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Pilot Study of Vestibular Rehabilitation Training for Panic Disorder With Vestibular Dysfunction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00004366
Enrollment
20
Registered
1999-10-19
Start date
1995-08-31
Completion date
2000-05-31
Last updated
2005-06-24

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

Conditions

Agoraphobia, Panic Disorder, Vestibular Diseases

Keywords

agoraphobia, anxiety disorder, disease-related problem/condition, neurologic and psychiatric disorders, panic disorder, rare disease, vestibular diseases

Brief summary

OBJECTIVES: I. Evaluate whether vestibular rehabilitation training is of value in reducing anxiety symptoms in patients with panic disorder with or without agoraphobia who have vestibular dysfunction as identified by clinical vestibular tests.

Detailed description

PROTOCOL OUTLINE: During the first 4 weeks of study, patients meet with a clinical nurse specialist once a week for approximately 1 hour. During this time, the nature of the anxiety disorder is explained and exposure to previously feared situations is encouraged. Only patients who remain symptomatic at a stable level following self-exposure will proceed with rehabilitation training. Patients meet with a physical therapist once a week for 4 weeks to further evaluate the extent of problems associated with balance. Then, patients undergo weekly 1 hour exercises for 8 weeks with the physical therapist, focusing on sensation, head and eye coordination, movement with eyes opened and closed, and gait. Concurrently, patients meet with the clinical nurse specialist every 4 weeks during and after physical therapy to evaluate the effects of vestibular treatment on anxiety symptoms. Training is continued if patient is symptomatic; otherwise, patient is discharged from study.

Interventions

PROCEDUREPhysical therapy

Sponsors

University of Pittsburgh
CollaboratorOTHER
National Center for Research Resources (NCRR)
Lead SponsorNIH

Study design

Primary purpose
ECT

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed panic disorder with or without agoraphobia * Vestibular dysfunction, as defined by abnormalities in the caloric and/or rotational tests * Continued symptomatology after general instructions of the importance of exposure to feared situations * Absence of acute symptoms of anxiety or depression assessed to need immediate clinical care

Outcome results

None listed

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