Overtraining Syndrome Clinical Trial
— SuPpOrtOfficial title:
The Evaluation of Cell-Free Plasma DNA (cfDNA) and Oxidative Stress Indices as Biomarkers for the Diagnosis and Prevention of Overtraining
NCT number | NCT03833973 |
Other study ID # | SuPpOrt-UTH |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 1, 2018 |
Est. completion date | July 30, 2020 |
Athletic training aims to increase and improve physical performance that is achieved through training overload combined with periods of rest and recovery. Overtraining syndrome (OTS) is associated with an imbalance between training and recovery. The symptoms associated with OTS vary between individuals and may reflect parasympathetic and/or sympathetic nervous system alterations as well as endocrine irregularities. The prevalence is not known, but it is usually reported among endurance athletes, such as cyclists, distance runners and triathletes. It appears that OTS represents a systemic inflammatory process with diffuse effects on the neurohormonal axis affecting host immunology and mood. Previous works, showed that cell-free DNA (cf-DNA) is correlated with the severity of excessive exercise-induced inflammation as well as with trauma and stroke severity suggesting that it might be used as a potential clinical marker for athletes with overtraining syndrome. Oxidative stress indices can be determined non-invasively and may reflect inflammatory responses after training suggesting that they could be used as clinical markers for the diagnosis of OTS. However, there are no available biomarkers to aid towards the diagnosis and/or prevention of OTS, except that of the persistence of unexplained underperformance despite an extensive recovery of the athlete. Therefore, the purpose of this study is to evaluate the potential of cf-DNA and selected oxidative stress variables as diagnostic biomarkers of OTS.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | July 30, 2020 |
Est. primary completion date | June 1, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 15 Years to 40 Years |
Eligibility |
Inclusion Criteria for Runners: Participants: - should be long-distance runners, marathon runners, 5 km and 10 km runners. - should be able to provide the daily training plan and a 7-day dietary recall every month. - should be considered elite level runners. - should be free of musculoskeletal injuries for at least one year before the study. Inclusion Criteria for Soccer Players: Participants: - should be elite soccer players. - should be able to provide the daily training plan and a 7-day dietary recall. - should be participated in matches. - should be free of musculoskeletal injuries for at least one year before the study. Exclusion Criteria (both Runners and Soccer Players): If participants: - do not adhere to rules of the study. - have a recent history of illness or injury . - do not participate in competitive training. |
Country | Name | City | State |
---|---|---|---|
Greece | Exercise Biochemistry Laboratory, School of Physical Education & Sports Sciences, University of Thessaly | Tríkala |
Lead Sponsor | Collaborator |
---|---|
University of Thessaly |
Greece,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in cell free plasma DNA | Cell free plasma DNA will be measured with real-time PCR in plasma samples. | At baseline, at six months and at twelve months | |
Primary | Change in Cortisol level | Cortisol concentration will measured in serum | At baseline, at six months and at twelve months | |
Primary | Change in Testosterone level | Testosterone concentration will be measured in serum | At baseline, at six months and at twelve months | |
Primary | Change in cytokine response | Concentration of TNF-a, IL-6 and IL-10 will be measured in plasma. | At baseline, at six months and at twelve months | |
Primary | Change in creatine kinase in plasma | Concentration of creatine kinase will be measured in plasma | At baseline, at six months and at twelve months | |
Primary | Change in uric acid in plasma | Concentration of uric acid will be measured in plasma | At baseline, at six months and at twelve months | |
Primary | Change in protein carbonyls in blood | Concentration of protein carbonyls will be measured in red blood cells | At baseline, at six months and at twelve months | |
Primary | Change in total antioxidant capacity | Total antioxidant capacity will be measured in plasma | At baseline, at six months and at twelve months | |
Primary | Change in reduced glutathione in blood | Concentration of reduced glutathione will be measured in in red blood cells | At baseline, at six months and at twelve months | |
Primary | Change in oxidized glutathione in blood | Concentration of oxidized glutathione will be measured in red blood cells | At baseline, at six months and at twelve months | |
Primary | Change in catalase activity | Catalase activity will be measured in red blood cells | At baseline, at six months and at twelve months | |
Primary | Change in malondialdehyde in blood | Concentration of malondialdehyde will be measured in serum | At baseline, at six months and at twelve months | |
Secondary | Change in blood lactate concentration | Blood lactate concentration will be measured during a maximal lactate steady-state test. | At baseline, at six months and at twelve months | |
Secondary | Change in peak torque | Peak torque will be assessed on an isokinetic dynamometer at 60 degrees/sec | At baseline, at six months and at twelve months | |
Secondary | Change in orthostatic heart rate. | Heart rate will be measured in a resting position and following 15 seconds of standing by heart rate monitor. | At baseline, at six months and at twelve months | |
Secondary | Change in jumping ability. | Jumping ability will be assessed by measuring squat jump. | At baseline, at six months and at twelve months | |
Secondary | Change in flexibility | Flexibility will be assessed through the sit and reach test. | At baseline, at six months and at twelve months | |
Secondary | Change in body composition. | Body composition will be assessed by dual energy X-ray absorptiometry (DXA) | At baseline, at six months and at twelve months | |
Secondary | Change in delay onset of muscle soreness (DOMS) | DOMS will be assessed by muscle palpation while participants are laying , standing and after performing 3 squats. | At baseline, at six months and at twelve months | |
Secondary | Change in complete blood count | Complete blood count analysis will be performed on an automatic blood analyzer. | At baseline, at six months and at twelve months | |
Secondary | Change in RSA | 5 x 30 m sprints will be performed with 25 seconds rest in-between. Mean time for 5 sprints and fatigue index will be calculated. | At baseline, at six months and at twelve months | |
Secondary | Change in Yo-Yo IE2 | Yo-Yo IE2 will be assessed using a standardized testing protocol. | At baseline, at six months and at twelve months | |
Secondary | Change in Yo-Yo IR2 | Yo-Yo IR2 will be assessed using a standardized testing protocol. | At baseline, at six months and at twelve months | |
Secondary | Change in Spreed | Spreed will be assessed using a standardized testing protocol in 10 and 30 meters. | At baseline, at six months and at twelve months | |
Secondary | Dietary intake | Dietary intake will be assessed using 7-day diet recalls. | At baseline, at six months and at twelve months | |
Secondary | Change in jumping ability. | Jumping ability will be assessed by measuring counter-movement jump. | At baseline, at six months and at twelve months | |
Secondary | Change in jumping ability. | Jumping ability will be assessed by measuring drop jump. | At baseline, at six months and at twelve months |
Status | Clinical Trial | Phase | |
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Recruiting |
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