The Effect of Contralateral Limb Training on Functional Outcomes in Patients With ACL Reconstruction
NCT ID: NCT03304561
Last Updated: 2018-02-05
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
36 participants
INTERVENTIONAL
2016-10-01
2017-10-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Blood Flow Restriction Training on Patient With Anterior Cruciate Ligament Reconstruction
NCT04284748
Effect of Different Focused Techniques on Thigh Muscle Activation After Anterior Cruciate Ligament Reconstruction
NCT05342415
Resistive Co-contraction Training After Anterior Cruciate Ligament Reconstruction
NCT02300636
Blood Flow Restriction After Anterior Cruciate Ligament Reconstruction (ACLR)
NCT05500872
Comparison of Remnant-Preserving Anterior Cruciate Ligament Reconstruction With Healthy Controls
NCT05245461
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
traditional rehabilitation
patients in this groups is going to recieve traditional rehabilitation programme for 3 months after ACL recontsruction
Traditional rehabilitation
traditional ACL rehabilitation program
Cross-over training
patients in this programme is going to recieve isokinetic exercise programme targeting unilvolved limb during rehabilitation. for the first 4 weeks after ACL reconstruction traditional rehabiitation programme is going to applied to the subjects. after 4 weeks, isokinetic strenghtening programme at 60˚/second angular velocity, between 0-90 degree knee flexion until 3 months after ACL reconstructon
Cross-over training
Cross-over training addition to the traditional rehabilidation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Traditional rehabilitation
traditional ACL rehabilitation program
Cross-over training
Cross-over training addition to the traditional rehabilidation
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* having no problem at least six month on the nonsrgical side
* recieving the rehabilitation programme at hacettepe university, physiotherapy department
Exclusion Criteria
* having revision ACL surgery
* addition of PCL or cartilage surgery addition to the ACL surgery
* not participating to the rehabilidation program regularly over 3 month after sugery
18 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hacettepe University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
GULCAN HARPUT
Phd
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sports Physiotherapy Unit
Ankara, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
123456
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.