Skip to content

The Study of the Use of Physiological Markers in Digital Cognitive Behavioral Therapy for Panic Disorder

The Study of the Use of Physiological Markers in Digital Cognitive Behavioral Therapy for Panic Disorder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010050
Enrollment
84
Registered
2024-12-16
Start date
2023-11-13
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None listed

Interventions

Others : Panic Disorder-Experimental Group (n=28): Participants will be provided with a digital Cognitive Behavioral Therapy (dCBT) application focused on Interoceptive Exposure Therapy. All participa

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: To be eligible for the study, individuals must meet all of the following criteria: 1) Are diagnosed with panic disorder or a panic attack specifier by a psychiatrist according to DSM-5 criteria. 2) Score 7 or above on the Korean version of the Panic Disorder Severity Scale. 3) Are able to understand and participate in cognitive behavioral therapy. 4) Are able to use wearable devices and the application. 5) Have listened to the explanation of this study and have consented to participate.

Exclusion criteria

Exclusion criteria: Individuals will be excluded from the study if they meet any of the following criteria: 1) Are participating in another therapy program that prohibits concurrent participation in non-pharmacological treatment programs, or have received cognitive behavioral therapy for panic disorder within the past three months. 2) Have accompanying internal medicine or neurological disorders. 3) Exhibit current psychotic symptoms. 4) Are diagnosed with schizophrenia, schizoaffective disorder, cognitive disorders, or impulse control disorders. 5) Are assessed to have a high risk of suicide during a clinical interview.

Design outcomes

Primary

MeasureTime frame
Panic Disorder Severity Scale (PDSS)

Secondary

MeasureTime frame
Interoceptive fear/avoidance subfactor score of the PDSS;Albany Panic and Phobia Questionnaire (APPQ);Panic Disorder Severity Scale - Self rating (PDSS-SR);Anxiety Severity Index-Revised (ASI-R);Beck Anxiety Inventory (BAI);Beck Depression Inventory (BDI);Subjective Units of Disturbance scales (SUDs);Heart Rate;Heart Rate Variability;Skin conductance;Prothrombin Time (PT), activated partial thromboplastin time(aPTT), von Willebrand factor, Thrombin- AntiThrombin complex (TAT complex), Plasminogen activator inhibitor-1, plasminogen, fibrinogen, D-dimer, Coagulation Factor VII, contact activation system;Digital phenotype (Keytstroke dynamics, step , illuminance, GPS);Digital literacy;Usability evaluation of the app and wearable device;quantitative electroencephalograph (qEEG);Clinical Global Impression (CGI)

Countries

Korea, Republic of

Contacts

Public ContactSoo-Jin Kwak

Seoul National University Hospital

sujinkwak.lab@gmail.com+82-2-870-3464

Outcome results

None listed

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