- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07329348
Comparison of Accentuated Eccentric and Concentric Resistance Training in Athletes.
Comparison of Accentuated Eccentric and Concentric Resistance Training on Aerobic Capacity and Strength in Athletes.
Study Overview
Status
Conditions
Detailed Description
Study Design: Randomized Clinical Trials Sample size: 78(39 for each group) Sampling technique: Non-probability, Purposive sampling technique
Study Setting:
- Pakistan Football Federation, Lahore
- Model town soccer club, Lahore
Inclusion criteria:
- Male soccer players
- Age 18 to 30 years.
- A minimum of two years of experience in Regular training
- Athletes with BMI 18.5kg/m2 -24.9kg/m2
Exclusion criteria:
- History of lower extremity surgeries (e.g., ACL reconstruction or any major surgery) in the past year
- Athletes having consumption of Drugs which may influence Athlete performance.
- Any systemic illness
- Any musculoskeletal disorder
- Pre-existing Cardiovascular and respiratory (exercise-induced asthma) conditions
Tools:
- Aerobic capacity:20-meter shuttle run test (ICC =0.96)
- Muscle strength :1RM Back squat test (ICC=0.91-0.99)
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Model Town Football Club
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Male soccer players
- Age 18 to 30 years.
- A minimum of two years of experience in Regular training
- Athletes with BMI 18.5kg/m2 -24.9kg/m2
Exclusion Criteria:
• History of lower extremity surgeries (e.g., ACL reconstruction or any major surgery) in the past year
- Athletes having consumption of Drugs which may influence Athlete performance.
- Any systemic illness
- Any musculoskeletal disorder
- Pre-existing Cardiovascular and respiratory (exercise-induced asthma) conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A
The AERT group performed eccentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks.
Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set.
Participants in this group start with Yellow band (light resistance) and progressing through to purple band (high resistance).
The level of exercise progressively increased throughout the 8-week program, by increasing the resistance of resistance bands.
In group A, participants executed the Eccentric Phase for 2-4 seconds and Concentric phase for 1-2 seconds.
|
The AERT group performed eccentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks.
Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set.
Participants in this group start with Yellow band (light resistance) and progressing through to purple band (heavy resistance).
The level of exercise progressively increased throughout the 8-week program, by increasing the strength of resistance bands.
In group A, participants executed the Eccentric Phase for 2-4 seconds and Concentric phase for 1-2 seconds.
12 Comparison of accentuated eccentric and concentric resistance training in athletes
|
|
Experimental: Group B
The CRT group performed concentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks.
Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set.
Participants in this group start with Yellow band (light resistance) and progressing through to purple band (high resistance).
The level of exercise progressively increased throughout the 8-week program, by increasing the resistance of resistance bands.
In group B, participants executed the Concentric Phase for 2-4 seconds and Eccentric phase for 1-2 seconds.
|
The CRT group performed concentric resistance training by Elastic Resistance bands for 3 sessions per week for 8 weeks.
Each session included 3 sets of 10 repetitions with 2-3 mints of rest interval between each set.
Participants in this group start with Yellow band (light resistance) and progressing through to purple band (heavy resistance).
The level of exercise progressively increased throughout the 8-week program, by increasing the strength of resistance bands.
In group B, participants executed the Concentric Phase for 2 4 seconds and Eccentric phase for 1-2 seconds.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
1-RM Back Squat test
Time Frame: 8 weeks
|
a warm up of 10 repetitions using an empty barbell in back squat position. After rest of 2 mints, Participants will perform same protocol with addition of (35 pounds) weight and goal is to perform maximum repetitions. At final phase, weight (35 pounds) and the maximum repetitions performed are counted. This count is then used in Epley formula to calculate the individual 1RM (32). Epley's Formula: 1RM = weight x (1 + (reps / 30)) |
8 weeks
|
|
20-MTR Shuttle Run test
Time Frame: 8 weeks
|
The 20-meter shuttle run test, often called the "beep" or "bleep" test, requires participants to run back and forth continuously between two lines 20 meters apart, with a rhythm imposed by audio(beep).
Starting at a slow pace, they must turn when signaled by the beeps.
After about a minute, the pace increased, with the beeps occurring more quickly, requiring the runners to speed up.
The speed increases each minute(level), with beeps becoming closer together.
If a participant reaches the line before the beep, they must wait; if not, they receive a warning and have two more chances to catch up to the pace.
A second warning results in elimination from the test.
Calculation: VO2max = 18.043461 + (0.3689295 x TS) + (- 0.000349 x TS x TS)
|
8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: ayesha aslam, DPT, Riphah International University
- Principal Investigator: Muhammad faheem Afzal, MS-SPT, Riphah International University
Publications and helpful links
General Publications
- Tayfur B, Charuphongsa C, Morrissey D, Miller SC. Neuromuscular Function of the Knee Joint Following Knee Injuries: Does It Ever Get Back to Normal? A Systematic Review with Meta-Analyses. Sports Med. 2021 Feb;51(2):321-338. doi: 10.1007/s40279-020-01386-6.
- Teoldo I, Dambroz F, Brito J. Performance of soccer players under acute physical fatigue: An approach based on cognitive, tactical and physical aspects. Heliyon. 2024 Apr 30;10(9):e30516. doi: 10.1016/j.heliyon.2024.e30516. eCollection 2024 May 15.
- Businari GB, de Camargo JBB, Barbosa PH, Brigatto FA, Aoki MS, Braz TV, Lopes CR. Chronic Effects of Heavy Load Activity Performed Before Resistance Training Sessions on the Physical Performance of Youth Soccer Players. Int J Exerc Sci. 2022 Feb 1;14(6):1421-1434. doi: 10.70252/SDEL8387. eCollection 2021.
- Leao C, Silva AF, Badicu G, Clemente FM, Carvutto R, Greco G, Cataldi S, Fischetti F. Body Composition Interactions with Physical Fitness: A Cross-Sectional Study in Youth Soccer Players. Int J Environ Res Public Health. 2022 Mar 18;19(6):3598. doi: 10.3390/ijerph19063598.
- Almaawi A, Awwad W, Bamugaddam A, Alasheikh M, Muaddi M, Almutair O, Alomar AZ. Prevalence of knee injuries among male college students in Riyadh, Kingdom of Saudi Arabia. J Orthop Surg Res. 2020 Mar 31;15(1):126. doi: 10.1186/s13018-020-01638-1.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- REC/RCR&AHS/24/0481
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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