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Fatigue clinical trials

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NCT ID: NCT00860236 Completed - Clinical trials for Chronic Fatigue Syndrome

Giardia Induced Fatigue and Functional Gastrointestinal Diseases

GIFF
Start date: March 2009
Phase: Phase 4
Study type: Interventional

A giardiasis outbreak in Bergen has given us the opportunity to approach two basic research questions of national and global importance: - Studying the pathoimmunology of giardiasis in a natural setting, and following the genetic and immunological responses leading to recovery or persistent disease and sequelae. - Studying the two disease entities FGID and CFS when induced by acute giardiasi and their risk factors. - Interventional cognitive behavioural therapy is the only intervention documented to have significant effect on CFS outcome, and conventional cognitive behavioural therapy will be compared to a psycho-educational programme in the format of a randomised controlled trial.

NCT ID: NCT00852111 Completed - Cancer Clinical Trials

Molecular-Genetic Correlates of Fatigue in Cancer Patients Receiving Localized External Beam Radiation Therapy

Start date: April 23, 2009
Phase:
Study type: Observational

Background: - Researchers have studied the causes of fatigue during treatments for various diseases, but these results have not been conclusive. - More information on the physical changes that affect the body during treatment may help identify biological or chemical factors that contribute to patient fatigue, which may allow physicians to identify individuals who may be more at risk of feeling fatigue before, during, and after treatment for diseases such as cancer. Objectives: - To identify factors contributing to fatigue in men who are undergoing radiation treatment for prostate cancer. Eligibility: - Men 18 years of age and older who are scheduled to receive localized radiation treatment for prostate cancer. Design: - Six outpatient visits to the NIH Clinical Center, approximately on the same day and same time of day: - First visit before beginning radiation treatment. - Once a week for the first 2 weeks of the treatment, once at the midpoint of treatment, once at the end of treatment. - Final visit 4 weeks after completion of radiation treatment. - Initial visit will involve a physical examination and questions about medical history. - Evaluations during the treatment period: - Blood draws to identify cells and chemicals associated with inflammation and fatigue. - Questions about physical activity, fatigue, depression, and quality of life.

NCT ID: NCT00851812 Completed - Fatigue Clinical Trials

Exercise for Breast Cancer Patients (EXCAP)

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

The purpose of this study is to examine if exercise helps improve cancer-related fatigue. Hypothesis: A structured home-based walking and progressive resistance exercise program will be efficacious in relieving cancer-related fatigue, preventing aerobic and anaerobic deconditioning and skeletal muscle wasting, as well as improving inflammatory cytokine profiles in breast cancer survivors as well as those receiving radiation treatment.

NCT ID: NCT00848692 Completed - Clinical trials for Chronic Fatigue Syndrome

Drug Intervention in Chronic Fatigue Syndrome

KTS-1-2008
Start date: June 2008
Phase: Phase 2/Phase 3
Study type: Interventional

Based on pilot patient observations,the investigators anticipate that chronic fatigue syndrome (CFS) patients may benefit from B-cell depletion therapy. The hypothesis is that at least a subset of CFS patients have an activated immune system involving B-lymphocytes, and that B-cell depletion may alleviate symptoms.

NCT ID: NCT00840554 Completed - Fatigue Clinical Trials

The Effects of Adding a Home Exercise Program to a Clinical Physical Therapy Program on Cancer-Related Fatigue

Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if adding a home exercise program to a clinic physical therapy program will improve the fatigue experienced by patients being treated with concurrent chemotherapy and radiation therapy for high grade gliomas.

NCT ID: NCT00825682 Completed - Clinical trials for Radiation Related Fatigue

The Effect of Reflexology on Radiation-Related Fatigue in Breast Cancer Patients

Start date: May 2008
Phase: Phase 1/Phase 2
Study type: Interventional

Oncologic patients often report increased fatigue during and after radiation therapy. Reflexology treatment has been demonstrated to alleviate symptoms of fatigue, nausea, and anxiety in oncologic patients treated with chemotherapy. The aim of the study is to evaluate the effect of reflexology on fatigue, quality of life, and quality of sleep of breast cancer patients during and after radiation therapy.

NCT ID: NCT00821067 Completed - Fatigue Clinical Trials

The Effect of Oral D-Ribose in "Baby Boomers" With Fatigue. A Randomized, Double-Blind Study

Start date: January 2009
Phase: N/A
Study type: Interventional

D-ribose, a natural occurring pentose carbohydrate, has repeatedly shown to enhance high-energy phosphates and improve function following ischemia, states of congestive heart failure, and recently in subjects with lung disease. An initial preliminary, open label pilot study demonstrated a positive benefit of D-ribose in "Baby-Boomer" subjects aged 50 to 65 years old complaining of persistent fatigue. The objective of this study will build on the previously collected data to evaluate oral D-ribose vs. dextrose (administered as a supplement) in relatively healthy, yet fatigued subjects with a goal of improving their state of fatigue.

NCT ID: NCT00815672 Completed - Fatigue Clinical Trials

Exercise for Prostate Cancer Patients

EXCAP
Start date: December 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to gain a better understanding of the mechanisms responsible for cancer-related fatigue.

NCT ID: NCT00810329 Completed - Fibromyalgia Clinical Trials

Proteomics of Cerebrospinal Fluid in Chronic Fatigue Syndrome

Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this study is: 1. To identify specific set of proteins in the cerebrospinal fluid (fluid surrounding the brain and the spinal cord), that are believed to be seen in Chronic fatigue syndrome (CFS) patients, but not in healthy controls (HC). A similar study that the investigators had conducted before,suggested that significant changes in proteins in the cerebrospinal fluid may be due to the fundamental pathology of this disorder. 2. Increased cerebrospinal fluid pressure (pressure that helps the cerebrospinal fluid to move around the brain and the spinal cord), may be related with certain symptoms like headache, sleep problems, light headedness, increased pain, excessive tiredness (fatigue) even with minimal work and memory problems. 3. Assessment of Autonomic Nervous system function (Sympathetic nervous system)between the CFS and HC. 4. Perform Lung Function Testing or pulmonary function test to estimate the lung capacities and score shortness of breath while performing breathing maneuvers. 5. Dolorimetry (18 tender point test) for assessment of pain threshold. 6. Capsaicin skin test 7. Allergy skin test

NCT ID: NCT00801346 Completed - Leukemia Clinical Trials

Metabolic Syndrome in Young Patients With Acute Lymphoblastic Leukemia in Remission

Start date: November 2008
Phase: N/A
Study type: Observational

RATIONALE: Gathering information about metabolic syndrome from young patients with acute lymphoblastic leukemia may help doctors learn more about the disease. PURPOSE: This phase I trial is studying the metabolic syndrome in young patients with acute lymphoblastic leukemia in remission.