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Fatigue clinical trials

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NCT ID: NCT02567669 Active, not recruiting - Breast Cancer Clinical Trials

Muscle Loss and Fatigue as a Consequence of Radiotherapy

MUSFAT
Start date: January 2016
Phase:
Study type: Observational

This study examines the extent of systemic muscle loss and the degree of fatigue experienced by breast cancer patients undergoing radiotherapy. This study seeks to identify whether muscle loss occurs outside the radiation fields and if muscle loss is correlated with the degree of fatigue.

NCT ID: NCT02565394 Completed - Fatigue Clinical Trials

Microbreaks in the OR to Mitigate High Physical and Mental Demands

OR-STRETCH
Start date: January 2, 2015
Phase: N/A
Study type: Interventional

Will targeted intraoperative exercises performed by surgeons during surgery, mitigate high physical and mental demands while enhancing performance during surgical procedures?

NCT ID: NCT02522988 Completed - Fatigue Clinical Trials

The Use of an Open Label Placebo to Treat Cancer Related Fatigue in Cancer Survivors

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

The purpose of this randomized-controlled, crossover pilot trial is to evaluate the feasibility, acceptability and effects of a non-deceptive (open-label) administration of placebo pills for treating cancer related fatigue (CRF). If significant effects are found, the investigators will later determine if the presence of a COMT Val18Met genotype variant predicts placebo responses.

NCT ID: NCT02521077 Withdrawn - Fatigue Clinical Trials

Intravenous Ascorbic Acid in Women Receiving Adjuvant or Neo-Adjuvant Chemotherapy for Early Stage Breast Cancer

Start date: May 2017
Phase: Phase 2
Study type: Interventional

This is a parallel-track, randomized study will observe whether intravenous ascorbic acid reduces the reported fatigue in women receiving adjuvant or neo-adjuvant chemotherapy for early stage breast cancer.

NCT ID: NCT02519205 Completed - Fatigue Clinical Trials

Measuring Fatigue in Triage: A Pilot Study

Start date: October 2015
Phase: N/A
Study type: Observational

The purpose of this study is to determine how the length of a triage shift (i.e. 4 vs., 8 vs., 12 hours) affects fatigue levels among triage nurses in the Emergency Department (ED).

NCT ID: NCT02518308 Completed - Depression Clinical Trials

Mindfulness Intervention in Reducing Anxiety in Patients Who Have Been Treated for Gynecologic Cancer

Start date: November 18, 2015
Phase: N/A
Study type: Interventional

This pilot clinical trial studies how well a mindfulness-based stress reduction (MBSR) intervention works in reducing anxiety in patients who have undergone treatment for gynecologic cancer but no longer have any sign of disease. Gynecologic cancer is cancer of the female reproductive tract, which includes the cervix, endometrium, fallopian tubes, ovaries, uterus, and vagina. Side effects from treatment for these cancers may include anxiety, fatigue, depression, and sexual function changes. Mindfulness training uses meditation and yoga to help patients focus on breathing, bodily sensations, and mental awareness. This may help decrease patients' stress and anxiety and improve their quality of life, and may also help their immune system.

NCT ID: NCT02517151 Recruiting - Clinical trials for Inflammatory Bowel Disease

Iron Supplementation in Inflammatory Bowel Disease (IBD) Patients With Chronic Fatigue

MICI_2011-01
Start date: October 2014
Phase: Phase 2
Study type: Interventional

A phase 2, randomized, placebo controlled trial evaluating the effects of n intravenous iron supplementation on chronic fatigue in IBD patients with controlled disease.

NCT ID: NCT02516189 Completed - Aging Clinical Trials

Strength Training for Elderlies and Their Effects on Muscle Fatigue and Microcirculation - Randomized Clinical Trial

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

The purpose of this study is to verify the effects of a strength training program on functional capacity, muscle performance and microcirculation in the elderly.

NCT ID: NCT02506504 Completed - Clinical trials for Obstructive Lung Diseases

Prevention of Post-exercise Muscle Fatigue and Effect on Exercise Training in Severe Patients With COPD.

QUADRIVEND
Start date: June 25, 2014
Phase: N/A
Study type: Interventional

In patients with severe Chronic Obstructive Pulmonary Disease (COPD), exercise tolerance is severely impaired due to a ventilatory limitation, levelling off the intensity of exercise. This reduces the physiological benefit of pulmonary rehabilitation. In these patients, it is then proposed to add an Inspiratory Pressure Support (IPS) in order to increase the intensity and the duration of every training session. In a preliminary study, the investigators showed that IPS applied during an exhaustive cycling exercise allowed to prevent the onset of post-exercise quadriceps fatigue evaluated by the endurance time to isotonic quadriceps contractions (TlimQ). The aim of this study is to determine the relationship between the prevention of post-exercise fatigue (TlimQ) and the change in training load (intensity x time x number of sessions) during a pulmonary rehabilitation programme. At the beginning of the training programme, 25 patients will be evaluated for TlimQ after a cycling exercise (70% maximal workload) with and without IPS in random order. The training load was then monitored at every exercise session of the programme.

NCT ID: NCT02506192 Completed - Chronic Pain Clinical Trials

Gulf War Illness Inflammation Reduction Trial

GWIIRT
Start date: July 2015
Phase: Phase 2
Study type: Interventional

The primary objective of this clinical trial is to determine if treatment with an anti-inflammatory drug (delayed-release prednisone) improves the health-related quality of life (HRQOL) of veterans with Gulf War Illness (GWI). The primary outcome measure is a change from baseline of HRQOL with respect to physical functioning and symptoms. Secondary outcomes measures include changes from baseline levels of GWI-associated biomarkers of inflammation in peripheral blood, GWI-associated symptoms (chronic pain, fatigue, and cognitive impairment), and HRQOL with respect to mental functioning.