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Clinical Trials/NCT00825136
NCT00825136
Terminated
N/A

A Study on Mental Health Care by Using Specific Vital Signs

Chimei Medical Center1 site in 1 country10 target enrollmentJuly 2008
ConditionsPanic Disorder

Overview

Phase
N/A
Intervention
Not specified
Conditions
Panic Disorder
Sponsor
Chimei Medical Center
Enrollment
10
Locations
1
Primary Endpoint
score change of The Panic Disorder Severity Scale(PDSS)
Status
Terminated
Last Updated
13 years ago

Overview

Brief Summary

Internet plays a more and more important role in many applications of healthcare. Many researches on the integrations of internet and mental health care have been proposed in recent years. This project aims at the development of an online treatment system which combines the biofeedback therapy and the web technologies to treat the patients suffering from panic disorder with partial response to medications. This project also evaluates the efficacy of a new- designed wireless temperature biofeedback ring.

Detailed Description

The participants should be chronic panic patients. They login an web-based server and practice muscle relaxation on-line every day. There will be two two parallel groups: one group practicing muscle relaxation only and the other practicing muscle relaxation with finger surface temperature monitor through a wireless biofeedback ring.

Registry
clinicaltrials.gov
Start Date
July 2008
End Date
May 2009
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Chimei Medical Center
Responsible Party
Principal Investigator
Principal Investigator

Fong-Lin Jang

Department of Psychiatry

Chimei Medical Center

Eligibility Criteria

Inclusion Criteria

  • The participant must fulfill DSM-IV criteria for panic disorder.
  • The participant must be between 18 and 60 years of age.
  • The participant must have panic disorder as the primary problem.
  • If the participant is taking prescribed drugs for panic disorder, a) the dosage have to be constant for 2 months before starting treatment, and b) the participant have to agree to keep the dosage constant for 1 month after starting treatment.
  • If the participant was already in therapy, the contact must have lasted at least 6 months and not be based on cognitive behavior therapy.
  • All participants have access to a computer with an Internet connection.

Exclusion Criteria

  • The participant suffers from any other psychiatric disorder in immediate need of treatment.
  • The participant fulfills DSM-IV criteria for major depression.
  • The participant has epilepsy, kidney problems, strokes, organic brain syndrome, emphysema, heart disorders, or chronic hypertension.
  • The participant has alcoholism.

Outcomes

Primary Outcomes

score change of The Panic Disorder Severity Scale(PDSS)

Time Frame: day 1 / 4 weeks/ 8 weeks

Secondary Outcomes

  • score change of MOS 36-Item Short-Form Health Survey (SF-36)(day 1 / 4 weeks/ 8 weeks)

Study Sites (1)

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