Welcome
Support Centre
17 May 2012 
ISRCTN Register - International Standard Randomized Controlled Trial Number
Trial registration
Unique identification scheme
International databases
home  |   my details  |   ISRCTN Register  |   mRCT  |   links  |   information  |   press
Find trials
ISRCTN Register
tips on searching

Registration
New application
Updating record

Information
introduction
governing board
ISRCTN FAQs
data set
letter of agreement
request information
guidance notes

[ Print-friendly version ]
A randomised controlled trial of brief cognitive therapy for social phobia (social anxiety disorder)
ISRCTN ISRCTN11178360
ClinicalTrials.gov identifier
Public title A randomised controlled trial of brief cognitive therapy for social phobia (social anxiety disorder)
Scientific title
Acronym N/A
Serial number at source 069777
Study hypothesis To determine whether a new and brief (seven session), self-study augmented version of cognitive therapy for social phobia is as effective as the established, full length (14 session) treatment programme.
Lay summary
Ethics approval The research project has been reviewed and supported the Research Ethics Committee of the Department of Institute of Psychiatry and South London and Maudsley NHS Trust (ref: 05/Q0706/237).
Study design Randomised controlled trial
Countries of recruitment United Kingdom
Disease/condition/study domain Social Phobia
Participants - inclusion criteria To be included in the trial, patients must meet the following criteria:
1. Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) (American Psychiatric Association, 1994) criteria for social phobia
2. Duration of at least six months
3. Social phobia considered to be the patient's main problem
4. Age 18 to 65 years
5. No psychotropic medication or on a stable dose for at least two months without symptomatic improvement and willing to keep dosage constant during the trial
6. Agree not to start any additional non-protocol treatment during the trial
7. Willing to accept random allocation
Participants - exclusion criteria Patients who meet the inclusion criteria will be excluded if they also met the following criteria:
1. Current alcohol or substance dependency (abuse but not dependency is acceptable)
2. Current or past psychosis
3. Borderline personality disorder (other personality disorders are not a reason for exclusion)
4. Unable to read English
5. Social phobia previously treated with an adequate course of an appropriate course of cognitive behaviour therapy or exposure therapy
Anticipated start date 14/02/2006
Anticipated end date 01/02/2009
Status of trial Completed
Patient information material
Target number of participants 90 - recruitment ends on the 01/02/2008
Interventions Patients suffering from social phobia who are referred to the Centre for Anxiety Disorders and Trauma at the Maudsley Hospital will be invited to participate in the trial. Patients who agree to be included will initially be randomly allocated to:
1. Brief (seven sessions), self-study augmented cognitive therapy
2. Full cognitive therapy (14 sessions)
3. A 14 week wait-list control condition

Patients initially allocated to wait will subsequently receive brief or full cognitive therapy (further random allocation). Full cognitive therapy will be identical to the full cognitive therapy programme used in our recent randomised controlled trials. The self-study modules cover all the main steps in therapy and are completed in the days before a treatment session. The modules were developed and refined over a 12 month period in consultation with patients from the Centre for Anxiety Disorders and Trauma.

The aim of the modules is to speed up therapy by allowing therapists to focus more closely on areas that need a therapist's skill. As social phobia is a chronic condition, it is important that treatments have a sustained effect. For this reason, the proposed research trial includes a one year prospective follow-up after the end of treatment. In our previous trials of cognitive therapy, we have found that therapy gains are largely maintained at one year follow-up and we expect the same to be true in this trial. Other assessments will be at pre-treatment, mid-treatment, post-treatment and three month follow-up.
Primary outcome measure(s) The primary outcome measure for the trial is a social phobia composite measure that is created by combining scores from seven independent assessor and patient scales that are well validated measures of social phobia related symptomatology. Scores on each scale are standardised (M = 0, SD = 1) across pre-treatment and post-treatment assessments by converting to Z scores. The composite at each assessment occasion is the mean of the Z scores on that occasion. This procedure has been used in our last two social phobia trials as well as in other trials in the field.

The seven scales that make up the social phobia composite are:
1. The mean assessor rating of social phobia related fear and avoidance from the anxiety disorders interview schedule for DSM-IV
2. Patient completed Social Phobia Scale
3. The Social Interaction Anxiety Scale
4. The Liebowitz Social Anxiety Scale
5. The Social Phobia and Anxiety Inventory
6. The Fear of Negative Evaluation Scale
7. The Social Phobia Weekly Summary Scale
Secondary outcome measure(s) 1. General mood (assessed by the Beck Anxiety Inventory and the Beck Depression Inventory) and Disability (assessed by the Sheehan Disability Scales)
2. The proportion of patients who continue to meet diagnostic criteria for social phobia at post-treatment and follow-up and the proportion of patients who continue to meet diagnostic criteria for avoidant personality disorder at 12 month follow-up
Sources of funding The Wellcome Trust (UK) (grant ref: 069777)
Trial website
Publications
Contact name Prof  David M  Clark
  Address Institute of Psychiatry
Henry Wellcome Building
Department of Psychology
De Crespigny Park
  City/town London
  Zip/Postcode SE5 8AF
  Country United Kingdom
  Tel +44 (0)20 7848 0245
  Fax +44 (0)20 7848 0786
  Email d.clark@iop.kcl.ac.uk
Sponsor King's College London and the South London and Maudsley NHS Trust (UK)
  Address Dr Gill Dale, R&D Office
Institute of Psychiatry
De Crespigny Park
  City/town London
  Zip/Postcode SE5 8AF
  Country United Kingdom
  Tel +44 (0)20 7848 0675
  Fax +44 (0)20 7848 0147
  Email g.dale@iop.kcl.ac.uk
  Sponsor website: http://www.iop.kcl.ac.uk
Date applied 30/03/2006
Last edited 04/09/2007
Date ISRCTN assigned 30/03/2006
Submit your trial protocol
Submit to Trials journal
Follow us on Twitter
© 2012 ISRCTN unless otherwise stated.


BioMed Central