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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06069635
Other study ID # RageH1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 17, 2022
Est. completion date July 17, 2023

Study information

Verified date October 2023
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical study is to investigate the effect of fatigue on balance, core endurance and player performance in adolescent football players. the main questions it aims to answer are: 1. What is the effect of fatigue on balance, core endurance and player performance in adolescent football players? 2. What is the effect of balance on player performance in adolescent football players? participants will be 60 male age from 16 to 18 years selected from Wadi-Degla football club randomly assigned into either fatigue or control group, Each player assessed for core endurance, balance and performance then fatigue protocol applied for the fatigue group and shame protocol for the control group and the repeat all measurements.


Description:

This study will be conducted in This pre and post controlled trial aiming at determining the efficacy of fatigue on core endurance, balance and player performance in adolescent football players, this study will be conducted in Wadi-Degla football club. Players will be randomly assigned into either fatigue or control group. Randomizations will be done using computer random generated numbers. Fatigue group (F.G): 30 players will be assessed for core endurance, balance and performance then fatigue protocol will be applied and reasses for core endurance, balance and performance after fatigue Control Group (C.G): 30 players will be assessed for core endurance, balance and performance. Players will be assessed at baseline and fatigue for: balance using (MFT challenge disc),Core endurance, 20-m running sprint and Triple-Hop Test (THT) for perfprmace Will apply RSA as fatigue protocol for the fatigue groupe. Inclusion criteria: Players will be included according to the eligibility Criteria


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 17, 2023
Est. primary completion date June 17, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 14 Years to 18 Years
Eligibility Inclusion Criteria: 1. age ranges from 14 to 18 years old 2. Players will selected from Wadi-Degla (2005, 2006 and 2007 football teams ) 3. All participants will be free from lower limb injuries for at least 6 months before the study 4. Body mass index will be at optimal (18.5 to 24.9) Exclusion Criteria: 1. Not regularly trained for at least 6 hours per week 2. Major lower limb injuries for at least 6 months before the study. 3. lower limb surgery for before the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Fatigue protocol (repeated sprint ability)
The test performed on an outdoor field (artificial grass carpet) in the form of 6 repetitions of maximal 2× 15 m shuttle sprints interspersed with 20 seconds of passive recovery , Before the RSA protocol, all players perform a brief standardized warm-up (approximately 20 minutes long), in 1at submaximal speed (followed by 40 seconds of passive recovery The fatigue index (FI) used to characterize the RSA performance was calculated in terms of percentage decrement score At the end of the RSA protocol , usually the time elapsed between the end of the last sprint and the beginning of the measurements was no more than 20 seconds, to avoid masking effects related to progressive recovery from fatigue.
Sham Comparator: Control group
approximately 20 minutes long), which consisted of : 6 minutes of incremental running from 60% to 80% of maximal aerobic speed; 6 minutes of dynamic flexibility exercises; 2 minutes of forward, backward, and lateral jogging and high-knee and ''butt-kick'' runs; 2 minutes of shuttle sprints (5 m in 1 direction and 5 m in the opposite direction, repeated for 2 minutes) at submaximal speed (followed by 40 seconds of passive recovery); and 2 minutes of RSA protocol simulation at submaximal speed (2 repetitions), again followed by 40 seconds of passive recovery. take apenalty of water and rest

Locations

Country Name City State
Egypt Cairo University Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary single-leg balance test The "MFT challenge disc" balance measuring system will be used to assess single-leg balance test (SLBT) for both the dominant (D) and non-dominant (N) legs (i.e., SLBT-D, SLBT-N). 20 seconds
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