Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
40 participants
INTERVENTIONAL
2021-02-01
2023-08-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Plyometric Training Group
Individuals in the plyometric training group will receive plyometric training. In this training, individuals will not participate in a real plyometric training. Volunteers will watch videos to be prepared (action observation) and imagine them performing those exercises (motor imagery). Except for one session that will be applied every two weeks, all other trainings will be given on the basis of telerehabilitation via distance education tools.
Plyometric Exercise
Plyometric training consisting of ten different exercises \[vertical unilateral and bilateral counter movement jump, horizontal unilateral and bilateral counter movement jump, drop jump (30 cm), squat jump, step-hop (20 cm), 180 degree rotation in transverse plane, frontal plane hurdle jump (20 cm) and sagittal plane hurdle jump (20 cm)\] for 8 weeks, 3 sessions per week. Individuals will not participate in a real plyometric training. Volunteers will watch videos to be prepared (action observation) and imagine them performing those exercises (motor imagery)
Control Group
Volunteers in this group will not participate in any training.
No interventions assigned to this group
Interventions
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Plyometric Exercise
Plyometric training consisting of ten different exercises \[vertical unilateral and bilateral counter movement jump, horizontal unilateral and bilateral counter movement jump, drop jump (30 cm), squat jump, step-hop (20 cm), 180 degree rotation in transverse plane, frontal plane hurdle jump (20 cm) and sagittal plane hurdle jump (20 cm)\] for 8 weeks, 3 sessions per week. Individuals will not participate in a real plyometric training. Volunteers will watch videos to be prepared (action observation) and imagine them performing those exercises (motor imagery)
Eligibility Criteria
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Inclusion Criteria
* Volunteers using hamstring autograft in their ACLR
* Volunteers who have passed 1-5 years after their ACLR
Exclusion Criteria
* Those who have had revision surgery
* Those who had posterior cruciate ligament rupture in addition to anterior cruciate ligament
* Third-degree tears in the lateral or medial collateral ligaments
* Those with 2nd or 3rd degree strain injuries in hamstring and quadriceps muscle groups
* Those with a history of congenital, neurological, orthopedic, rheumatologic and cardiopulmonary pathology or anomalies,
* Those with serious systemic diseases
* Those with acute infection or pain
* Those with joint instability
* Those with a body mass index of 30 and above
* Those receiving energy supplements or ergogenic assistance during or during the 6-month period prior to work
18 Years
35 Years
ALL
Yes
Sponsors
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Hacettepe University
OTHER
Responsible Party
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Murat EMİRZEOĞLU
Physiotherapist (MSc)
Locations
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Hacettepe Üniversitesi
Ankara, Türkiye, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2020-11167
Identifier Type: -
Identifier Source: org_study_id
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