Department of Veterans Affairs

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Pregnenolone for Cognitive and Negative Symptoms in Schizophrenia

Trial phase: 
Phase II
Recruitment status: 
Not yet recruiting

This study will investigate adjunction pregnenolone for cognitive symptoms and negative symptoms in patients with schizophrenia and schizoaffective disorder.

Background information
Trial ID: 
NCT00728728
Other unique IDs: 
MHBB-012-07F
Official title: 

Pregnenolone for Cognitive and Negative Symptoms in Schizophrenia

Detailed description: 

 

Number to be enrolled: 
88 patients

Aripiprazole for Methamphetamine Dependence: Double Blind Placebo Trial

The purpose of this study is to test whether treatment with Aripiprazole leads to a reduction in methamphetamine craving and use in patients diagnosed with methamphetamine dependence. Patients presenting at the Omaha VA Medical Center for treatment of methamphetamine dependence, and meet inclusion criteria for the study will be invited to participate. Participation in the study will last for approximately 14 weeks.

Background information
Other unique IDs: 
CDA-2-017-08S

Evaluation of Open-Canal Behind-the-Ear Hearing Aids and Traditional In-the-Ear Hearing Aids.

Recruitment status: 
Not yet recruiting

This study is being conducted to evaluate the benefits of in-the-ear vs. open-fit behind-the-ear hearing aids. We want to learn more about which patients prefer each type, so we can make better choices about which type of hearing aid is best for which patients. Participants in this study will try three different sets of hearing aids for 2 months each, then we will evaluate the benefit of each type.

Background information
Trial ID: 
NCT00727909
Other unique IDs: 
C6288R
Official title: 

Evaluation of Open-Ear Canal and Traditional Custom-Fit Hearing Aids

Detailed description: 

Hearing loss is the most common service-connected disability nationwide in the VHA system, with hearing aids providing the primary treatment option. Although the benefits of hearing-aid use are clearly established,~16-30% of adults who have hearing aids do not use them. Several factors are believed to result in non-use of traditional hearing aids, including (1) poor fit and comfort, (2) poor cosmetics, (3) whistling feedback, (4) occlusion, and (5) difficulty understanding speech in noise.

Number to be enrolled: 
288 patients

Study of Individualized Wound Prevention Instruction to Prevent Venous Ulcer Development

Trial phase: 
Phase I
Recruitment status: 
Active, not recruiting

The purpose of this study is to determine whether individualized wound prevention instructions will lengthen the ulcer-free period in veterans with recently healed venous ulcers.

Background information
Trial ID: 
NCT00727701
Other unique IDs: 
08-246
Official title: 

Does Use of a Wound After-Care Summary for Patients With a History of Venous Ulcers Lower Recurrence Rate?

Detailed description: 

Venous ulcer disease is the most common form of lower extremity ulcer, and treatment requires months to years of costly intervention. Preventing venous ulcers from recurring is ideal, however, healing time is variable, possibly due to inadequate patient/clinician communication and surveillance. An aftercare summary is a detailed set of self-care instructions designed to help patients understand and influence preventative factors under their control. They have successfully been used in patients with cardiac disease and are currently being tested to help prevent diabetic foot ulcers.

Number to be enrolled: 
72 patients

Efficacy and Mechanisms of Pharmacologic Treatment of Fecal Incontinence

The purpose of this study is to evaluate and compare treatment with fiber and loperamide for fecal incontinence.

Background information
Other unique IDs: 
B6126W

Supplementing Hearing Aids With Computerized Auditory Training

Recruitment status: 
Recruiting

The study is designed to examine the effectiveness of a computer-based auditory training program to improve the benefits received by individuals who wear hearing aids. The study will involve 3 groups - a computer-based training group, an active listening group which will involve listening to books on CD, and a placebo group that receives no additional treatment.

Background information
Trial ID: 
NCT00727337
Other unique IDs: 
C6303R
Official title: 

Supplementing Hearing Aids With Computerized Auditory Training

Detailed description: 

This proposed study is a multi-site, single-masked (blinded), randomized controlled, parallel group clinical trial to assess the effectiveness of an at home PC-based auditory training as a supplement to standard-of-care hearing-aid intervention in veterans treated for hearing loss, with or without previous hearing-aid experience.

Number to be enrolled: 
288 patients
Acronym: 
LACE

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

Validation of Brief Objective Neurobehavioral Detectors (BOND) in Mild TBI

The Veterans Health Administration (VHA) has stated the need for a brief screening instrument that can assist with the triage of the enormous number of returning OIF/OEF veterans with concussion. The investigators combined selected neurological and brief cognitive tests to develop an instrument called, "Pincus Repeatable Objective Neurobehavioral Evaluation" (PRONE). PRONE takes only 15-20 minutes to administer with immediate results. In a previous study, PRONE was able to predict periventricular white matter disease (PWMD) visible on MRI scans with 91% sensitivity and 76% specificity. Thus, PRONE has shown sensitivity to, and specificity for, white matter abnormalities. Given that white matter abnormalities are the most common type of injury in mTBI, it is probable that PRONE could be sensitive to traumatic axonal injury (TAI) in TBI. Advanced neuroimaging measures, such as diffusion tensor imaging, will be used to help validate PRONE. If validated as a screening tool for OIF/OEF veterans with concussion, PRONE could reduce evaluation and associated waiting times and accelerate the initiation of treatment or case management. These benefits would be expected to increase veteran quality of life and satisfaction with care.

Background information
Other unique IDs: 
SHP 08-167
01133

PC-Based Rehabilitation of Auditory Function

Many older subjects experience difficulty in understanding speech in noisy environments. Part of this problem is related to changes that occur in the ear with age and compromise the hearing of high-pitched sounds. Another part of the problem with speech understanding relates to changes with age in the neural circuits of the brain that process different speech sounds. Evidence suggests that these changes in neural circuits are particularly large if hearing loss is present. Thus, while hearing aids may help compensate for hearing deficits by amplifying speech sounds, additional treatment is necessary to restore optimal neural connections in the brain so that speech sounds can be accurately distinguished from each other. We are developing PC-based training programs in an attempt to restore optimal neural connections. The current randomized trial will evaluate whether two months of training to improve the ability to discriminate different consonant sounds in noise will also improve the understanding of continuous speech and enhance auditory memory and other high-level auditory functions.

Background information
Other unique IDs: 
C4739R

Telephone Care Coordination for Smokers in VA Mental Health Clinics

Recruitment status: 
Not yet recruiting

The purpose of this study is to evaluate whether a smoking cessation telephone care coordination program is effective and feasible in VA Mental Health Clinics.

Background information
Trial ID: 
NCT00724308
Other unique IDs: 
SDP 07-034
Official title: 

Telephone Care Coordination for Smokers in Mental Health Clinics

Detailed description: 

Smoking is the leading preventable cause of death in the United States and is a particular problem among VA users and among persons with a diagnosed mental illness. The prevalence of smoking among VA mental health patients has remained high, in part because smoking cessation treatment rates have remained low. Telephone-based counseling represents the most feasible approach to increasing smoking cessation treatment among VA patients. The approach used in this study has been used very effectively in a primary care-based population that includes a large percentage of mental health patients.

Number to be enrolled: 
10000 patients
Acronym: 
TeleQuit MH
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