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Agoraphobia clinical trials

View clinical trials related to Agoraphobia.

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NCT ID: NCT00202709 Completed - PTSD Clinical Trials

Can Thought Field Therapy (TFT) be Helpful for Patients With an Anxiety Disorder?

Start date: May 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if Thought Field Therapy has effect on certain anxiety disorders; agoraphobia, social phobia, and post traumatic stress disorder (PTSD).

NCT ID: NCT00004366 Completed - Panic Disorder Clinical Trials

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

Start date: August 1995
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT00000368 Completed - Panic Disorder Clinical Trials

Treatment of Panic Disorder: Long Term Strategies

Start date: February 1999
Phase: Phase 3
Study type: Interventional

Cognitive behavior therapy (CBT) with or without medication has been used in the treatment of panic disorder (PD). The purpose of this study is 1) to determine whether nine months of maintenance cognitive-behavior therapy (CBT) significantly improves the likelihood of sustained improvement; and 2) to determine the acute acceptability and efficacy of medication therapy or continued CBT alone among patients who fail to respond sufficiently to an initial course of CBT alone. It has been found that patients with PD respond as well to CBT or medication alone as they do to a combination of the two. Since the combined treatments are expensive and CBT is associated with less risk of medical toxicity compared to medications, CBT alone will be used first. All patients will first receive CBT alone. If the patient responds to this therapy, the patient will be assigned randomly (like tossing a coin) to 1 of 2 groups. One group will continue to receive CBT (maintenance therapy) for 9 months. The other group of responders will not receive any further therapy. If a patient does not respond to CBT alone, he/she will be assigned randomly to 1 of 2 different groups. One group will receive paroxetine; the other will continue to receive CBT for a longer period. The response to treatment will be evaluated to see which regimen works best to treat PD. The study will last approximately 3 years. An individual may be eligible for this study if he/she has panic disorder with no more than mild agoraphobia (fear of being in public places) and is at least 18 years old.