Clinical Trials Logo

Fatigue, Mental clinical trials

View clinical trials related to Fatigue, Mental.

Filter by:
  • None
  • Page 1

NCT ID: NCT06281795 Not yet recruiting - Efficacy, Self Clinical Trials

Neuromodulation of the Autonomic Nervous System in Athletes

NANSA
Start date: April 1, 2024
Phase: N/A
Study type: Interventional

There are few studies in the literature that have evaluated the effects of using percutaneous stimulation of the auricular branch of the vagus nerve for sports purposes (to accelerate recovery after physical exertion). It has been demonstrated that tVNS in athletes improved the rate of heart rate recovery, reduced lactic acid levels in blood plasma, reduced pain, reduced overtraining syndrome and fatigue levels.

NCT ID: NCT06042530 Recruiting - Clinical trials for Cognitive Impairment

Cognitive Impairment and Fatigue After Mild to Moderate COVID-19

Start date: April 1, 2021
Phase:
Study type: Observational

The primary aim of the project is to map fatigue, cognitive and visual dysfunctions and possible underlying pathophysiological mechanisms in persons with long-term symptoms after a mild to moderate COVID-19 infection. Secondary goals are to study whether covarying factors such as depression and sleep disorders contribute to the results.

NCT ID: NCT05116332 Completed - Surgery Clinical Trials

Comparing the Variation in Laparoscopic Skills Acquisition in Obstetrics & Gynaecology and General Surgical Trainees

LAGGS
Start date: September 11, 2021
Phase:
Study type: Observational

The investigators postulate that there is a difference in the acquisition of Fundamental Laparoscopic Skills (FLS) between general surgical and Obstetrics & Gynaecology (O&G) trainees. This discrepancy is also likely to influence the musculoskeletal and cognitive fatigue trainees experience within both specialties. Additionally there is likely to be a discrepancy in the expectations of consultants and trainees on skills perceived to be important at the completion of training (CCT). This study aims to compare and evaluate the discrepancy in FLS acquisition amongst O&G and GS trainees in order to identify areas for improvements in the training pathway, the associated fatigue experience and highlight the expectations perceived to be required at the completion of training.

NCT ID: NCT04974606 Completed - Mood Clinical Trials

Effect of Coffeeberry on Mood, Motivation and Cognitive Performance

Start date: June 28, 2016
Phase: N/A
Study type: Interventional

The primary purpose is to test the short-term effects of the acute consumption of two novel beverages made from coffeeberries, the fruit of the coffee plant (Coffea arabica) benchmarked against caffeine on several aspects of cognitive performance. Preliminary studies suggest that flavanols and chlorogenic acids can enhance cognitive performance. It is unknown if drinks formulated with flavanols and chlorogenic acids (without high sugar or caffeine) improve cognition or mood to a similar extent as caffeine. Coffeeberry beverage comparisons will be made to a flavored positive control beverage containing caffeine and a flavored placebo beverage.

NCT ID: NCT04476615 Completed - Diet, Healthy Clinical Trials

Effects of Fasting-Mimicking Diet on Central and Peripheral Components of Fatigue, Muscular Resistance

FMD_Exercise
Start date: December 4, 2017
Phase: N/A
Study type: Interventional

The aim of the study is to test a Fasting Mimicking Diet (FMD) for its efficacy on improving muscular resistance and endurance. The investigators will perform a randomized clinical trial to test the efficacy of the FMD on improving muscular strength, muscular resistance and endurance in physically active young adults (18-40 years of age). The study will include two arms: Placebo (Placebo diet) and FMD (3 cycles of 5-day fasting-mimicking diet within two months). Study endpoints will include muscular strength evaluation of lower limbs, cardio-pulmonary responses, neuromuscular function and muscle architecture. Subjects will be evaluated 4 times within 3 months: at baseline (T1), after the 1st cycle of diet (T2), 7 to 15 days after the 3rd cycle of diet maintaining baseline intensity (T3) and with re-assessment of Peak Power Output (T4).