The comparing the efficacy of Specific Cognitive Behavioral Protocol and Unified Protocol in reducing anxiety sensitivity, anxiety, depression and negative affect

Not Applicable

• Conditions: Panic disorder [episodic paroxysmal anxiety] without agoraphobia; Major depressive disorder, recurrent, mild; Symptoms and signs involving emotional state; Condition 1: Panic disorder. Condition 2: Major depressive disorder. Condition 3: Emotional problems.

• Registration Number: IRCT20180501039497N1
• Lead Sponsor: Zanjan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 16 July 2018

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 36

Inclusion Criteria

Being a student
Residence in the Zanjan city
Tending to participate in research

Exclusion Criteria

Drug abuse
Personality disorders
Cardiovascular diseases
More than two sessions of absenteeism during the intervention
Not attending in any of the evaluation sessions

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Anxiety sensitivity. Timepoint: Pre-test, Post-test and follow up (two month after post-test). Method of measurement: Anxiety Sensitivity Index- 3 (ASI-III).

Secondary Outcome Measures

Name	Time	Method
Anxiety. Timepoint: Pre-test, Post-test and Follow up (Two month after post- test). Method of measurement: Beck Anxiety Inventory (BAI).;Depression. Timepoint: Pre-test, Post-test and Follow up (Two month after post-test). Method of measurement: Beck Depression Inventory-II (BDI-II).;Negative afect. Timepoint: Pre-test, Post-test and Follow up (Two month after post- test). Method of measurement: Positive and Negative Affect Schedule-Negative (PANAS-NA).