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A Brief Version of Biofeedback Therapy for Panic Disorder

Not Applicable
Completed
Conditions
Feedback, Psychological
Panic Disorder
Interventions
Behavioral: Biofeedback therapy
Registration Number
NCT02826096
Lead Sponsor
National Taiwan University Hospital
Brief Summary

The study is to examine the therapeutic effect of a brief version of biofeedback therapy (developed bu the research team) on panic disorder. It is a randomized controlled design. The severity of panic symptoms of two groups of panic patients (reveiving biofeedback therapy or not) were measured before and after the six week duration. Besides, the severity of anxiety, depressive, somatic symptoms, and physiological indexes were recorded.

Detailed Description

The purpose of this study is trying to find out whether our newly developed brief version of biofeedback is an effective treatment approach for panic disorder. At the same time, the investigators want to clarify the change of bio- and psycho- indices present through the process. Patient recently experienced panic attacks are recruited in this study. The diagnosis of "Panic Disorder" is made by psychiatrists according to The Diagnostic and Statistical Manual of Mental Disorders(DSM-5) criteria. Subjects are randomly assigned to medication group or biofeedback therapy. The biofeedback therapy is conducted by psychologists following the structure way. Every subject will be measured both the bio and psycho indices on week 0, 3, and 6 under 6-week observation. In the end of the study, the investigators hope to analyze and clarify the treatment effects of our design, and also to exam the meanings of these indices, in order to find out an effective treatment approach.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
34
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
biofeedback groupBiofeedback therapybiofeedback therapy
Primary Outcome Measures
NameTimeMethod
Changes from baseline Panic Disorder Severity Scale (PDSS)week 0, week 3, week 6

PDSS is a scale rating the severity of panic disorder. It is a 5-point Likert scale with 7 items. The scores range from 0 (lowest level of panic disorder) to 28 (highest level of panic disorder).

Secondary Outcome Measures
NameTimeMethod
Scores of Health Anxiety Questionnaire (HAQ)week 0, week 3, week 6

HAQ is a scale rating the severity of health anxiety. It is a 4-point Likert scale with 21 items. The scores range from 0 (lowest level of health anxiety) to 63 (highest level of health anxiety).

Penn State Worry Questionnaire (PSWQ)week 0, week 3, week 6

PSWQ is a scale rating the severity of worry. It is 5-point Likert scale with 16 items. The scores range from 1 (lowest level of worry) to 80 (highest level of worry).

Scores of Beck Depression Inventory-II (BDI-II)week 0, week 3, week 6

BDI- II is a scale rating the severity of depression. It is a 4-point Likert scale with 21 items. The scores range from 0 (lowest level of depression) to 63 (highest level of depression).

Scores of Patient Health Questionnaire-15 (PHQ-15)week 0, week 3, week 6

PHQ-15 is a scale rating the severity of somatic distress. It is a 3-point Likert scale with 15 items. The scores range from 0 (lowest level of somatic distress) to 30 (highest level of somatic distress).

Sheehan Function Inventoryweek 0, week 3, week 6

It is a scale rating the function in various dimensions of work, social life, leisure activities, family life and family responsibilities.

Scores of WHOQOL-BREFweek 0, week 3, week 6

It is a self-report questionnaire measuring health-related quality of life. It is a 4-point Likert scale with 28 items, which belong to 5 domains (the overall, physical, psychological, social and environmental domains). The scores of each domain are usually normalized with 0-20 or 0-100.

Scores of Beck Anxiety Inventory (BAI)week 0, week 3, week 6

BAI is a scale rating the severity of anxiety. It is a 4-point Likert scale with 21 items. The scores range from 0 (lowest level of anxiety) to 63 (highest level of anxiety).

Degree of Change in Physiological Parametersweek 0, week 6

ProComp5 Infiniti (SA7525) Biofeedback System would be used. Heart rate variability, skin conductance, body temperature and respiratory rate would be measured.

Trial Locations

Locations (1)

National Taiwan University Hospital

🇨🇳

Douliu, Yun-Lin, Taiwan

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