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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT00912535 Completed - Clinical trials for Primary Anxiety Disorders

Quetiapine Augmentation for Primary Anxiety Disorder or Mood Disorders With Co-morbid Anxiety Symptoms

Start date: May 2009
Phase: Phase 4
Study type: Interventional

The objectives of this study are to evaluate the efficacy and safety of quetiapine extended release tablet versus placebo as adjunct to selective serotonin reuptake inhibitors/serotonin/norepinephrine reuptake inhibitors (SSRI/SNRI) in the augmentation treatment of patient with primary anxiety disorders or mood disorders with co-morbid anxiety symptoms.

NCT ID: NCT00903474 Completed - Breast Cancer Clinical Trials

Mindful Movement Program in Improving Quality of Life in Older Female Breast Cancer Survivors

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

RATIONALE: Mindful movement is a self-directed activity of mindfulness (intention, attention, and attitude) and physical movement. A mindful movement program may be effective in improving well-being in older women who are breast cancer survivors. PURPOSE: This randomized clinical trial is studying how well a mindful movement program works in improving quality of life in older female breast cancer survivors.

NCT ID: NCT00902564 Completed - Clinical trials for Generalized Anxiety Disorder

Escitalopram in Patients With Generalized Anxiety Disorder

Start date: March 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effect of escitalopram after 8 weeks of treatment in patients with Generalized Anxiety Disorder (GAD), to evaluate proportion of patients who respond to escitalopram during the treatment period, and to evaluate safety of escitalopram.

NCT ID: NCT00902330 Completed - Breast Cancer Clinical Trials

Cranial Stimulation for Chemotherapy Symptoms in Breast Cancer

Start date: April 2009
Phase: Phase 3
Study type: Interventional

RATIONALE: Cranial microcurrent electrical stimulation (CES) is mild electrical current received through electrodes placed on the earlobes. CES may lessen symptoms in women with breast cancer receiving chemotherapy. It is not yet known whether CES is more effective than sham therapy in reducing symptoms caused by chemotherapy in women with breast cancer. PURPOSE: This randomized phase III trial is studying mild electrical stimulation to see how well it works compared with sham therapy in reducing symptoms caused by chemotherapy in women with stage I, stage II, or stage IIIA breast cancer receiving chemotherapy.

NCT ID: NCT00902226 Completed - Clinical trials for Social Anxiety Disorder

Escitalopram in Patients With Social Anxiety Disorder

Start date: March 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effect of escitalopram after 12 weeks of treatment in patients with Social Anxiety Disorder (SAD), to evaluate proportion of patients who respond to escitalopram during the treatment period, and to evaluate safety of escitalopram.

NCT ID: NCT00887679 Completed - HIV Infections Clinical Trials

Treatment Effects of Escitalopram (Lexapro®) on Generalized Anxiety Disorder in Patients With HIV and AIDS

Start date: May 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether escitalopram is safe, well tolerated, and effective in the treatment of HIV-infected patients with generalized anxiety disorder.

NCT ID: NCT00879515 Completed - Anxiety Disorders Clinical Trials

Examining Social, Emotional, and Cognitive Functioning in People With Fragile X and Down Syndromes

Start date: October 2005
Phase: N/A
Study type: Observational

By testing physiological responses to anxiety in people with nervous system developmental disorders, this study will identify specific physiological characteristics associated with response to anxiety treatments.

NCT ID: NCT00872820 Completed - Clinical trials for Social Anxiety Disorder

Examining Long-Term Effects and Neural Mediators of Behavioral Treatments for Social Anxiety Disorder

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

This study will compare the effects that two types of behavioral therapy have on brain function in people with social anxiety disorder.

NCT ID: NCT00872131 Completed - Anxiety Disorders Clinical Trials

Identifying Brain and Genetic Markers of Sertraline Treatment Response in People With Social Anxiety Disorder

Start date: March 2008
Phase: Phase 4
Study type: Observational

This study will attempt to identify gene and brain activity markers that predict whether people with social anxiety disorder will respond to selective serotonin reuptake inhibitor medications.

NCT ID: NCT00865306 Completed - Anxiety Disorder Clinical Trials

Early Intervention for Children at Risk for Anxiety

Start date: March 1998
Phase: N/A
Study type: Interventional

The aim of this study was to develop and pilot a cognitive-behavioral therapy (CBT) parent-child intervention for 4-7-year-old children at risk for anxiety disorders. The 20-session intervention was first piloted openly in 9 children (between 3/10/98 and 1/1/2001). The intervention was then tested in 65 children in a randomized controlled trial versus a monitoring-only wait-list control condition. Children had to either have an anxiety disorder, behavioral inhibition, or be the offspring of a parent with an anxiety disorder who had elevated symptoms of anxiety. In practice all children but one had at least one anxiety disorder at baseline. Children were blocked on presence or absence of parental anxiety disorder and randomized to the intervention or to a no-intervention wait-list control group. The intervention consisted of 6 parent-only sessions, 8-13 child-parent sessions, and a final parent session. Post-trial assessments were conducted at six months, and at one-year follow-up. The hypotheses were that the children assigned to the intervention group would show significantly better improvement (measured via Clinician Global Impression-Anxiety Improvement scale and absence of anxiety disorders) than children assigned to the wait-list condition.