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Fatigue clinical trials

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NCT ID: NCT04955587 Recruiting - Covid19 Clinical Trials

A Longitudinal Study on Longstanding Complicated Fatigue

Start date: August 24, 2021
Phase:
Study type: Observational [Patient Registry]

The purpose of the study is to investigate if there are common biopsychosocial vulnerability factors for developing and maintaining fatigue, regardless of the diagnosis. The investigators also believe that subgroups differ in terms of these factors. Participating patients with ME/CFS, burnout syndrome and post-covid fatigue complete a web form at inclusion and after 1, 2, 4, 6, 12, 18 and 24 months. There is no upper limit for the number of participants in the web survey. 150 participants are asked to submit blood samples at a local laboratory in connection with the questionnaires for analysis of inflammatory markers and one urine sample for analysis of nutritional markers. Two control groups are included, 150 patients with rheumatoid arthritis and 50 healthy individuals. The longitudinal design makes it possible to investigate how inflammatory markers, nutritional status, symptom burden, health related quality of life co-vary over time and how work ability and sick leave is affected.

NCT ID: NCT04943510 Recruiting - Exercise Clinical Trials

Characterization of Hamstring and Quadriceps Neuromuscular Fatigue After Soccer Game

QIF
Start date: November 4, 2021
Phase: Phase 2
Study type: Interventional

This is a monocentric study comparing hamstring and quadriceps neuromuscular fatigue after simulated soccer game, anaerobic and aerobic training sessions. The purpose of this study was: 1. To quantify the decrease of isometric force immediately after a simulate soccer game. 2. To characterize peripheral and central fatigue between hamstring and quadriceps muscles and described the kinetics of recovery after specific tasks of soccer training. 3. To compare the level neuromuscular fatigue induced by anaerobic and aerobic training. 4. To highlight correlation between neuromuscular fatigue and performance markers.

NCT ID: NCT04942444 Recruiting - Depression Clinical Trials

Effectiveness of Dry Needling in Fibromyalgia Patients

Start date: January 10, 2011
Phase: N/A
Study type: Interventional

Patients with fibromyalgia (FM) complain of widespread chronic pain from deep tissues including muscles. Previous research highlights the relevance of impulse input from deep tissues for clinical FM pain. Deep dry needle stimulation is an invasive treatment modality used in the management of musculoskeletal pain. Its efficacy has been confirmed in the management of myofascial trigger points, so the purpose of the study is to determine if blocking abnormal impulse input with deep dry needling stimulation of tender point may decrease hyperalgesia, clinical pain and associated symptoms such as anxiety, depression, fatigue and improve the quality of life in FM patients.

NCT ID: NCT04938362 Recruiting - Fatigue Clinical Trials

Cognitive Function and Fatigue After Brain Abscess

Start date: January 1, 2020
Phase:
Study type: Observational

Brain abscess is a focal bacterial or fungal infection of the brain. Treatment is neurosurgical drainage of pus followed by long-term antibiotic treatment. In spite of successful treatment of the infection, long-term cognitive problems or mental fatigue may ensue. The reason for this dysfunction may be a continuing inflammatory state or damage to brain tissue caused by the abscess. The investigators will evaluate these possibilities with the use of [18F]deoxyglucose-positron emission tomography (FDG-PET) and electroencephalography (EEG) in patients who have been treated for brain abscess and who experience cognitive problems and/or fatigue. FDG-PET may identify both inflammation and altered neuronal activity (the latter indicating damage to brain tissue), and EEG may identify altered neuronal activity, including changes in neuronal network activity.

NCT ID: NCT04921644 Recruiting - Clinical trials for Cancer-related Fatigue

Longitudinal Investigation of Cancer-related Fatigue and Its Treatment (LIFT Project)

Start date: August 20, 2021
Phase:
Study type: Observational

The LIFT project aims to thoroughly investigate the current status of health care in Germany regarding cancer-related fatigue from the institutional, professionals' and patients' perspective.

