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Agoraphobia clinical trials

View clinical trials related to Agoraphobia.

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NCT ID: NCT02150265 Completed - Depression Clinical Trials

Effectiveness of Six Sessions CBT for Adolescents With Emotional Problems in Community Clinics

SMART
Start date: January 1, 2013
Phase: N/A
Study type: Interventional

Background: There is need for more effectiveness studies concerning treatment of emotional symptom problems indicating anxiety and depression in adolescents. SMART is the only treatment manual for combined emotional disorders developed in Norwegian. Purpose: To find the best individualized treatment for adolescents with emotional difficulties by: Finding criteria for the selection of appropriate patients for treatment with cognitive-behavior therapy program SMART in an outpatient population (14-18 years). Finding predictors of completion of treatment program SMART. Examining the effects of treatment with the SMART program at 6 months follow-up. Design: A randomized controlled study in six outpatient clinics in the north of Norway. N= 160 referred adolescents (14-18 years) with score above 6 on the Emotional Problems scale of the Strength and Difficulties Questionnaire (SDQ). Two thirds are treated according to the SMART-manual immediately, while the waiting list control group is treated with SMART after six weeks. Hypothesis: The SMART treatment is an effective treatment for emotional symptom problems. Publication: The results sought published internationally and nationally and will be communicated to clinicians.

NCT ID: NCT01928823 Completed - Agoraphobia Clinical Trials

Augmentation of Psychotherapy With D-Cycloserine in Agoraphobia

Exposure-DCS
Start date: November 2011
Phase: Phase 2
Study type: Interventional

Since decades, D-Cycloserine (DCS, drug class: Oxazolidinone) is proven to be an effective antibiotic agent in the treatment of tuberculosis. Furthermore it takes action in the central nervous system as an partial agonist on NMDA receptors. Because of glutamate mediated neuronal long-term potentiation in long-term memory DCS has an augmenting effect on emotional learning, as it occurs in exposure therapy of anxiety disorders. In this context we use DCS in addition to exposure therapy as a part of cognitive behavioral therapy (CBT) in patients suffering from agoraphobia with or without panic disorder. Thereby DCS is applicated oral as a capsule of 50mg, on three consecutive therapy sessions.

NCT ID: NCT01928810 Completed - Panic Disorder Clinical Trials

Physical Activity and Cognitive Behavioural Therapy in Panic Disorder and Agoraphobia

Start date: March 2011
Phase: N/A
Study type: Interventional

Physical activity (treadmill) prior to in-vivo exposure supports the effect of cognitive behavioural therapy in patients with panic disorder and agoraphobia.

NCT ID: NCT01680237 Terminated - Clinical trials for Panic Disorder With Agoraphobia

Cognitive Behavior Therapy vs Exposure in Vivo in the Treatment of Panic Disorder With Agoraphobia

Start date: October 2011
Phase: N/A
Study type: Interventional

Panic disorder with agoraphobia is a prevalent and one of the most handicapping anxiety disorders. Although the efficacy of psychological treatment for panic disorder with agoraphobia has been the subject of a great deal of research, studies comparing cognitive-behavioral therapy and exposure in vivo have regularly been underpowered to detect small to moderate differences. Therefore, the primary purpose of the present study is to investigate if the combination of cognitive techniques with exposure in vivo is superior to the effects of exposure alone for patients with moderate to severe agoraphobia.

NCT ID: NCT01606592 Completed - Clinical trials for Panic Disorder (With or Without Agoraphobia)

Psychotherapy Outcome and Self-selection Effects in Panic Disorder

Start date: January 2010
Phase: N/A
Study type: Interventional

The efficacy of two forms of psychotherapy with panic disordered patients, a cognitive-behavioral and a psychodynamic one, are compared under two different, randomized conditions: randomization or self-selection. The basic hypotheses are that the efficacy of both treatments is higher and that the efficacy difference is smaller under self-selection than randomized conditions.

NCT ID: NCT01446172 Completed - Agoraphobia Clinical Trials

Longterm Outcome of Inpatient Cognitive and Behavioral Therapies for Agoraphobia

Start date: November 2009
Phase: N/A
Study type: Observational

While cognitive therapy and exposure therapy are both proven to be effective for panic disorder and/or agoraphobia when outcome is assenssed up to one year after treatment (Gould et al., 1995) the scientific knowledge about long-term course of these disorders is still scanty. Although several long-term outcome studies have been conducted, the quality of these studies has been questioned. The aim is to conduct a follow-up study of patients with either panic disorder with history of agoraphobia or agoraphobia without history of panic disorder. the patients were treated in a group format at Modum Bad during the years 1989 to 1997. Four subsamples will be included in the study. Subsample 1 (76 patients treated in 1989 and 1990) received combined cognitive and psychodynamic treatment. Subsample 2 and 3 (46 patients treated in 1992 - 1993) were allocated to either cognitive therapy or guided mastery treatment. Subsample 4 (45 patients treated in 1994 - 1996) received cognitive and schema focused therapy. In the follow-up study the participants will be requested to complete the same self report measures as they completed at intake, discharge and at previous follow-up times. the participants will also be interviewed using the SCID-I and II as they were at the previous assessments. The present sample is relatively unique in having received pure psychosocial experimental treatments. The very long term efficacy of cognitive therapy relative to behavioural treatmetns for agoraphobia can be evaluated, and the potential moderating effects of personality disorders can be assessed.

NCT ID: NCT01323556 Recruiting - Panic Disorder Clinical Trials

Mechanisms of Panic Disorders Treatment

Start date: March 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Investigation of mechanisms of exposure based learning by 1. Investigating the effects of fear augmentation by interoceptive exposure during in vivo exposure 2. Disentangling the effects of interoceptive exposure exercises in panic disorder

NCT ID: NCT01025908 Completed - Panic Disorder Clinical Trials

Cognitive Behavior Psychotherapy in Panic Disorder

Start date: May 2006
Phase: N/A
Study type: Interventional

The objective of this study in cognitive-behavioural therapy (CBT) was to demonstrate the preparation of the patient with panic disorder for agoraphobic exposures. The focus of the work consisted of interoceptive exposures, in vivo, of body sensations themselves, to feared places and situations. The sample consisted of 50 individuals. Group 1 undertook 10 weekly, individual sessions of CBT of one hour duration. Group 2, control, was just follow-up with supportive therapy. The procedures used for the exposures, especially for induction symptom exercises, were considered essential in the preparation of patients with panic disorder, to be able to face up to panic attacks and subsequent agoraphobic situations.

NCT ID: NCT00932919 Completed - Agoraphobia Clinical Trials

Thought Field Therapy and Cognitive Therapy for Agoraphobia

Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose for this study is to find out if Thought field therapy has the same effect as, or better effect than, Cognitive therapy for Agoraphobia.

NCT ID: NCT00734370 Completed - Panic Disorder Clinical Trials

Virtual Reality Exposure Therapy in Agoraphobic Participants

Start date: October 2008
Phase: N/A
Study type: Interventional

Virtual Reality Exposure Therapy (VRET) is an effective treatment for anxiety disorders, particularly for specific phobias as fear of heights and fear of flying (e.g. Powers & Emmelkamp, 2008). Recent technological advances (e.g. more realistic avatars) make research into the efficacy of VRET for participants with elevated agoraphobic symptoms desirable. Therefore, the aim of the present research proposal is to investigate the comparative efficacy of: 1. enhanced VRET making use of the latest avatar technology with 2. exposure in vivo in agoraphobic participants 3. wait-list control.