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

The comparing the efficacy of Specific Cognitive Behavioral Protocol and Unified Protocol in reducing student?s anxiety sensitivity, anxiety, depression and negative affect: Double Blind Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180501039497N1
Enrollment
36
Registered
2018-06-10
Start date
2018-09-23
Completion date
Unknown
Last updated
2018-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Interventions

Intervention 1: First intervention group: Cognitive behavioral Therapy by Margo and Stewart's Protocol. Intervention 2: Second intervention group: Transdiagnostic of emotional disorders by Unified Pro

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Saed

Zanjan University of Medical Sciences

o.saed@zums.ac.ir+98 24 3354 2403

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026