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Fatigue clinical trials

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NCT ID: NCT02924831 Not yet recruiting - Clinical trials for Chronic Fatigue Syndrome

High-tech Acupuncture for Treatment of Chronic Fatigue Syndrome

Start date: November 2016
Phase: Phase 2
Study type: Interventional

1. To study the relationship between Chronic Fatigue Syndrome (CFS) and heart rate (HR) and its variability (HRV). 2. To compare the curative effects and the HR/HRV indices between applicationa of different acupoints as well as different treatments (acupuncture and moxibustion).

NCT ID: NCT02923102 Completed - Healthy Volunteers Clinical Trials

Effects of Recoverben® on Recovery After Exhaustive Exercise

Start date: October 2016
Phase: N/A
Study type: Interventional

The aim of the study is to investigate a pre and post workout supplementation (15 days) with Recoverben® , a Aloysia citriodora extract on recovery after exhaustive exercise. Effects will be investigated with 400mg Recoverben® and compared to placebo.

NCT ID: NCT02922439 Completed - Depression Clinical Trials

Health Literacy Assessment and Intervention to Reduce Disparities: FLIGHT/VIDAS II

FV2
Start date: August 21, 2018
Phase: N/A
Study type: Interventional

The purpose of this study will to be to evaluate the effects of a mobile intervention focused on improving the chronic disease self management skills of individuals with low health literacy. The intervention will provide information that culturally and linguistically tailored to participants' level of health literacy.

NCT ID: NCT02916355 Completed - Adiposity Clinical Trials

Role of Interleukin (IL)-1 in Postprandial Fatigue - The Chäschüechli 2 Study

Chäs2
Start date: August 2016
Phase: N/A
Study type: Interventional

Role of IL-1 in postprandial fatigue - The Chäschüechli 2 Study It is a randomized, single dose, placebo-controlled, double blind, cross-over, proof-of-concept study. 16 healthy young men will be included in this study. The objective of this study is to evaluate if severity of postprandial fatigue is driven by IL-1. Since fatigue is associated with increased cytokine levels, and since fatigue in chronic inflammatory settings, such as type 2 diabetes, can be reduced by inhibition of IL-1β, postprandial fatigue might also respond to anti-inflammatory intervention with IL-1 inhibition. The aim of the study is to investigate whether postprandial fatigue is, at least in part, driven by the IL-1 system.

NCT ID: NCT02914964 Active, not recruiting - Multiple Sclerosis Clinical Trials

Dietary Approaches to Treat Multiple Sclerosis-Related Fatigue Study

Waves
Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect of the Swank Diet (low saturated fat) and the Wahls Elimination Diet (modified paleo) on fatigue levels in individuals with relapsing-remitting multiple sclerosis who have documented fatigue. Participants will follow their usual diet for 12 weeks and then be randomly assigned to follow one of the two diets for 24 weeks.

NCT ID: NCT02913209 Active, not recruiting - Multiple Sclerosis Clinical Trials

Quantitative Fatigue and Muscle Performance in Multiple Sclerosis

Start date: April 2016
Phase:
Study type: Observational

Fatigue is consistently rated as the top symptomatic complaint for individuals with multiple sclerosis (MS). Currently, the MS Fatigue Impact Scale (MFIS), a subsection of the Multiple Sclerosis Quality of Life (MSQoL), is the clinical standard used by neurologists for monitoring and tracking fatigue in individuals with MS. However, fatigue is multidimensional phenomenon and subjective measures have had poor or limited relationships with functional status. While previous study has focused on contributing factors to fatigue such as sleep disorders and diminished cortical excitability, this line of inquiry has neglected the role of muscle structure and function on fatigue in every day functional tasks. An alternative approach is to assess quantitative fatigue using anaerobic testing methods. However, more knowledge is needed to understand the role that quantitative fatigue plays in self-reported fatigue measures and function of daily activities. Our purpose is to determine the association between quantitative fatigue tests with performance-based measures of mobility and self-reported health-related quality of life. Our secondary goal is to understand how the intrinsic properties of muscle tissue influence muscle performance in Veterans with MS.

NCT ID: NCT02911649 Completed - Breast Cancer Clinical Trials

Reducing Sedentary Behaviour With Technology

Start date: September 2016
Phase: N/A
Study type: Interventional

Cancer-related fatigue (CRF) can be experienced by individuals with Prostate Cancer (PC), which can have profound effects on their well-being. Although physical activity has been shown to improve CRF, the recommended levels are generally not met. Step count and distance traveled information can help individuals to increase their physical activity. Wearable technology (WEAR) provides the user with feedback of their physical activity which can motivate behaviour change. Similarly, education workshops (EDU) on the effects of sedentary behaviour and physical activity may also reduce sedentary behaviour. The objectives of this study are to evaluate the effects of WEAR and EDU on sedentary behaviour and CRF, and to explore the feasibility of WEAR in this population. Participants in this study will be randomly assigned into WEAR, EDU, WEAR+EDU, or control over a three-month intervention. Assessments at baseline, post-intervention and a 3-month follow up will evaluate CRF, quality of life and level of sedentary behaviour, and use of WEAR devices. The results from this study will provide evidence-based knowledge on the impact of WEAR and EDU on sedentary behaviour and CRF, and an understanding on the use of technology within the PC population. These results can shape the development of programming for CRF and the use of scale-able technology-based interventions/approaches in this population.

NCT ID: NCT02895997 Completed - Mental Fatigue Clinical Trials

Turning Night Into Day: Transcontinental Provision of Telehealth By and For the Emory Community

Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if temporarily relocating clinicians who deliver remote care using the eICU telehealth system to Sydney, Australia will lead to greater job satisfaction, reduced physiologic stress, and improve performance. Four nurses and six physicians will be sent to a site in Sydney Australia on a rotating basis to determine whether providing care during the Australian daytime is more efficient and precise than providing care during the night in the United States.

NCT ID: NCT02890316 Completed - Breast Cancer Clinical Trials

Assessment of Fatigue During Radiotherapy for Breast Cancer With and Without Homeopathy Treatment

Start date: July 2016
Phase: N/A
Study type: Interventional

To evaluate the effects of homeopathy treatment on radiotherapy-induced fatigue, cognitive and emotional functions.

NCT ID: NCT02885285 Terminated - Parkinson's Disease Clinical Trials

The Impact of Three Distinct Exercise Types on Fatigue, Anxiety, and Depression in Parkinson's Disease

PD&Exercise
Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to learn about the impact of exercise on fatigue, anxiety, and depression in Parkinson's disease. It is well established that exercise improves the motor symptoms of Parkinson's disease. However, it is not clear which types of exercise are most beneficial for specific non-motor symptoms.