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Clinical Trials/NCT00184106
NCT00184106
Completed
Phase 4

A Randomised, Triple Blind, Placebo-controlled Trial Comparing the Effects of Cognitive Therapy, Paroxetine and Both Cognitive Therapy and Paroxetine in the Treatment of Patients With Primary Social Phobia

Norwegian University of Science and Technology1 site in 1 country86 target enrollmentOctober 2004

Overview

Phase
Phase 4
Intervention
Seroxat, Cognitive therapy, Seroxat+ cognitive therapy
Conditions
Phobic Disorders
Sponsor
Norwegian University of Science and Technology
Enrollment
86
Locations
1
Primary Endpoint
The proportion responders as measured by FAIR OF NEGATIVE EVALUATION and SPAI at 12 and 24 week.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

We aim to (1) evaluate the effectiveness of cognitive therapy and paroxetine and their combination, (2) investigate the patterns of change and the mechanisms of action involved during treatment by using psycho-physiological assessments in order to delineate some of the cognitive, behavioural and physiological mechanisms in the patients' response to CT, to paroxetine and placebo.One hundred patients with a primary diagnosis of social phobia will be selected and randomised into four treatment conditions. The first group (N=25) will be treated with CT alone, the second group (N=25) with CT plus paroxetine, the third group (N=25) with paroxetine and clinical management (TAU), the fourth group will receive placebo and clinical management (N=25). All patients will have 12 weeks of treatment in the acute phase, which includes 12 sessions of individual treatment for the two first groups. The 2nd and 3rd groups will in addition have 12 weeks of drug treatment in the maintenance phase. The 4th group will have placebo for 24 weeks and clinical management. The patients will be assessed at pre-treatment, at 12 weeks and at the end of treatment of the acute phase (12 weeks) and by the end of maintenance phase (24 weeks). Follow-up will be at 6 and 12 months.

Measures are based on all three main sources; self-report inventories, clinical assessments by independent raters and psycho-physiological assessments.

Registry
clinicaltrials.gov
Start Date
October 2004
End Date
December 2010
Last Updated
7 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Signed written informed consent obtained prior to entry in the study.
  • Diagnosed with primary social phobia, generalized or specific (DSM-IV, APA, 1994).
  • Symptoms present at least one year.
  • Age between 18-65 years.

Exclusion Criteria

  • Known somatic diseases.
  • Pregnant (\*) or lactating women.
  • Acute suicidal symptoms
  • Major depressive disorder
  • Generalized Anxiety Disorder or PTSD
  • Cluster A or cluster B personality disorder
  • Substance abuse or dependence
  • Body dysmorphic disorder.
  • Not willing to accept random allocation.
  • Patients who take some form of SSRI medications currently or during the last 6 months

Arms & Interventions

Cognitive Therapy

Cognitive Therapy

Intervention: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy

Seroxat and SE

SSRI with Self exposure

Intervention: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy

Seroxat and Cognitive Therapy

Combination of Seroxat and Cognitive Therapy

Intervention: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy

Pill-Placebo

Pill Placebo

Intervention: Seroxat, Cognitive therapy, Seroxat+ cognitive therapy

Outcomes

Primary Outcomes

The proportion responders as measured by FAIR OF NEGATIVE EVALUATION and SPAI at 12 and 24 week.

Time Frame: December 2010

A patient is classified as responder if the decrease on FNE is equivalent with or above 40%.

Time Frame: December 2010

Secondary Outcomes

  • Relapse rate during 6 and 12 months of follow up.(December 2010)

Study Sites (1)

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