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Treatment of Panic Disorder Via Internet With a Wireless Temperature Biofeedback Ring

A Study on Mental Health Care by Using Specific Vital Signs

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00825136
Enrollment
10
Registered
2009-01-19
Start date
2008-07-31
Completion date
2009-05-31
Last updated
2012-08-21

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

Conditions

Panic Disorder

Keywords

Panic Disorder, Temperature Biofeedback, Internet

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.

Interventions

BEHAVIORALrelaxation

Participants were asked to log in the system to keep the muscle relaxation program every day and complete some self-rating scales on browser every week.

BEHAVIORALbiofeedback (finger temperature biofeedback)

Participants were asked to log in the system to keep the muscle relaxation program plus finger temperature biofeedback every day and complete some self-rating scales on browser every week.

Sponsors

Chimei Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. The participant must fulfill DSM-IV criteria for panic disorder. 2. The participant must be between 18 and 60 years of age. 3. The participant must have panic disorder as the primary problem. 4. 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. 5. If the participant was already in therapy, the contact must have lasted at least 6 months and not be based on cognitive behavior therapy. 6. All participants have access to a computer with an Internet connection.

Exclusion criteria

1. The participant suffers from any other psychiatric disorder in immediate need of treatment. 2. The participant fulfills DSM-IV criteria for major depression. 3. The participant has epilepsy, kidney problems, strokes, organic brain syndrome, emphysema, heart disorders, or chronic hypertension. 4. The participant has alcoholism.

Design outcomes

Primary

MeasureTime frame
score change of The Panic Disorder Severity Scale(PDSS)day 1 / 4 weeks/ 8 weeks

Secondary

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

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026