Depression

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Creatine Augmentation Treatment in Major Depressive Disorder Subjects

Recruitment status: 
Recruiting

Given 1) the established safety with short-term or long-term supplementation of Cr, 2) its potential usefulness in improving brain energy metabolism, 3) the reported abnormality in brain energy metabolism in MDD subjects, and 4) plausible association between depression and inflammatory mediators, we hypothesize that oral Cr augmentation will help reduce symptoms in MDD patients as well as normalize a deficit in brain energy metabolism and that improvement of MDD and brain energy metabolism will be correlated with inflammatory mediators changes. In this current study, we plan to conduct an randomized, double-blind, placebo-controlled augmentation study with creatine in addition to escitalopram for treating 50 MDD subjects. We will assess the efficacy and safety of the Cr augmentation and evaluate changes relevant to brain energy metabolism and inflammatory mediators.

Background information
Trial ID: 
NCT00729755
Other unique IDs: 
BIC-08DE00101B
Official title: 

Efficacy and Safety of Augmentation of Creatine for the Patients With Major Depressive Disorder

Detailed description: 

 

Number to be enrolled: 
50 patients

The Therapeutic Efficacy of Neurofeedback in Depression

The investigators examined the therapeutic efficacy of neurofeedback in depression subjects. The investigators hypothesize that 5 weeks neurofeedback training will be able to alleviate depressive symptoms.

Background information
Other unique IDs: 
KRF-2005-079-HS0012

Educational Needs of Patients Undergoing Watchful Waiting for Localized Prostate Cancer

RATIONALE: Gathering information about anxiety and depression in patients with localized prostate cancer who have selected watchful waiting may help doctors develop educational materials that help patients cope with cancer-related anxiety. PURPOSE: This study is looking at the educational needs of patients who are undergoing watchful waiting for localized prostate cancer.

Background information
Other unique IDs: 
CDR0000600452
BCM-H-19995

GSK372475 PK Study in Healthy Volunteers

This study will consist of 4 parallel cohorts of healthy volunteers(elderly male, elderly female, young male and young female. Subjects will receive either GSK372475 1.5mg or placebo for 28 days

Background information
Other unique IDs: 
105467

Adjusting to Chronic Conditions Using Education Support and Skills

Recruitment status: 
Recruiting

Medically ill patients with Congestive Heart Failure (CHF) and Chronic Obstructive Pulmonary Disease (COPD) are at increased risk for developing symptoms of anxiety and depression and are among the least frequent users of mental health services and treatments. To address the needs of chronically ill patients, we created a time-limited psychosocial intervention to maximize treatment benefits and improve the efficiency and ability of mental health care practitioners to provide services within medical care settings. This study is separated into two randomized study groups. The first group of participants will receive the ACCESS intervention immediately. The second group of participants will be followed for a period of 6 months. After a period of 6 months, those who continue to have symptoms of depression and/or anxiety will be offered the ACCESS intervention.

Background information
Trial ID: 
NCT00727155
Other unique IDs: 
H23264
Official title: 

Improving Quality Of Life For Chronically Ill Patients Using Education Support And Skills; A Randomized Controlled Mental Trial

Detailed description: 

 

Number to be enrolled: 
50 patients
Acronym: 
ACCESS

Effectiveness of a Technology Assisted Behavioral Intervention in Assisting People With Major Depressive Disorder

Trial phase: 
Phase I
Recruitment status: 
Not yet recruiting

This study will develop and evaluate the effectiveness of a technology-assisted behavioral intervention, consisting of Internet-based cognitive behavioral therapy combined with telephone and email support, in reducing depressive symptoms and improving treatment adherence in primary care patients with major depressive disorder.

Background information
Trial ID: 
NCT00719979
Other unique IDs: 
DSIR 83-ATP
R34 MH078922
Official title: 

Integrated Telemental Health Intervention for Depression in Primary Care

Detailed description: 

Major depressive disorder (MDD) is a common mental disorder, with up to 10.3% of the population experiencing the disorder in a given 12-month period. Symptoms of MDD include feelings of anxiety, guilt, or hopelessness; irregular sleep and appetite patterns; lethargy; excessive irritability and restlessness; inability to concentrate; and lack of enjoyment in previously enjoyed activities. Fortunately, MDD is treatable with forms of psychotherapy and/or antidepressant medications.

