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The Effectiveness of Unified Protocol for Transdiagnostic Treatment on people with Separation Anxiety Disorder

The Effectiveness of Unified Protocol for Transdiagnostic Treatment on Symptoms and Emotional and Cognitive indices of Adults with Separation Anxiety Disorder Comorbid with Emotional Disorders: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240227061119N1
Enrollment
34
Registered
2024-07-23
Start date
2024-07-10
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Adult separation anxiety disorder.

Interventions

Sponsors

The University of Kurdestan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Having the diagnostic criteria DSM-5-TR for separation anxiety disorder and comorbid emotional disorders, and not taking drugs related to disorder. Consent to participate in the research Being at least 18 years old Having at least a diploma Not receiving any type of treatment related to the disorder during the past year Speak Persian fluently Ability to participate in all assessment and treatment sessions

Exclusion criteria

Exclusion criteria: Receiving any other type of psychological treatment Having any type of personality disorder and diagnosing any type of psychiatric disorder (except for emotional disorders) Substance abuse Having serious thoughts about Suicide Taking medications related to disorders

Design outcomes

Primary

MeasureTime frame
Separation anxiety score in adult separation anxiety questionnaire. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Adult Separation Anxiety Questionnaire (ASA-27).;Cognitive fusion score in cognitive fusion questionnaire. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Cognitive fusion Questionnaire (CFQ).;Anxiety sensitivity score in anxiety sensitivity questionnaire. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Anxiety Sensitivity Questionnaire (ASI).;Intolerance of uncertainty score in intolerance of uncertainty questionnaire. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Intolerance Uncertainty Questionnaire (IUS).;Emotion regulation score in the emotion regulation difficulty scale. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Difficulties Emotion Regulation scale (DERS).;Anxiety score in dass21 questionnaire. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Dass21 questionnaire.;Depression score in dass21 questionnaire. Timepoint: Pre-treatment; post-treatment; follow-up. Method of measurement: Dass21 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeideh Sobhani

The University of Kurdestan

saeideh.sobhani@uok.ac.ir+98 31 4261 7092

Outcome results

None listed

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