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Fatigue clinical trials

View clinical trials related to Fatigue.

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NCT ID: NCT02495428 Completed - Muscle Fatigue Clinical Trials

Effect of Kinesio Taping in Muscle Fatigue

Start date: January 2015
Phase: N/A
Study type: Interventional

The aim of this study was to determine the effect of Kinesio taping on lactic acid in an running anaerobic test.

NCT ID: NCT02495155 Completed - Breast Cancer Clinical Trials

Initial Assessment of an Internet-based Symptom Management Intervention in Early Stage Breast Cancer

PROSPECT
Start date: June 2015
Phase: N/A
Study type: Interventional

In order to determine the acceptability of a breast cancer-specific cognitive behavioral therapy intervention, as well as to obtain preliminary data to assess efficacy in managing symptoms, the investigators will ask 45 breast cancer survivors with moderate insomnia, fatigue, and/or pain to use the investigators' internet-based intervention for 8 weeks and to complete patient-reported outcomes assessments before and after the 8 week intervention.

NCT ID: NCT02489422 Completed - Depression Clinical Trials

Programs To Support You During Chemotherapy

PRO-YOU
Start date: August 2016
Phase: N/A
Study type: Interventional

This randomized pilot trial studies how well two supportive programs work for improving fatigue and depressive symptoms in patients with GI undergoing chemotherapy. Possible mediators such as psychological stress, circadian disruption, and inflammation, will also be explored.

NCT ID: NCT02475785 Completed - Clinical trials for Malocclusion, Angle Class II, Division 1

Evaluation of Mini Plates Anchorage With Forsus Fatigue Resistant Device

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the Forsus Fatigue resistant Device appliance with direct skeletal mini plates anchorage is capable of achievement of skeletal mandibular effects while preventing the excessive proclination of the lower incisors at the end of the treatment when compared to the conventional Forsus Fatigue resistant Device appliance applied to the upper and lower dental arches in female patients with skeletal Class II malocclusion

NCT ID: NCT02475486 Completed - Clinical trials for Rheumatoid Arthritis

Role of the ANS Dysregulation in the Persistence of Fatigue in Rheumatoid Arthritis Patients Treated With Anti-TNF

ANSRA
Start date: February 25, 2016
Phase: N/A
Study type: Interventional

Despite the large therapeutic arsenal available since one decade allowing a strong reduction of inflammation process, rheumatoid arthritis (RA) patients claimed pain, fatigue, sleep problems and other quality of life outcomes. Fatigue reduction during TNF blockers therapy is lower than the strong reduction in RA disease activity. Furthermore, RA patients have higher prevalence of non-inflammatory pain than general population. Fatigue is a real major problem due to 50% of patients considered it as severe. This dissociation between disease activity and fatigue level suggests that fatigue is multifactorial. No consistent explanations for fatigue are currently available.

NCT ID: NCT02474940 Completed - Multiple Sclerosis Clinical Trials

MS Symptom Management Study

ENHANCE
Start date: June 2015
Phase: N/A
Study type: Interventional

People with Multiple Sclerosis (MS) often have pain and/or fatigue. Unfortunately, available treatments provide inadequate relief for the majority of these individuals. There remains an urgent need for additional treatment options for MS-related symptoms. The purpose of this study is to see if alternative treatments that involve self-hypnosis training, neurofeedback training and/or mindfulness meditation training, or a combination of some of these treatments can help decrease pain and fatigue in people with MS. A subject must have a diagnosis of MS, have chronic pain and/or fatigue, and be at least 18 years old to participate, among other criteria.

NCT ID: NCT02444091 Completed - Clinical trials for Chronic Fatigue Syndrome (CFS)

Cyclophosphamide in Myalgic Encephalopathy/ Chronic Fatigue Syndrome (ME/CFS)

CycloME
Start date: March 2015
Phase: Phase 2
Study type: Interventional

Significant clinical improvements of ME/CFS symptoms were observed in two patients with long-standing ME/CFS who received adjuvant chemotherapy including cyclophosphamide for breast cancer, also in one ME/CFS patient who received chemotherapy including iphosphamide for Hodgkin lymphoma. Three pilot ME/CFS patients were thereafter treated with six intravenous infusions four weeks apart, in two of these with a significant clinical response. The hypothesis is that a subset of ME/CFS patients have an activated immune system, and that ME/CFS symptoms may be alleviated by treatment with cyclophosphamide as intravenous pulse infusions four weeks apart, six infusions in total. The purpose of the present study is to treat ME/CFS patients with cyclophosphamide as intravenous pulse infusions four weeks apart, six infusions in total. The effects on ME/CFS symptoms and tolerability/side effects during 12 months follow-up will be registered, and additional tests will be performed to objectively register changes in physical ability during follow-up. Studies to investigate possible large vessel endothelial dysfunction and skin microvascular dysfunction will be performed before start of intervention and during follow-up.

NCT ID: NCT02442635 Completed - Cancer Clinical Trials

Yoga During Chemotherapy Study

Start date: May 2015
Phase: N/A
Study type: Interventional

This proposal aims to expand non-pharmacologic options for the control of symptoms during chemotherapy using yoga practices. It is particularly focused on sleep disturbance with a secondary focus on fatigue.

NCT ID: NCT02435043 Completed - Stroke Clinical Trials

A Trial of Nature-based Post-stroke Fatigue Rehabilitation (NASTRU)

NASTRU
Start date: August 2012
Phase: N/A
Study type: Interventional

The aim of NASTRU was to examine whether ten weeks of nature-based rehabilitation, as add-on to standard management, could influence post-stroke fatigue (primary outcome), depression, work ability or functional outcome (secondary outcomes), compared to controls.

NCT ID: NCT02434367 Completed - Breast Cancer Clinical Trials

The Effect of Walking on Fatigue During Radiotherapy in Breast Cancer Patients 65 and Older

WWE
Start date: August 2014
Phase: Phase 2
Study type: Interventional

This multicenter randomized (1:1) phase 2 study is designed to assess the efficacy of the Walk with Ease exercise program on improving fatigue after adjuvant radiotherapy compared to usual care in 50 women with stage 0-3 breast cancer who have undergone breast surgery. Prior to initiation of radiation, during the last week, and 4-6 weeks post radiation, women in both arms will complete a number of surveys including questionnaires on fatigue, pain, depression, sleep, and social support. In addition, a blood sample will be collected prior to, during the last week of radiation, and 4-6 weeks post radiation to explore measures of inflammatory biomarkers, and their potential association with exercise and fatigue.