Feasibility Study of Unified Protocol for Anxiety and Depressive Disorders

INTERVENTION: CBT (Unified Protocol) CONDITION: Anxiety Disorders, Depressive Disorders PRIMARY OUTCOME: Severity of anxiety symptoms assessed by the SIGH‐A (0 week vs 1 week after the completion of intervention) SECONDARY OUTCOME: 1. Diagnoses assessed by the M.I.N.I.; 2. Objective severity of depressive symptoms (GRID‐HAM‐D); 3. Subjective severity of depressive symptoms (BDI‐II); 4. Quality of Life (EuroQol etc); 5. Subjective symptoms for primary diagnosis (self‐report scale); 6. Emotion Regulation (ERQ); 7. Experienced Emotion (PANAS); 8. Drop Out rates; 9. Adverse Events INCLUSION CRITERIA: 1. Subjects with current DSM‐IV Panic disorder with/without Agoraphobia, Agoraphobia without history of Panic Disorder, Specific Phobia, Social Phobia (Social Anxiety Disorder), Obsessive‐Compulsive Disorder, Post‐Traumatic Stress Disorder, Generalized Anxiety Disorder, Anxiety Disorder Not Otherwise Specified, Major Depressive Disorder, Depressive Disorder Not Otherwise Specified 2. HAM‐D Anxiety Factor >= 7 3. Age 20 years or older, and 65 years or younger at screening. 4. Subjects who give full consent in the participation of the study