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Clinical Trials/KCT0008289
KCT0008289
Not yet recruiting
未知

The clinical effect of virtual reality- and inhibitory learning-based dynamic exposure therapy for panic disorder and agoraphobia

Hallym University Medical Center- Chuncheon0 sites90 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Hallym University Medical Center- Chuncheon
Enrollment
90
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Hallym University Medical Center- Chuncheon

Eligibility Criteria

Inclusion Criteria

  • a) Aged 18 to 64
  • b) Patients: Diagnosed with Panic Disorder (E) or Agoraphobia (F) by the Mini\-International Neuropsychiatric Interview (MINI). / Healthy: No current psychiatric disorders including panic disorder and agoraphobia
  • c) Enough verbal and cognitive abilities to understand the consent form, answer the questionnaire, and operate VR devices/programs
  • d) Received detailed explanation regarding the study, adequately understood them, and volunteerly decided and give consent to participate in the study

Exclusion Criteria

  • a) Patient: Moderate or more suicide tendency (C), current manic (not hypomanic) episode (D), current/lifetime psychotic disorders (L), or psychopathy (P) is diagnosed in the MINI. Or past diagnosis records of psychotic disorders or severe bipolar disorder. / Healthy: Current significant psychiatric disorders
  • b) Suicide attempts within recent six months
  • c) Current/past epilepsy or photosensitive syndrome
  • d) Visual impairment (except for correctable ametropia or dyschromatopsia)
  • e) auditory disorders or moderate or severe hearing loss
  • f) Impairment of voluntary movements that may hinder the operation of VR programs
  • g) Serious clinical problems in the cardiovascular system, digestive system, respiratory system, endocrine system, or central nervous system that make it difficult to participate in the study
  • H) Pregnant or lactating women
  • I) Those who are judged unsuitable for research due to other reasons by principal investigators or those in charge

Outcomes

Primary Outcomes

Not specified

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