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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04748497
Other study ID # APHP201139
Secondary ID 2020-A02919-30
Status Recruiting
Phase N/A
First received
Last updated
Start date January 8, 2021
Est. completion date June 2024

Study information

Verified date March 2022
Source Assistance Publique - Hôpitaux de Paris
Contact Jean François Toussaint, MD, PhD
Phone +33 (0)1 42 34 82 10
Email jean-francois.toussaint@aphp.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of the study: improvement of sportive performances by quantification and performances monitoring of paralympic athletes. The secondary objectives of the study: - quantification and performances monitoring of mechanical performances during the filed tests, the laboratory analysis and the sportive competitions; - quantification and performances monitoring of physiological performances during the filed tests, the laboratory analysis and the sportive competitions; - quantification and risk monitoring of discipline-relative musculo-squeletic troubles, caused by training or using of sportive equipment; - quantification and mechanical monitoring by the made-to-measure or usual sportive material.


Description:

The sportive performance results from a range of determinations such as: physiological, biomechanical, morphological, psychological, social and environmental factors. The interactions between athletes, equipment, training and environment influences the development of athletes' performance. In the context of the coming Paris 2024 Paralympic Games, the performance construction for the exploration, the quantification and the management of all factors is an commun objective between sportive team, medical team and researchers.


Recruitment information / eligibility

Status Recruiting
Enrollment 134
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria: - High-lever paralympic athletes registered on the ministerial list or selected by Parasport Federation of France or Shooting Federation of France; - Aged >= 14 years; - Informed consent signed by adult athlete or by holder of parental authority or guardian for minor athlete; - Covered by social security system. Exclusion Criteria: - Temporary or definitive contraindication to the practice of the affected sport activity; - Undergoing anti-coagulated treatments; - Cognitive disabilities conducting impossibility to participating to clinical trial, such as serious cognitive troubles, behaviors troubles, psychic troubles or upgraded curatorship needing; - Under guardianship or judicial decision; - Ongoing pregnancy.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Standardization of evaluation and follow-up
Standardization of evaluation and clinical and sportive follow-up of athletes. Made-to-measure technical supports will be tested regarding the Paralympic regulations.

Locations

Country Name City State
France Service Médecine Physique et de Réadaptation, Hôpital Raymond Poincaré, APHP Garches

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dynamic sportive activity Dynamic sportive activity: Sprint Capacity Test will be used to have maximal speed. through study completion, an average of 1 year
Primary Dynamic sportive activity Dynamic sportive activity: Sprint Capacity Test will be used to have maximal speed. at 42 months
Primary Static sportive activity Static sportive activity: maximal speed of movement of pression center. through study completion, an average of 1 year
Primary Static sportive activity Static sportive activity: maximal speed of movement of pression center. at 42 months
Secondary Biomechanical indices of performance: isometric power measurement Isometric power will be measured by MicroFet & handgrip of 26 measures, advice for healthcare professionals to measure handgrip strength forces to test and document grip deficits and to evaluate consistency of effort. through study completion, an average of 1 year
Secondary Biomechanical indices of performance: arms and shoulder's Strength Arms and shoulder's Strength will be measured by force platform. through study completion, an average of 1 year
Secondary Physiological indices of performance: maximal aerobic speed (MAS) Maximal aerobic speed (MAS) will be measured by Repetition Per Minute on a Arm ergometer. Twice through study completion, an average of 42 months
Secondary Physiological indices of performance: maximal aerobic power Maximal aerobic power will be measured by following Watts fluctuation during the incremental hand-biking test. Twice through study completion, an average of 42 months
Secondary Fatigue assessment Fatigue assessment will be measured by Fatigue Index (Power max ratio). Twice through study completion, an average of 42 months
Secondary Blood lactate concentration Blood lactatemia level will be measured by lactometer. immediately after the intervention
Secondary VO2 peak oxygen uptake VO2 peak oxygen uptake through study completion, an average of 1 year
Secondary Peak breath expiration volume assessment VE peak: peak breath expiration volume through study completion, an average of 1 year
Secondary Peak cardiac frequence CF: peak cardiac frequence through study completion, an average of 1 year
Secondary Musculo-squeletic troubles risks measurement Musculo-squeletic troubles risks will be measured by medical following and clinical method of functional assessment of the shoulder (i.e. "Constant scale"). through study completion, an average of 1 year
Secondary Time and distance of deceleration of wheelchair during riding test Time and distance of deceleration of wheelchair during riding test: measured by signal analysis of instrumented wheelchair (inertial control units). through study completion, an average of 1 year
Secondary Mechanical indices of wheelchair propulsion - applied forces on handrim during the propulsion Applied forces on handrim during the propulsion: measured by force platform. through study completion, an average of 1 year
Secondary Acceleration profil during the propulsion through study completion, an average of 1 year
Secondary Speed profil during the propulsion through study completion, an average of 1 year
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