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Fatigue clinical trials

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NCT ID: NCT02205853 Recruiting - Cancer Clinical Trials

Implementation of Physical Cancer Rehabilitation Programmes in a European Healthcare System.

Start date: n/a
Phase: N/A
Study type: Interventional

The aim of this study is to develop and identify the most effective strategy to implement PCRPs into daily care. We want to assess the added value of a multi-faceted strategy compared with a single-faceted patient-directed strategy.

NCT ID: NCT02127268 Recruiting - Quality of Life Clinical Trials

Thymosin-α1 in Cancer-Related Fatigue

Start date: April 2014
Phase: Phase 3
Study type: Interventional

Cancer-related fatigue (CRF) is a distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportion to recent activity and interferes with usual functioning. Compared with general fatigue, CRF have the characteristics of long duration and generally cannot alleviate by rest or sleep, serious impact on the patient's work, study, entertainment and family life, and thus greatly affect the recovery, self-care ability and life quality of patients. Many dates showed that 70%~100% of cancer patients experienced cancer-related fatigue.For cancer-related fatigue there is no good treatment and intervention, in recent years, many clinical trials are carried out; central nervous stimulant, such as methylphenidate; acupuncture, aerobic exercise. All those measures may have certain therapeutic effect for CRF, but don't have exact evidences from massive RCT to confirm. Thymosin-α1 (T-α1), a synthetic 28-amino acid peptide with multiple biological activities primarily directed towards immune response enhancement, this drug is used for the treatment of HBV and hepatitis C virus (HCV) infections, and being developed for the treatment of non-small cell lung cancer (NSCLC), hepatocellular carcinoma, AIDS and malignant melanoma. T-α1 is able to potentiate the action of cytokines and also reduce the hematological toxicity of cytotoxic drug therapy, such as cyclophosphamide, 5-fluorouracil, dacarbazine. In this studies, we want to demonstrated that the effectiveness of Thymosin-α1 for cancer-related fatigue in cancer patients who undergo chemotherapy.

NCT ID: NCT02126891 Recruiting - Clinical trials for Muscle; Fatigue, Heart

FACEFI : Cardiac Fatigue During Intense Exercises - Pilot Study

FACEFI
Start date: January 2014
Phase: N/A
Study type: Interventional

To attest if a cardiac fatigue appears (and to measure it if it does) during intense physical exercises in two groups of subjects: - Canoeists from a training center of the French canoeing team during an intensive session of three weeks of endurance training; - Young recruits in military school of officers in ground forces of the French army during an intensive.

NCT ID: NCT02041364 Recruiting - Breast Cancer Clinical Trials

Biomarkers of Fatigue Related to Adjuvant Chemotherapy for Breast Cancer

Start date: November 2013
Phase: N/A
Study type: Observational

Fatigue is common in cancer patients receiving adjuvant chemotherapy. To further understand the mechanism of fatigue and search for potential biomarkers, we will conduct a prospective study with breast cancer patients receiving adjuvant chemotherapy.

NCT ID: NCT01926132 Recruiting - Chronic Fatigue Clinical Trials

High-dose Ascorbic Acid Intravenous Injection Decreases Mitochondrial DNA Damage in Chronic Fatigue Patients: Randomized-controlled Study

Start date: August 2013
Phase: Phase 4
Study type: Interventional

Reactive Oxygen Species (ROS) can cause oxidative damage, resulting in oxidation of lipids, proteins and DNA. In fatigue patients, there are some evidences of oxidative damage to DNA. Ascorbic acid was known to protect mitochondrial injury against oxidative stress by depolarizing the mitochondrial membrane. The copy number of mitochondrial DNA(mtDNA) was suggested mitochondrial gene stability and biogenesis and reflected mitochondrial function. There is no evidence ascorbic acid would decrease the mtDNA damage in fatigue patients. The investigators hypothesized that decreasing in mtDNA copy number in salivary and blood sample may be reversed by high-dose vitamin C intravenous injection in fatigue patients. The investigators will compare the mtDNA copy number and fatigue scale between moderate-severe fatigue patients and control group that had not malignant and chronic illness by a randomized controlled trial.

NCT ID: NCT01907711 Recruiting - Clinical trials for Cognitive Impairment

Clinical Trial to Evaluate the Effectiveness of Acupuncture as a Treatment in Patients Diagnosed With CFS.

AV/AS
Start date: February 2013
Phase: Phase 2/Phase 3
Study type: Interventional

background: The Chronic Fatigue Syndrome (CFS) presents many disturbances multidimensional affect holistically to people who have the disease and current management of fatigue, pain, anxiety, depression and sleep disturbances present in this clinical entity is unsatisfactory. Hypothesis: The hypothesis of this essay is to contrast that acupuncture is more useful than placebo. The investigators suggest the use of a clinical study protocol (PEC), randomized, placebo-controlled, acupuncture technique, aimed at increasing the patient's sense of well-being, relief of pain and stiffness, acupuncture is effective to reduce fatigue, anxiety, depression and sleep disorders in patients diagnosed with CFS.

NCT ID: NCT01893619 Recruiting - Clinical trials for Chronic Fatigue Syndrome

Observational Research on Use of Immunoprop Supplement in Chronic Fatigue Syndrome

immunoprop
Start date: June 2013
Phase: N/A
Study type: Observational

Observational study regarding the use of supplements in chronic fatigue syndrome patients

NCT ID: NCT01879202 Recruiting - Multiple Sclerosis Clinical Trials

Methylphenidate as Treatment Option of Fatigue in Multiple Sclerosis

MS
Start date: December 2012
Phase: Phase 2
Study type: Interventional

Fatigue is a common symptom in multiple sclerosis (MS) that is characterized by physical and/or mental exhaustion. Fatigue is difficult to treat and treatment efficacy of available therapy is limited. The goal of this study is to determine whether MS-associated fatigue improves after 6 weeks of methylphenidate therapy. Treatment efficacy will be measured by a questionnaire called "Fatigue Severity Scale" (FSS).

NCT ID: NCT01793415 Recruiting - Clinical trials for Chronic Fatigue Syndrome

Treatment of Chronic Fatigue Syndrome (CFS) With Iodinated Activated Charcoal (IodoCarb®)

Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Chronic fatigue syndrome (CFS) is a devastating and complex disorder. People with CFS experience overwhelming fatigue and a host of other symptoms that are not improved by bed rest. Interestingly, many of the symptoms experienced by people with CFS are identical to symptoms caused by long-term low-level exposure to mercury, which is called micromercurialism. This study will examine if the mercury binding substance IodoCarb(r) can improve the health of patients with CFS.

NCT ID: NCT01764620 Recruiting - Muscle Fatigue Clinical Trials

Effects of Muscle Fatigue and a Taping Technique on Shoulder Motion of Athletes

Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effects of muscle fatigue in the scapular kinematics of overhead athletes with and without using a kinesio taping technique for facilitating lower trapezius function. The hypothesis is that the taping technique could compensate for the negative effects caused by muscle fatigue in the scapular kinematics of healthy overhead athletes.