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Mental Health clinical trials

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NCT ID: NCT00208715 Completed - Major Depression Clinical Trials

Provigil in Conjunction With SSRIs for the Treatment of Mild or Moderate Depression With Attendant Symptoms of Sleepiness and Fatigue.

Start date: February 2003
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to determine if Provigil® (modafinil) at a dose of 200 mg once daily is safe and effective for treating symptoms of sleepiness and fatigue associated with Major Depressive Disorder when added to a SSRI.

NCT ID: NCT00183352 Completed - Bipolar Disorder Clinical Trials

Reproductive Function and Mood in Women With Bipolar Disorder

Start date: January 2004
Phase: N/A
Study type: Observational

This study will determine the effect of medication for bipolar disorder on the reproductive function and whether mood changes occur during the menstrual cycle in women with bipolar disorder.

NCT ID: NCT00118833 Completed - Anxiety Disorders Clinical Trials

St. John's Wort for the Treatment of Generalized Social Anxiety Disorder (GSAD)

Start date: August 2002
Phase: Phase 2/Phase 3
Study type: Interventional

This study will determine whether the herbal product St. John's wort is safe and effective in treating generalized social anxiety disorder (GSAD). Study hypothesis: Hypericum perforatum (St. John's wort) is more effective in treating GSAD than placebo.

NCT ID: NCT00118534 Completed - Clinical trials for Tobacco Use Disorder

Integrating Clinical Practice Guidelines for Smoking Cessation Into Mental Health Care for Veterans With Posttraumatic Stress Disorder

Start date: July 2004
Phase: N/A
Study type: Interventional

The primary study objective is to conduct a prospective, randomized controlled clinical trial that compares the effectiveness of two approaches for delivering smoking cessation treatment for veterans with posttraumatic stress disorder (PTSD). An approach where smoking cessation treatment is integrated into mental health care for PTSD and delivered by mental health providers (experimental condition) will be compared to specialized smoking cessation clinic referral (VA's usual standard of care). Secondary study objectives are to (a) compare the cost outcomes and cost-effectiveness of IC versus USC, (b) identify treatment process variables that explain (mediate) observed differences in smoking abstinence rates for the two study conditions, and (c) determine whether cessation from smoking is associated with worsening of symptoms of PTSD and/or depression.

NCT ID: NCT00118391 Completed - Mental Health Clinical Trials

Cognitive-Behavioral Treatment of Gambling

CBT/CM
Start date: November 2002
Phase: Phase 1
Study type: Interventional

This study will determine the effectiveness of cognitive behavior therapy (CBT) and contingency management (CM) in reducing gambling behaviors and other related problems in pathological gambling. Study hypothesis: Participants who receive CBT and CM will attend more treatment sessions and show better outcomes than those who receive CBT alone.

NCT ID: NCT00055081 Completed - Mental Health Clinical Trials

The Impact of Family CTI on Homeless Children

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

The purpose of this study is to examine how services and housing provided for homeless families affect the mental health and behavior of homeless children over time.

NCT ID: NCT00034892 Completed - Schizophrenia Clinical Trials

CAFE Comparison of Atypicals in First Episode of Psychosis

Start date: March 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness, tolerability, and efficacy of the currently available atypical antipsychotic drugs olanzapine (2.5-20 mg/day), quetiapine (100-800 mg/day) and risperidone (0.5-4 mg/day) in patients with schizophrenia, schizophreniform disorder, or schizoaffective disorder who are experiencing their first psychotic episode.