Clinical Trials Logo

Fatigue clinical trials

View clinical trials related to Fatigue.

Filter by:

NCT ID: NCT04469010 Completed - Clinical trials for Cognitive Function and Mood

Efficacy Evaluation of 16 Weeks' Dietary Supplementation With Iron Bis-glycinate Plus Vitamin C on Cognitive Function, Subjective Mood, Fatigue, Health and Well-being

Start date: June 2, 2017
Phase: N/A
Study type: Interventional

Iron deficiency is the most prevalent nutritional deficiency worldwide with one in four estimated to be affected by iron deficiency anaemia. Women of reproductive age are at greatest risk for iron deficiency and anaemia due to iron losses during menstruation and childbirth as well as the increased need for iron throughout pregnancy. However, iron deficiency without anaemia is at least twice as common as iron deficiency anaemia with females aged 11-49 at the biggest risk of all. Despite this, it is commonly left undiagnosed. Those who are iron deficient non-anaemic can still suffer from the same common consequences of iron deficiency anaemia; these include unexplained fatigue, mood changes and decreased cognitive performance. However, randomised controlled trials (RCTs) assessing the effect of iron supplementation upon cognitive performance, mood, fatigue and well-being in non-anaemic iron deficient women of reproductive age are limited. There is also a lack of well-defined diagnostic criteria for non-anaemic iron deficiency, which makes comparisons across RCTs difficult. However, there is evidence to suggest that a haemoglobin cut off of ≥120 g/L and serum ferritin ≤ 20 µg/L provides an accurate indication of non-anaemic iron deficiency in women of reproductive age; this is inclusive of the ability to recognise iron-associated deficits in psychological and physiological functioning. Additionally, previous RCTs could be improved by utilising a lower dose of iron in a bis-glycinate chelate form, which is evidenced to have superior bioavailability, tolerability and subsequent efficacy compared to ferrous formulations. Iron bis-glycinate absorption is also negatively associated to serum ferritin levels, which is suggestive of a non-anaemic iron deficient population benefitting most from it's administration. The current study aims to build upon previous iron RCTs in populations of non-anaemic iron deficient and iron sufficient women of reproductive age by investigating the effects of 16-weeks supplementation with either iron bis-glycinate chelate alone, iron bis-glycinate plus vitamin C (as ascorbic acid) or matched placebo upon cognitive performance, subjective mood, fatigue, health and well-being.

NCT ID: NCT04468191 Withdrawn - Clinical trials for Amyotrophic Lateral Sclerosis

Fatigue in Patients With Amyotrophic Lateral Sclerosis

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Expiratory muscle strength training (EMST) is an emerging palliative intervention for prolonging pulmonary and swallow function in patients with amyotrophic lateral sclerosis (PALS), but it is unknown whether EMST may result in detrimental immediate to short-term fatigue because there is no way to measure fatigue non-invasively. This study will determine the immediate to short-term impact of EMST on objective respiratory and swallow function, whether subjective ratings of dyspnea and fatigue map to objective decompensation of respiratory and swallow function, and the ability to monitor fatigue of the respiratory and swallowing musculature non-invasively. Findings from this research study will provide preliminary evidence regarding optimal timing for PALS to complete EMST and will provide PALS and clinicians increased capabilities to monitor fatigue non-invasively.

NCT ID: NCT04467749 Completed - Clinical trials for Spinal Cord Injuries

Effects of In-Wheel Suspension

Start date: July 14, 2022
Phase: N/A
Study type: Interventional

Manual wheelchairs allow individuals with spinal cord injuries (SCI) to safely and effectively access their environment. However, continual exposure to whole body vibration (WBV) is one of many contributing factors to neck pain, back pain, and fatigue in wheelchair users with SCI. Vibration-reducing in-wheel suspension has the potential to mitigate issues associated with long-term manual wheelchair propulsion. Evidence is lacking on how well these systems work for reducing harmful shock and vibration, pain and fatigue. The purpose of this study is to examine how these wheels change the vibration levels manual wheelchair users are exposed to and how they impact pain and fatigue.

NCT ID: NCT04467645 Completed - Healthy Clinical Trials

The Effect of Reflexology on Sleep Quality and Fatigue in Postmenopausal Women

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Introduction: This study was conducted to determine the effect of reflexology on sleep quality and fatigue in postmenopausal women.

NCT ID: NCT04467255 Recruiting - Diabetes Mellitus Clinical Trials

Surface Electromyography Study of Fatigue in Diabetic Neuropathy

Start date: May 3, 2018
Phase: N/A
Study type: Interventional

Fatigue in diabetic neuropathy compromises patients' physical activity and poses questions on how to plan correct rehabilitation training. Conclusive interpretation of muscular mechanisms of fatigue in diabetic neuropathy has not yet been achieved. Among the various instrumental evaluations for fatigue, multichannel surface electromyography (sEMG) is a recognized tool that permits the study of myoelectric manifestations of fatigue. Aim of the study is to assess if differences in myoelectric manifestations of fatigue between patients affected by diabetic neuropathy exist after an aerobic or endurance training.

NCT ID: NCT04456764 Active, not recruiting - Fatigue Clinical Trials

The Sleep and Teamwork in EMS Study

SaFTiE
Start date: September 16, 2020
Phase: N/A
Study type: Interventional

More than half of Emergency Medical Services (EMS) workers report work-related mental and physical fatigue. Odds of injury among fatigued EMS workers are nearly double that of non-fatigued workers. There is a compelling need to reduce fatigue among EMS workers, yet few EMS organizations have a formal fatigue management program and many may not be cost-effective or evidence-based. This trial addresses national goals of the National Occupational Research Agenda (NORA) and tests a novel approach to fatigue risk management that is easily scalable to large workforces and low-cost for employers of shift workers.

NCT ID: NCT04455009 Completed - Fatigue Clinical Trials

Acute Effects of Fitness Drink Formulas on Energy Expenditure and Fat Metabolism

Start date: March 8, 2018
Phase: N/A
Study type: Interventional

The purpose of this investigation was to examine the acute effects of consuming two different fitness drink formulas on the physiological response at rest and to exercise in healthy men and women.

NCT ID: NCT04448977 Recruiting - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

Examining Effects of Ocrevus on Cognitive Fatigue Using fMRI

Start date: May 6, 2021
Phase:
Study type: Observational

The purpose of this research study is to investigate the effectiveness of MS Disease modifying medications on cognitive fatigue in persons with relapsing remitting multiple sclerosis (RRMS). Cognitive fatigue is the kind of fatigue that occurs after intense mental concentration as after a session of problem solving.

NCT ID: NCT04448925 Completed - Clinical trials for Exercise, Cardiovascular Function, Fatigue, Muscular Power

Physiological Responses to Maximal 4-s Sprint Interval Cycling

Start date: January 10, 2019
Phase: N/A
Study type: Interventional

The optimal recovery duration depends on the intensity of exercise and in the present study the intensity was maximal power for 4-s while cycling an 'Inertial Load' ergometer (ILE). Recovery duration of 15, 30 and 45-s were given between 30 successive sprints.

NCT ID: NCT04441840 Completed - Muscle Damage Clinical Trials

Immune and Recovery Modulating Impact of Probiotic Supplementation After Intense Resistance Exercise

Start date: April 16, 2019
Phase: N/A
Study type: Interventional

This study proposal seeks to examine the efficacy of probiotic supplementation at mitigating changes in immune function and recovery after completion of intense, stressful exercise while also allowing for a better understanding of its ability to promote recovery and maintenance of physical performance.