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A Validation Study of Mobile Virtual Reality-Based Self-Care and Exposure Therapy Contents for the Treatment of Panic Disorder

Y

Yonsei University Health System (YUHS)

Status

Completed

Conditions

Panic Disorder

Treatments

Procedure: Arm I (Prepectoral)
Other: Arm II (Subpectoral)

Study type

Interventional

Funder types

Other

Identifiers

NCT04985019
3-2018-0292

Details and patient eligibility

About

The purpose of this study is to determine whether mobile-based virtual reality exposure treatement can reduce the symptoms of panic disorder and the symptoms of depression and anxiety than the waitlist group

Enrollment

40 patients

Sex

All

Ages

19 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meet Diagnostic Statistical Manual criteria for panic disorder(with or without agoraphobia) .

No change in drug dosage during the study period

Exclusion criteria

  • Patients with a history of major neurological or significant medical illness, or met the diagnostic criteria of current substance misuse

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

I (Prepectoral)
Experimental group
Description:
VR treatment group Participants received the Self-Guided Virtual Reality-based Cognitive Behavioral Therapy for panic disorder.
Treatment:
Procedure: Arm I (Prepectoral)
Other: Arm II (Subpectoral)
II (Subpectoral)
No Intervention group
Description:
Waiting list Participants in a waiting list.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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