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Mental Health clinical trials

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NCT ID: NCT00598884 Completed - Mental Health Clinical Trials

Effectiveness of an Internet-Based Self-Management Program in Treating Prolonged Grief Disorder

Start date: August 2009
Phase: Phase 1
Study type: Interventional

This study will evaluate the effectiveness of an Internet-based self-help program in treating people who are at risk for developing prolonged grief disorder following a recent loss.

NCT ID: NCT00577811 Completed - HIV Infections Clinical Trials

Evaluation of Enrollment, Dynamics of Care and Patient Outcomes in the NYS Medicaid HIV Special Needs Plans

Start date: February 2003
Phase: N/A
Study type: Observational

The purpose of this study is to find out how people's needs are being met and what people do about problems with treatment, symptoms, substance use, mental health, and social services. We are also interested in finding out about changes that people make in their health care team and the reasons for making those changes.

NCT ID: NCT00534482 Completed - Physical Activity Clinical Trials

Evaluation of the "Americans in Motion - Healthy Interventions" Project

AIM-HI
Start date: July 2007
Phase: N/A
Study type: Interventional

This research project brings together the American Academy of Family Physicians (AAFP) National Research Network (AAFP-NRN) and the AAFP's public health initiative, Americans In Motion (AIM). This project will develop and evaluate a practice improvement program to improve family physicians' delivery of effective patient-centered behavior change interventions for "fitness" (physical activity, nutrition and emotional well-being). The investigators seek to develop a unique program that positions fitness in a central role as "the treatment of choice" when dealing with issues of prevention and treatment of chronic conditions. In addition, this newly developed program is intended to help shift the paradigm of family physicians' use of common advice-giving methods to more effective patient-centered lifestyle counseling. Ultimately, this program will seek to improve care for all patients through fitness-related physician interventions. Outcomes: This study design will allow the investigators to evaluate whether (and how) dissemination of educational materials impacts patient intervention by first engaging clinicians and staff in their personal use of these materials. This project will also evaluate the effects of the behavioral change tools, as well as, the added impact of new physiologic feedback measures (HOMA-IR and NMR Lipoprotein profiles) on physical activity and diet in study participants. Conclusion: Primary care offices can become more effective settings to help patients improve physical activity, diet and emotional well-being. Demonstrating the value and impact of creating "healthy offices" that endorse and support clinicians, office staff and patients in the use of effective educational materials fits well with the new model of care as part of the AAFP's "Future of Family Medicine" initiatives, which emphasize the importance of lifestyle decisions and supporting successful changes in behaviors within primary care. This project will help define how to accomplish this.

NCT ID: NCT00482001 Completed - Mental Health Clinical Trials

Impact of Cholinesterase Inhibitors on Driving Ability in Healthy Older Adults

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The goal of the study is to assess the role of cholinesterase inhibitors in affecting the driving ability of cognitively intact seniors using driving simulators. We hypothesize that the use of a cholinesterase inhibitor for two weeks will be associated with improvement in safe driving behavior on a simulated driving task.

NCT ID: NCT00479271 Completed - Dementia Clinical Trials

Evaluating the Effectiveness of a Community Based Intervention for Persons With Dementia and Their Caregivers in a Developing Country

Start date: October 2003
Phase: N/A
Study type: Interventional

The aim of this trial was to apply a home based, flexible, stepped-care intervention designed to improve the awareness and knowledge of family caregivers regarding dementia, to maximise their caregiving resources and to improve their caregiving skills. A Randomized Controlled Trial (RCT) will be used to evaluate the same wherein the intervention group will get the services immediately and the control arm would receive the same after a period of 6 months.

NCT ID: NCT00296140 Completed - Mental Health Clinical Trials

Implementing Evidence in the Detection and Treatment of Post Stroke Depression

Start date: December 13, 2006
Phase: N/A
Study type: Interventional

Post Stroke Depression (PSD)is a high volume condition with negative impact on patient recovery after stroke. The primary aim of this study is to evaluate the effectiveness of a system intervention to improve the proportion of Veterans screened and started on treatment for PSD. The secondary aim is evaluate whether a patient-based self-management intervention provides any additional benefit compared to usual care.

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.