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Persian Gulf Syndrome clinical trials

View clinical trials related to Persian Gulf Syndrome.

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NCT ID: NCT01291758 Completed - Gulf War Illness Clinical Trials

Exercise in Gulf War Illness (GWI)

Start date: July 2009
Phase:
Study type: Observational

The purpose of this study is to determine if submaximal exercise by bicycle stress tests with pulmonary measurement of VO2MAX plus maximal isometric hand grips on 2 consecutive days causes a higher level of "exertional exhaustion" in GWI compared to healthy veterans (HVets).

NCT ID: NCT01267045 Completed - Clinical trials for Persian Gulf Syndrome

Mindfulness-Based Stress Reduction for Gulf War Syndrome

Start date: October 2010
Phase: N/A
Study type: Interventional

This pilot study is a two arm randomized, controlled clinical trial that evaluated whether a standardized Mindfulness-Based Stress Reduction (MBSR) intervention reduces symptoms associated with Gulf War Syndrome (GWS) more effectively than treatment as usual. Fifty-five veterans meeting diagnostic criteria for Gulf War Syndrome were randomized to treatment as usual (TAU) or TAU plus an 8-week course of course of MBSR. Study measures were collected at baseline, immediate post-MBSR, and 6 months post intervention. Measures were obtained at equivalent time points for veterans randomized to TAU only. Following completion of all study activities, veterans randomized to TAU only had the opportunity to enroll in MBSR.

NCT ID: NCT01264471 Completed - Gulf War Syndrome Clinical Trials

Mechanisms of Mitochondrial Defects in Gulf War Syndrome

Start date: May 2009
Phase: N/A
Study type: Observational

The purpose of the study is to investigate possible causes for Gulf War Syndrome. Gulf War Syndrome is associated with increased incidences of amyotrophic lateral sclerosis (Lou Gehrig's Disease), pain syndromes, muscle complaints that include fatigue and myalgias (muscle pain), as well as other neurological symptoms. Abnormalities in the part of the cell known as mitochondria have been delineated in Gulf War Syndrome. Mitochondria are the "power plants" of the body. Mitochondria take the food you eat and break the food down into a form of energy that the body can use. The investigators propose that Gulf War Syndrome is determined by a complex interaction of factors that interfere with mitochondrial function. This study will be the first investigation of mitochondrial function in Gulf War Syndrome. The investigators objective is to establish the cause for symptoms in affected veterans, develop testing that can more easily identify Gulf War Syndrome, and ultimately develop treatment protocols for Gulf War Syndrome.

NCT ID: NCT00810368 Completed - Clinical trials for Persian Gulf Syndrome

Treatment Study of Carnosine Versus Placebo in Gulf War Illness (GWI)

Start date: August 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to perform a randomized double-blind, placebo-controlled, 12 week study of the effects of carnosine on cognitive, psychometric, autonomic, and muscle strength outcomes in 100 GWI subjects.

NCT ID: NCT00810225 Completed - Gulf War Illness Clinical Trials

Study of Gulf War Illness (GWI) by Comparing GWI and Healthy Veterans

Start date: August 2008
Phase:
Study type: Observational

Determine if: - genetic differences of CNDP1 gene - the previously defined GWI/Chronic Fatigue Syndrome (GWI/CFS) cerebrospinal fluid proteome contents - psychometric - other variables can differentiate between veterans of the 1990-1991 Persian Gulf War who have autonomic, neurological and other symptoms and those without these complaints.

NCT ID: NCT00568555 Completed - Fibromyalgia Clinical Trials

Effects of Low Dose Naltrexone in Fibromyalgia

Start date: June 2007
Phase: N/A
Study type: Interventional

Low Dose Naltrexone (LDN) has been reported anecdotally to reduce the symptoms of Fibromyalgia, a Chronic Multisystem Illness. The drug may work by regulating natural pain-reducing systems. In this study, we will administer both LDN and placebo to a small group of individuals with Fibromyalgia and Gulf War Syndrome, both Chronic Multisymptom Illnesses, to assess the drug's efficacy in treating the condition.

NCT ID: NCT00129454 Completed - Gulf War Syndrome Clinical Trials

Telemedicine Treatment for Veterans With Gulf War Illness

Start date: September 1, 2005
Phase: N/A
Study type: Interventional

Effective treatments have been developed to ameliorate symptom-related distress and reduce unnecessary healthcare utilization using cognitive-behavioral techniques (CBT) . However there is a major limitation of this treatment is that patients must attend sessions in person. The specific aims of the study are to: (1) Determine the clinical efficacy of Telephone CBT for veterans with GWI who are frequent consumers of ambulatory medical care; (2) Determine whether CBT for veterans with GWI leads to a reduction in the cost of VA health care; and (3) Develop a statistical model of treatment seeking in veterans with GWI who are frequent consumers of ambulatory medical care.

NCT ID: NCT00100412 Completed - Clinical trials for Post-Traumatic Stress Disorder

Hyporeactivity and Gulf War Illness

Start date: October 1999
Phase: N/A
Study type: Interventional

This research project is a follow-up to the prior VA-funded study that found that chronic fatigue reported by many Gulf War veterans may be a symptom of dysfunctional cardiovascular stress response regulation. Specifically, ill veterans had diminished autonomic responses during demanding psychosocial tasks involving high level cognitive processing and emotional stress. There was a close relationship between clinical status of ill veterans and their inability to mount an appropriate physiological response under stress. The main objective of the present investigation is to determine the specific mechanism through which this abnormality may contribute to Gulf War-related chronic fatigue. We also observed that Gulf veterans with posttraumatic stress disorder (PTSD) had the most dampened autonomic activation to stressors involving higher brain activities. The second major focus of this study is to explore the role of a psychiatric disorder, specifically PTSD, as a factor in abnormalities in stress response regulation. This aspect of the study may also provide pertinent information as to the role of stress of military deployment as a contributing factor in post-Gulf War illnesses.

NCT ID: NCT00018707 Completed - Gulf War Syndrome Clinical Trials

Follow-up of Psychological and Neurocognitive Gulf War Outcome: Relation to Stress

Start date: April 1999
Phase: N/A
Study type: Observational

This is the follow-up to an observational epidemiological study of psychological and neuropsychological outcomes of deployed and non-deployed Gulf War-era veterans.

NCT ID: NCT00007748 Completed - Clinical trials for Persian Gulf Syndrome

Exercise and Behavioral Therapy Trial (EBT).

Start date: March 1999
Phase: Phase 3
Study type: Interventional

This trial is a study of Gulf War era veterans who have unexplained chronic medical symptoms such as pain, fatigue, and/or cognitive difficulties. The treatments to be studied, cognitive behavior therapy (CBT) and aerobic exercise, have been shown to be effective in alleviating symptoms in individuals with other similar types of illnesses, such as chronic fatigue syndrome and fibromyalgia. This is a Phase 3, 2X2 factorial designed study. All study participants are assigned to one of four treatment groups - CBT and aerobic exercise, aerobic exercise alone, CBT alone or usual and customary care. This study durations is 28 months; 1092 participants were enrolled and will be followed in clinic at 3, 6 and 12 months after enrollment.