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Knee Injuries clinical trials

View clinical trials related to Knee Injuries.

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NCT ID: NCT03130400 Completed - Knee Injuries Clinical Trials

Kinematic Parameters to Predict Knee Diseases.

Start date: April 20, 2017
Phase: N/A
Study type: Observational

There is no study to explore the prediction of knee diseases using kinematic parameters of knee during gait. The aim of this study is to explore the possibility of predicting knee diseases by gait parameters.

NCT ID: NCT03117205 Completed - Knee Injuries Clinical Trials

The Effect of Kinesio Taping® on Motor Control in Patients With Patellofemoral Pain Syndrome

Start date: December 10, 2014
Phase: N/A
Study type: Interventional

Background: Recently, several professionals are using the Kinesio Taping® in the treatment of pathologies related to the knee, aiming to improve the motor control, increase the response of muscle activation and promoting better joint stability. Purpose: The objective of this study is to evaluate the effect of the application of Kinesio Taping® in motor control of patients with patellofemoral pain syndrome. Methods: This is a 2-arm, randomized with a blinded assessor. We selected 40 women with patellofemoral pain (age 25.2±4,years) were randomly assigned to one of two groups: placebo group (n= 20) and the Kinesio Taping® group (n=20). The placebo group received the application of a non-stretchable tape (Micropore) crosswise on the thigh and the Kinesio Taping® group followed all the criteria of the method in placing the bandage. All patients received the evaluation of the motor control banding pre and post a patch, by means of the method Y balance test.

NCT ID: NCT03116230 Completed - Knee Osteoarthritis Clinical Trials

Gait Modification Treatments for Knee Pathology

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

The objective of this study is complete a longitudinal cross-over clinical study to investigate the effect of treatments for knee pathology, including cutaneous stimulation (skin vibration and soft knee brace), on locomotion tasks (i.e. walking, jogging, stair ascending and descending), muscle function, and pain/function.

NCT ID: NCT03063814 Completed - Clinical trials for Musculoskeletal Injury

Effects of App-based Versus Personal On-site Instruction on Neuromuscular Activity in Injury Prevention Exercises

ACL01
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

Therefore, the aim of the present study was to evaluate neuromuscular characteristics observed during a single bout of selected and validated injury preventive exercises instructed by an app (in accordance with 'Get set - Train smarter') versus gold standard instruction, supervision and feedback provided on-site by an expert. The present evaluation targets a population of female football and handball players without any previous exposure to injury prevention training.

NCT ID: NCT03035266 Completed - Knee Injuries Clinical Trials

The Effect of Blood Flow Restriction Training on Muscle Atrophy Following Knee Surgery

Start date: April 5, 2017
Phase: N/A
Study type: Interventional

The investigators will compare differences in quadriceps strength, leg girth, and functional outcome scores between two groups of patients after weeks 6 and 12 as well as 6 months following meniscus or articular cartilage repair/restoration requiring 6 weeks of non-weight bearing or limited weight bearing status in a brace at 0° degrees of knee extension. One group will receive BFR with standard post-operative rehabilitation for 12 weeks followed by the standard protocol progression for the remainder of the treatment program. The other group will receive standard post-operative rehabilitation without BFR for the duration of treatment program.

NCT ID: NCT02997644 Completed - Opiate Addiction Clinical Trials

Impact of Different Educational Approaches on Post-operative Opiate Utilization After Elective Lower Extremity Surgery

OpiateLEO
Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of post-operative opioid use after two different educational interventions. The investigators will compare changes in pain, disability and sleep between groups 6 months after elective lower extremity surgery.

NCT ID: NCT02937064 Completed - Osteoarthritis Clinical Trials

Multimodal Assessment of Knee Conditions

MAKnee
Start date: November 2016
Phase: N/A
Study type: Observational

The purpose of this study is to assess both osteoarthritis and other pathological knee conditions from the combination of signals that are known to provide information on the knee joint.

NCT ID: NCT02882152 Completed - Knee Injuries Clinical Trials

Femoral/Sciatic Block for Knee Surgery

Start date: August 2011
Phase: N/A
Study type: Interventional

Knee arthroplasty has a high potential for postoperative pain. This study compares analgesia and postoperative bleeding from intrathecal morphine with the continuous femoral and a single-shot sciatic nerve blockades.

NCT ID: NCT02804685 Completed - Knee Injuries Clinical Trials

Effectiveness of an Exercise Protocol on Alteration of Knee Joint Position Sense in Futsal Players

Start date: June 2016
Phase: N/A
Study type: Interventional

This research presents a randomized clinical trial which evaluates the effectiveness of an exercise protocol on the knee-joint repositioning in futsal players related to a post-match muscle fatigue. Our hypothesis is the improvement of sensation in a knee in joint position before and after the match when performing our exercise program.

NCT ID: NCT02754700 Completed - Knee Injuries Clinical Trials

Real-time Optimized Biofeedback Utilizing Sport Techniques

ROBUST
Start date: April 2016
Phase: Phase 2
Study type: Interventional

This study will identify the most optimal, focused approach for biofeedback in adolescent females at high risk for anterior cruciate ligament (ACL) injury. A six-week randomized, pre/post-testing design will be used to identify biofeedback training effects. The investigators will also determine the effects of hip strategy on retention of decreased knee abduction load with focused biofeedback. A six-month follow-up design will be used to test retention of real-time biofeedback intervention.