EFFECT OF ECCENTRIC AND CONCENTRIC EXERCISE PROGRAMS For HAMSTRING GRADE INJURIES
Eccentric vs. Concentric Training: Accelerating Recovery in Elite Athletes With Grade II Hamstring Injury
1 other identifier
interventional
30
1 country
1
Brief Summary
Hamstring injuries are common and recurrent in both elite and recreational athletes, often leading to prolonged absence from sports. The aim of this study is to compare the effects of eccentric and concentric exercise programs on the recovery of elite athletes diagnosed with grade II hamstring strain. Pain, flexibility, muscle strength, balance, and return-to-sport duration will be evaluated to determine the impact of different exercise modalities. Dynamic balance assessment will also be performed before and after treatment. The two intervention groups will be compared using the Wilcoxon test, with p\<0.01 considered statistically significant. This study is expected to provide evidence on which exercise program is more effective in facilitating return to sport and to contribute to improved rehabilitation strategies in future athletic injuries.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2018
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 20, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 17, 2024
CompletedFirst Submitted
Initial submission to the registry
August 20, 2025
CompletedFirst Posted
Study publicly available on registry
August 27, 2025
CompletedAugust 27, 2025
August 1, 2025
5.9 years
August 20, 2025
August 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time to Return to Sport
he duration (in days) from the start of the rehabilitation program until the athlete meets all return-to-play criteria, including complete pain relief, sufficient muscle strength, joint mobility, flexibility, running and gait analysis, physical fitness, balance, dynamic functional performance, lumbopelvic motor control, and subjective readiness reported by the athlete.
From baseline until return to sport, up to 12 weeks
Study Arms (2)
Eccentric Exercise Program
EXPERIMENTALElite athletes with grade II hamstring strain will undergo a structured rehabilitation protocol consisting of eccentric strengthening exercises. The program is designed to improve hamstring flexibility, strength, dynamic balance, and facilitate safe return to sport.
Concentric Exercise Intervention
EXPERIMENTALElite athletes with grade II hamstring strain will undergo a structured rehabilitation protocol consisting of concentric strengthening exercises. The program is designed to enhance hamstring flexibility, muscle strength, dynamic balance, and assist in safe return to sport.
Interventions
This study's interventions are distinguished by the specific application of eccentric and concentric exercise programs tailored for elite athletes with grade II hamstring strains.
This study's interventions are distinguished by the specific application of eccentric and concentric exercise programs tailored for elite athletes with grade II hamstring strains.
Eligibility Criteria
You may qualify if:
- Participants over 18 ,who are elite athlete and contunie currently active sports life,and . Those with MRI findings showing hamstring grade II strain,who does not have any systemic or mental disease volunteerly participated in the study.
You may not qualify if:
- Participants who are having severe visual impairment and perception impairment, who has pain preventing to test,who has neurologic problems ans who has a history of injury for 6 months were excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
HANTAL
Istanbul, Kartal, 34755, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst.Prof
Study Record Dates
First Submitted
August 20, 2025
First Posted
August 27, 2025
Study Start
February 20, 2018
Primary Completion
January 1, 2024
Study Completion
June 17, 2024
Last Updated
August 27, 2025
Record last verified: 2025-08