Residential Cognitive and Interpersonal Therapy for Social Phobia
Residential Cognitive Therapy Versus Residential Interpersonal Therapy for Social Phobia: A Randomized Controlled Trial
1 other identifier
interventional
80
1 country
1
Brief Summary
The purpose of this study is twofold: (1) to compare the effectiveness of two promising treatments for social phobia, a new cognitive therapy model (Clark \& Wells, 1995; Borge et al., 2001) and interpersonal therapy (Lipsitz, Markowitz, \& Cherry, 1997), adapted for inpatient groups; and (2) to study the empirical change processes in these therapies and compare them with the cognitive and interpersonal models of change.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_2
Started Oct 2001
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
October 1, 2001
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2004
CompletedFirst Submitted
Initial submission to the registry
May 15, 2006
CompletedFirst Posted
Study publicly available on registry
May 16, 2006
CompletedMay 16, 2006
May 1, 2006
May 15, 2006
May 15, 2006
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Social Avoidance
Social Anxiety
Secondary Outcomes (4)
General Anxiety
Depression
Interpersonal Problems
Personality Disorders
Interventions
Eligibility Criteria
You may qualify if:
- DSM-IV criteria for social phobia
- the patient consider social phobia as the main current problem
- willingness to suspend use of psychotropic medication, alcohol and other substances
- acceptance of random allocation
- ability to speak Norwegian
- age 18-65 years.
You may not qualify if:
- a history of recurrent major depression currently treated sucessfully with antidepressant medications
- has immediate need for additional treatment
- current psychotic disorder or substance abuse
- organic mental disorder
- previously treated with similar models
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Modum Badlead
Study Sites (1)
Modum Bad
Vikersund, Buskerud, N-3370, Norway
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Asle Hoffart, Dr Psychol
Modum Bad
- PRINCIPAL INVESTIGATOR
Finn-Magnus Borge, Cand Psychol
Modum Bad
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
May 15, 2006
First Posted
May 16, 2006
Study Start
October 1, 2001
Study Completion
June 1, 2004
Last Updated
May 16, 2006
Record last verified: 2006-05