Cognitive Behaviour Therapy: Treatment Administered Via Videoconference Versus In-Perso
Not Applicable
Recruiting
- Conditions
- In accordance with the Diagnositic Statistical Manual of mental disorder-4th edition, participants will have to meet the criteria for a diagnosis on the depression and anxiety spectrum, which includes but not limited todepression, dysthymia, generalized anxiety disorder, panic disorder with and without agoraphobia, social phobia, specific phobia, obsessive-compulsive disorder and post-traumatic stress disorder.Mental Health - DepressionMental Health - Anxiety
- Registration Number
- ACTRN12609000819224
- Lead Sponsor
- Curtin University of Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 115
Inclusion Criteria
Diagnostic Statistical Manual for mental disorder (4th Edition): diagnosis on the depression and anxiety spectrum, which includes but not limited to; depression, dysthymia, generalized anxiety disorder, panic disorder with and without agoraphobia, social phobia, specific phobia, OCD and PTSD.
Exclusion Criteria
Anorexia, Personality disorder as the primary diagnosis, Self-harming/suicidal, Involved in legal proceedings, Psychosis (past or present)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the efficacy of cognitive behavioural psychotherapy via videoconference. <br><br>Structured Interview For the DSM-IV- will be used for assessmetn and diagnosis. <br>Primary Measures:<br>Depression Anxiety Stress scale (DASS)<br>Quality Of Life & Satisfaction Questionnaire (Q-LES)<br>This will assessed by using a 2x3 (VC-F2F x pre-post-follow up) Analysis of Covariance.[November 2009- January 2011<br><br>All participants will be treated within this period. When their assessment/diagnosis occurs depend on when they are referred to the Curtin Psychology Clinic. The questionnaires used on the day of the first assessment will constitute the pre-treatment measure. Treatment will be conducted for a maximum of 12 weeks. Measures administered at the start of treatment will also be provided at the end of treatment (post-treatment data). Then 6-weeks after treatment has ended the same questionnaires will be given to participants, which will constitute the follow-up data.]
- Secondary Outcome Measures
Name Time Method