NCT ID: NCT04920045 Recruiting - Anemia Clinical Trials

A Trial to Assess the Effect of Transfusion Strategies on Fatigability Levels After Hospital Discharge

EToF
Start date: February 1, 2022
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial in which hospitalized patients with anemia are randomized to receive transfusion at: a) Hb<9g/dL (liberal transfusion strategy), or b) Hb<7g/dL (restrictive transfusion strategy). We are measuring self-reported fatigability, fatigue, and activity levels at randomization and 7 days post hospital discharge in both trial arms. In a subset of 75 patients in each trial arm (150 total), we will are administering the 6 Minute Walk Test at randomization and 7 days post discharge.

NCT ID: NCT04913558 Recruiting - Stress Clinical Trials

Effect of Aerobic Exercise on Stress and Fatigue of Lactating Employed Women

Start date: May 1, 2021
Phase: N/A
Study type: Interventional

The study aims to determine the effect of aerobic exercise on stress and fatigue of employed lactating women.

NCT ID: NCT04907513 Recruiting - Fatigue Clinical Trials

Amotivational Syndrome and Fatigue in Neurosurgery

DENI-CARE
Start date: December 4, 2021
Phase:
Study type: Observational

Depression is a major public concern associated with profound distress, intense suffering, and impairment in social, professional and familial functioning. Among the numerous symptoms defining depression, fatigue and motivation are not only frequent but also highly associated with poor quality of life and resistance to conventional antidepressant. Recent data, mainly obtained in animals, suggest that these symptoms may be linked to inflammatory processes within the central nervous system. Yet access to the brain is too invasive for exploring this link in patients with psychiatric conditions. However, certain conditions in neurosurgery, such as aneurysm rupture, require external evacuation, over several days or weeks, of the fluid bathing the brain through a catheter directly inserted into it. Critically, these patients also exhibit extreme exhaustion and fluctuating motivation, allowing to investigate the involvement of neuroinflammation in lack of motivation and fatigue by carrying out repeated motivation assessments with short behavioral tests (around ten minutes), while performing an analysis of inflammation markers in the fluid evacuated from the brain. The identification of inflammatory mechanisms underlying lack of motivation and fatigue could lead to the development of treatments for both resistant depression and motivation deficits that largely hamper rehabilitation in neurosurgery.

NCT ID: NCT04899635 Recruiting - Heart Failure Clinical Trials

POWER Myocardial Fatigue Study: a Biomechanical Assessment of Contractility of Human Myocardium

POWER
Start date: August 3, 2021
Phase:
Study type: Observational

To gain a comprehensive understanding of the biomechanical behaviour of human heart to explore the concept of myocardial fatigue in response to a temporal range of preload, afterload and drug-induced inotropy using in-vitro contractile assays.

NCT ID: NCT04893993 Recruiting - Clinical trials for Primary Biliary Cirrhosis

PBC Induced Fatigue Treated With Thiamine

PIFT
Start date: May 12, 2021
Phase: Phase 4
Study type: Interventional

Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease characterised by destruction of the intrahepatic bile ducts leading to liver inflammation and fibrosis, and ultimately liver cirrhosis and end-stage liver disease. More than 50% of patients with PBC suffer from chronic fatigue, and approximately 20% suffer from severe fatigue with negative impact on their quality of life. Although fatigue is a large problem in patients with PBC, no effective treatments are available. A Danish intervention study have shown that high dose oral thiamine (Vitamin B1) were effective in treating chronic fatigue in patients with inflammatory bowel disease. In this study, only few and minor adverse events to thiamine treatment were observed. Although the precise mechanism of work remains unknown, the investigators see no reason that this cannot be transferred topatients with PBC. Hence, the investigators aim to conduct a study investigating the use of oral thiamine in chronic fatigued patients with PBC. The study will be conducted as a double-blinded, placebo-controlled, randomised, crossover trial including 36 patients with PBC and with a higher fatigue level than in the general population for more than six months. The patients will be randomised into one of two 3x4 weeks setups; 1) thiamine for four weeks followed by four weeks washout and finally four weeks of placebo or 2) placebo for four weeks followed by four weeks washout and finally four weeks of thiamine. The primary endpoint is to investigate the fatigue-level before and after treatment with thiamine and placebo using every patient as their own control. Fatigue-level will be measured using international validated questionnaires. The doses of thiamine are calculated based on the patient gender and weight. All patients will be included in the outpatient clinic at the Department of Hepatology and Gastroenterology at Aarhus University Hospital.