a specialized cognitive and behavioral treatment for the symptoms of hoarding disorder, including excessive acquiring, difficulty discarding items, and extensive clutter in the home.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Behavioral Treatment
Phase 1

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 Design

Study Type:
Interventional
Actual Enrollment :
52 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
active treatment versus wait list controlactive treatment versus wait list control
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Cognitive and Behavioral Treatment of Compulsive Hoarding
Actual Study Start Date :
Sep 1, 2003
Actual Primary Completion Date :
Dec 1, 2006
Actual Study Completion Date :
Jul 9, 2008

Arms and Interventions

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.

Behavioral: Cognitive Behavioral Treatment

No Intervention: Wait list control

Participants waited to receive treatment for 12 weeks

Outcome Measures

Primary Outcome Measures

  1. Saving Inventory-Revised [change from baseline to week 12; change from baseline to week 26]

    Self-report questionnaire of hoarding severity; total score range = 0 to 92; higher values indicate more symptoms

Secondary Outcome Measures

  1. Hoarding Rating Scale [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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hartford Hospital, Institute of Living Hartford Connecticut United States 06106
2 BostonUCRC Boston Massachusetts United States 02215

Sponsors and Collaborators

  • Boston University Charles River Campus
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Gail Steketee, Boston University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Boston University Charles River Campus
ClinicalTrials.gov Identifier:
NCT00073346
Other Study ID Numbers:
  • R21MH068539
  • R21MH068539
  • DATR A2-AIA
First Posted:
Nov 21, 2003
Last Update Posted:
Jan 21, 2020
Last Verified:
Jan 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Boston University Charles River Campus
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 21, 2020