Number to be enrolled: 
70 patients

A Interventional Study of Geriatric Frailty, Osteoporosis, and Depression

Frailty, osteoporosis, and depression are three highly prevalent geriatric syndromes. Having these conditions are associated with adverse outcome in physical health, mental health, quality of life, and daily functioning. They are associated with higher mortality rates as well as increased health care cost. Risk factors, pathogenesis, clinical phenotypes, and interventions of these three geriatric syndromes are often related. Multifactorial, interdisciplinary integrated care models may benefit more to patients with the above 3 geriatric syndromes than single intervention targeting single condition. The objective of this proposed study is to conduct a randomized control trial (RCT) to exam the effectiveness of integrated interventions on multiple outcomes among community-dwelling Taiwanese elders with high risks for frailty, osteoporosis, or depression.

Background information
Other unique IDs: 
EC0970301

Efficacy of Narrative Exposure Therapy (NET) in Treating Women After Human Trafficking or Forced Prostitution

Recruitment status: 
Recruiting

The purpose of this study is to perform an evaluation of a trauma-focused short-term intervention (Narrative Exposure Therapy; Schauer, M., Neuner, F.

  • Elbert, T.) on a variety of clinical outcome measures (PTSD, Depression, Somatic Complaints, Dissociation) in women after sexual exploitation and women trafficking.

Background information
Trial ID: 
NCT00717548
Other unique IDs: 
FH05.06.2008
Official title: 

The Effectiveness of Narrative Exposure Therapy in Treating Women After Trafficking and Forced Prostitution

Detailed description: 

 

Number to be enrolled: 
10 patients

Epidemiology of Depression, Anxiety, and Cognitive Impairment

Many older adults have undetected health problems and lack basic prevention measures. Failure to identify and treat these conditions can lead to unnecessary morbidity and mortality and a decreased quality of life. Traditional screening and intervention programs, usually based in primary care providers' offices, have been insufficient, particularly in medically underserved populations. Alternate sites for screening and intervention have begun to receive attention and may hold promise. The emergency department (ED) is the entry point for access to medical and social services for many patients and has the potential to serve as a site to identify older adults with unmet needs. However, we do not know the prevalence of depression and cognitive impairment and how they differ by mode of arrival of the patient to the ED. Second, a question remains as to the validity of screening patients during an acute illness. Upon completion, this study will describe the epidemiology of the population of older adults presenting to the ED.

Background information
Other unique IDs: 
RSRB 24085
NIH 5K23AG028942

Does Fish Oil Prevent Depression in Pregnancy and Postpartum?

This study is designed to test whether an alternative medicine treatment, fish oil, will prevent depressive symptoms in pregnant and postpartum women who have been found to be at risk for depression. Epidemiologists have observed that people who live in countries where people on average eat a diet high in fish have a lower risk of depression than people who live in populations that eat less fish. Postpartum depression is also less common in these countries. The omega-3 fatty acids found in fish oil are thought to be responsible for this beneficial effect of eating fish. The two major omega-3 fatty acids found in fish are eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). DHA is an essential building block of the brain and nerve tissue. EPA may act to optimize the electrical signals between nerve cells and brain cells and may help the immune system to function well. Some researchers have treated people who are already suffering from depression with fish oil. Some of these studies have shown a benefit for the fish oil treatment and others have not. These studies have tested EPA and DHA alone and in various combinations. Currently, it is not known whether EPA or DHA is more effective in preventing and treating depression. Some of the researchers involved in this study have learned how to identify mothers who are most at risk for developing depression during and after pregnancy. This study is designed to learn whether EPA-rich and DHA-rich fish oil supplements will prevent depressive symptoms in women who are at risk to develop depression.

Background information
Other unique IDs: 
R21 AT004166-01A1
IRBMED# HUM00004684
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