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Tendinopathy clinical trials

View clinical trials related to Tendinopathy.

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NCT ID: NCT04480905 Completed - Clinical trials for Biomechanical Phenomena

Effect of Dynamic Taping on Landing Kinematics and Kinetics in Volleyball Players With Symptoms of Patellar Tendinopathy

Start date: July 20, 2020
Phase: N/A
Study type: Interventional

Patellar tendinopathy (PT) is the common cause of anterior knee pain, particularly in sports required repeated jumping and landing, such as volleyball. PT clinically presents as anterior knee pain and localized tenderness at the patellar tendon. To evaluate the severity of symptoms of PT, the VISA-P questionnaire is a self-administered, well-validated, and widespread assessment tool. In the long term, athletes would land with knee avoidance patterns and transfer the load to the hip joint caused further hip-related injury. Lower extremities eccentric exercise has been proven the most beneficial treatment of PT. However, the course lasts for three to six months. For athletes who are still in season, it's difficult to get the immediate effect. A newly developed biomechanical taping, dynamic tape, considered to be beneficial for load absorption during muscle eccentric contraction during landing and further normalized the lower extremities load contribution by its viscoelasticity property. However, no past research has confirmed this effect. Therefore, the aims of the study are to translate the English VISA-P questionnaire to the Chinese and to study the reliability and validity of the Chinese version. In the next part, the investigators investigate the different landing biomechanics between individuals with and without patellar tendinopathy and establish the reliability of different landing tasks, and further explore whether the dynamic tape alters landing biomechanics in volleyball players.

NCT ID: NCT04453592 Completed - Adductor Tendinitis Clinical Trials

Adductor Longus Tenotomy & the BKFO Test

Start date: November 22, 2019
Phase:
Study type: Observational

The bent knee fall out test (BKFO) is a common test for hip adductor flexibility. It is unknown whether the BKFO actually tests the the adductors or potentially hip range of motion instead. In this study, the BKFO test is performed in the operating theater before and after an adductor longus tenotomy.

NCT ID: NCT04387591 Completed - Bicep Tendinitis Clinical Trials

Fu's Subcutaneous Needling Treatment for Biceps Tendinopathy

Start date: May 20, 2020
Phase: N/A
Study type: Interventional

Biceps tendinopathy is a common cause in shoulder-pain symptoms. The major mechanism is overuse of the biceps muscles. The long-term accumulated and poor repaired trauma causes myofascial trigger points in the related muscles.We will conduct the randomized, open label experiment to evaluate the immediate, short-term, and long-term effect of Fu's subcutaneous needling (FSN).

NCT ID: NCT04385329 Completed - Tendinopathy Clinical Trials

Shock Wave Therapy for Sural Myofascial Pain Associated to Chronic Heel Pain

Start date: July 4, 2016
Phase: N/A
Study type: Interventional

The aim of this randomized controlled study in to investigate if a shock wave treatment extended to the gastrocnemius-soleus trigger points (TrP) is more effective than a standard treatment exclusively targeted at the plantar fascia in a population affected by unilateral plantar fasciitis with concomitant sural myofascial pain syndrome.

NCT ID: NCT04384874 Completed - Clinical trials for Achilles Tendinopathy

A Novel Multi-factorial Criteria-based Rehabilitation Program for Chronic Mid-portion Achilles Tendinopathy

Start date: January 29, 2020
Phase: N/A
Study type: Interventional

Sixty physically active patients (aged 18-45) with chronic mid-portion Achilles tendinopathy will be recruited to take part in the study. The patients will be diagnosed by a sports medicine doctor and an MRI scan and will be experiencing palpable Achilles pain at the time of inclusion. The patients will be randomized into either a group performing the Silbernagel combined concentric-eccentric program, or a group performing a novel multi-phase program with specific outcome measures. The study will assess the patients calf strength, reactive strength and running biomechanics at baseline, week's 6 and 12 of a rehabilitation program and be available for a 6 month, 12 month and 2 year follow-up interview. The VISA-A questionnaire will be the primary outcome measure and will be completed at each testing and follow-up session.

NCT ID: NCT04376294 Completed - Clinical trials for Achilles Tendinopathy

Using of Extracorporeal Shockwave Therapy in Treatment Of Achilles Tendinopathy

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The purpose of this study was to determine the effect of extracorporeal Shock wave therapy (ESWT) on functional activity and pain in patients with Achilles tendinopathy

NCT ID: NCT04363398 Completed - Tendinopathy Clinical Trials

Prevention of Patellar and Achilles Tendinopathies in Youth Basketball

Start date: August 10, 2016
Phase: N/A
Study type: Interventional

This study seeks to determine the prevalence of knee and ankle tendinopathies in youth basketball players, as well as determine the efficacy of a Basketball specific Neuromuscular training warm-up in reducing injuries.

NCT ID: NCT04350827 Completed - Tendinopathy Clinical Trials

PRP vs PRP Plus IGF for Patellar Tendinosis

Start date: February 25, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two different platelet-rich plasma (PRP) injections for patellar tendinosis. Aim: To perform a randomized, double blinded study comparing the clinical effect of PRP versus PRP + concentrated insulin-like growth factor (IGF) in patients with patellar tendinosis.

NCT ID: NCT04339569 Completed - Fatigue Clinical Trials

Landing Biomechanics Following Fatigue in Athletes With and Without a History of Patellar Tendinopathy

Start date: October 25, 2019
Phase:
Study type: Observational

In this case-control study, two- and three-dimensional landing biomechanics, by means of lower limb joint angles and moments (opto-electronic system with synchronised force plate), will be compared between 30 male volleyball/basketball players with a history of patellar tendinopathy and 30 healthy controls.

NCT ID: NCT04333784 Completed - Clinical trials for Rotator Cuff Tendinosis

Blood Flow Restriction Training in Patients With Shoulder Pain

Start date: December 21, 2020
Phase:
Study type: Observational

This study was planned to investigate the effect of blood flow restriction exercise training on shoulder muscle strength and muscle thickness, and to determine the change in pain and symptoms in patients with rotator cuff tendinopathy. Patients in the study group will perform the rehabilitation exercises with a pneumatic cuff and blood flow restricted. The patients in the control group will perform the same exercise program without restricting blood flow.