Anxiety Disorders Clinical Trial
Official title:
Randomized Controlled Trial Examining the Effectiveness of Two Group Psychotherapies for Anxiety Disorders: Unified Cognitive-behavioral Therapy vs. Combined Cognitive Behavioral and Dance/Movement Therapy
Verified date | April 2016 |
Source | Shalvata Mental Health Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | Israel: Ethics Commission |
Study type | Interventional |
The current pilot study will examine and compare the effectiveness of two group
psychotherapies for mixed anxiety disorders: 1. unified cognitive-behavioral protocol,
adapted to a group format. 2. combined cognitive-behavioral and dance/movement therapy.
In addition, change in proposed mechanism in each therapy will be examined, along with their
association with change in outcome measures during therapy.
Status | Active, not recruiting |
Enrollment | 24 |
Est. completion date | September 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 20 Years to 65 Years |
Eligibility |
Inclusion Criteria: - One of the following primary axis I DSM-IV-TR diagnoses: Panic disorder with or without Agoraphobia; Social Anxiety Disorder; Generalized Anxiety Disorder; Anxiety Disorder Not Otherwise Specified; Adjustment Disorder With Anxiety; Adjustment Disorder With Mixed Anxiety and Depressed Mood - If on medication or in other types of treatments, patients must be willing to remain stable on their treatment for the duration of the acute phase of the study (5-6 months) - Provision of written informed consent Exclusion Criteria: - Current or past schizophrenia, psychosis, or bipolar disorder. - Current suicidal ideation. - Current substance/alcohol dependence or abuse. - Cluster A or B personality disorder. - Pregnancy (for women). |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | Shalvata Mental Health Center | Hod Hasharon |
Lead Sponsor | Collaborator |
---|---|
Shalvata Mental Health Center |
Israel,
Barlow DH, Farchione TJ, Fairholme CP, Ellard KK, Boisseau CL, Allen LB, Ehrenreich-May J. The Unified Protocol for Transdiagnostic Treatment of Emotional Disorders: Therapist Guide. New York: Oxford University Press: 2011.
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in Difficulties in Emotion Regulation Scale | Self-report measure of different aspects of emotion regulation difficulties | Intake (entry to study), Weekly during treatment (weekly between 1-6 months from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Other | Change in Body Sensations Questionnaire | Self-report measure of fear of bodily sensations | Intake (entry to study), Pre-treatment (1 month from intake), Mid-Treatment (3.5 months from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Other | Change in Bodily Awareness of Emotions Subscale of the Emotion Awareness Questionnaire - Revised | Self-report measure of awareness of bodily sensations/movement and their emotional meaning | Intake (entry to study), Pre-treatment (1 month from intake), Mid-Treatment (3.5 months from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Other | Change in Working Alliance Inventory - Short and Revised form - Group version | Self-report measure of working alliance in group therapy | Intake (entry to study), Pre-treatment (1 month from intake), Session 5 (2 months from intake), Mid-Treatment (3.5 months from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Primary | Change in Hamilton Anxiety Rating Scale | Structured independent evaluator interview for assessing severity of anxiety | Intake (entry to study), Pre-treatment (1 month from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Secondary | Change in Depression, Anxiety, Stress Scales-21 | Self-report measure of depression, anxiety and stress | Intake (entry to study), Weekly during treatment (weekly between 1-6 months from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Secondary | Change in Valued Living Questionnaire | Self-report measure of valued living | Intake (entry to study), Pre-treatment (1 month from intake), Mid-Treatment (3.5 months from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
Secondary | Change in Mini International Neuropsychiatric Interview | Structured independent evaluator interview for assessing Diagnostic and Statistical Manual of Mental Disorders IV Text Revision (DSM-IV-TR) axis I diagnoses | Intake (entry to study), Pre-treatment (1 month from intake), Post-Treatment (6 months from intake), Follow-Up (7 months from intake) | No |
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