Cognitive-Behavioral Treatment of Gambling
CBT/CM
Enhanced Cognitive Behavior Therapy for the Treatment of Pathological Gambling
1 other identifier
interventional
120
1 country
1
Brief Summary
This study will determine the effectiveness of cognitive behavior therapy (CBT) and contingency management (CM) in reducing gambling behaviors and other related problems in pathological gambling. Study hypothesis: Participants who receive CBT and CM will attend more treatment sessions and show better outcomes than those who receive CBT alone.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1
Started Nov 2002
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2002
CompletedFirst Submitted
Initial submission to the registry
July 6, 2005
CompletedFirst Posted
Study publicly available on registry
July 11, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2005
CompletedJuly 1, 2013
June 1, 2013
2.9 years
July 6, 2005
June 28, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (7)
Addiction Severity Index (ASI) gambling severity scores
amount spent gambling per gambling episode
longest period of non-gambling
days until first gambling episode
percent of days gambling
proportion meeting diagnostic criteria
number of treatment sessions attended
Secondary Outcomes (1)
Psychosocial functioning
Interventions
Receive 8 50-minute sessions of one-on-one cognitive behavioral therapy
Receive vouchers that can be spent on rewards for completing activities that support abstinence from gambling
Eligibility Criteria
You may qualify if:
- Diagnosis of pathological gambling
- At least 1 gambling episode within 30 days prior to study entry
- Able to read English at a 5th grade level
- Willing and able to comply with all study requirements
You may not qualify if:
- Uncontrolled psychiatric conditions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- UConn Healthlead
- National Institute of Mental Health (NIMH)collaborator
Study Sites (1)
University of Connecticut Health Center
Farmington, Connecticut, 06030, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nancy M. Petry, PhD
UConn Health
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
July 6, 2005
First Posted
July 11, 2005
Study Start
November 1, 2002
Primary Completion
October 1, 2005
Study Completion
October 1, 2005
Last Updated
July 1, 2013
Record last verified: 2013-06