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Upper Extremity Problem clinical trials

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NCT ID: NCT05931133 Not yet recruiting - Clinical trials for Upper Extremity Problem

Urdu Translation and Validation of Michigan Hand Outcome Questionnaire

Start date: July 1, 2023
Phase:
Study type: Observational

Aim of this study to provide a urdu version of Michigan Hand Outcome Questionnaire, that will be more understandable for Pakistani People.

NCT ID: NCT05883488 Recruiting - Cerebral Palsy Clinical Trials

Effectiveness of Robot-Assisted Upper Extremity Rehabilitation in Children With Cerebral Palsy

Start date: July 19, 2023
Phase: N/A
Study type: Interventional

The use of robotic rehabilitation, a treatment method for improving the motor functions of the upper extremities, is gradually increasing in children with cerebral palsy. The aim of this study is to investigate the effect of robot-assisted rehabilitation for the upper extremity on upper extremity functions, manual skills and quality of life in patients with unilateral or bilateral/triplegic spastic cerebral palsy and also to compare the effect of robot-assisted upper extremity rehabilitation compared to traditional rehabilitation methods.

NCT ID: NCT05872646 Completed - Clinical trials for Cognitive Impairment

The Effect of Cognitive Functions on Upper Extremity Functionality in Parkinson's Patients

Start date: February 8, 2018
Phase: N/A
Study type: Interventional

Parkinson's Disease (PD), first described by James Parkinson in 1817, is a progressive movement disorder that develops mainly as a result of the destruction of nigrostriatal dopaminergic neurons. The aim of our study is to determine the effect of cognitive functions on upper extremity functionality in individuals with Parkinson's Disease.

NCT ID: NCT05821257 Completed - Multiple Sclerosis Clinical Trials

Arm Swing During Walking in Early Multiple Sclerosis

Start date: December 1, 2021
Phase:
Study type: Observational

Multiple sclerosis (MS) is the most common central nervous system inflammatory demyelinating disease which causes motor and sensory deficits, cerebellar symptoms, and balance problems. Due to these symptoms, gait abnormalities are common in MS, even in patients with low degrees of impairment. The upper limb has an important role on postural control and gait stability. Affected arm swing movement and asymmetry during gait are common in neurological disorders such as Parkinson's disease (PD) even in early stages of the disease and arm swing treatment has been acknowledged to enhance gait and normalize arm swing in individuals with PD. The presence of arm swing changes during walking in MS patients, similar to PD, especially in the early period, may be an indicator of balance problems, this was, however, not investigated as such. Therefore, the aim of the current study is to assess the arm swing during gait in people with MS shortly after their diagnosis in early MS.

NCT ID: NCT05799391 Recruiting - Clinical trials for Upper Extremity Problem

RCT for the Efficacy of Soothing Cream Jel in Improving Upper Limb Pain and Motion

Start date: July 10, 2023
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blinded, placebo-controlled clinical trial. This trial is used to evaluate the efficacy of soothing cream jel on chronic upper limb pain and the range of motion.

NCT ID: NCT05696535 Not yet recruiting - Motor Activity Clinical Trials

Investigation of the Relationship Between Lower and Upper Extremity Selective Motor Control and Sensory Functions in Children With Spastic Cerebral Palsy

Start date: January 2023
Phase:
Study type: Observational

Although spasticity, contractures and muscle weakness in children with CP are disorders that can be observed more easily and are more focused and given more importance in evaluation and treatment approaches; Inadequate or loss of selective motor control negatively affects motor functions to a greater extent. It is very important to reveal the causes and consequences of selective motor disability in children with spastic cerebral palsy, in terms of creating effective treatment plans. The number of patients to participate in the study was determined as 100. The study will be carried out in Hatay Mustafa Kemal University Research and Application Hospital, Department of Pediatrics. In our study, demographic information will be filled in, and lower extremity selective control assessment scale (SCALE) for lower extremity, upper extremity selective control scale (SCUES) for upper extremity, and sensory assessment (touch, two-point discrimination and proprioceptive sensory assessment) will be performed on the patients who accepted the study.

NCT ID: NCT05691023 Recruiting - Ischemic Stroke Clinical Trials

VNS-REHAB At-Home - Post-Market Study for Using the Vivistim System® at Home

AT-HOME
Start date: June 1, 2023
Phase:
Study type: Observational

This is a single-arm post-market study of up to 150 participants, using up to 50 mobile therapists to conduct up to 36-hours at-home therapy. The study will assess at-home therapy implementation instead of an in-clinic therapy implementation for patients who are commercially implanted with the Vivistim System. Patients will be consented for eligibility if appropriate to be implanted with the Vivistim System per the indications for use (The MicroTransponder® Vivistim® Paired VNS™ System is intended to be used to stimulate the vagus nerve during rehabilitation therapy in order to reduce upper extremity motor deficits and improve motor function in chronic ischemic stroke patients with moderate to severe arm impairment.). Study participation includes receiving rehabilitation therapy paired with VNS, provided at the patient's home by a therapist, along with self-activated VNS. All subjects will be commercially implanted with the Vivistim System® after an ischemic stroke prior to Study treatment, although they may be consented prior to implant. It should be noted that the implant surgery is not part of the study.

NCT ID: NCT05662878 Completed - Stroke Clinical Trials

Evaluation of Hand Strength and Spasticity in Hemiplegic Patients

Start date: October 15, 2022
Phase:
Study type: Observational

The aim in this study is to evaluate spasticity and hand grip strength with a finger hand robot in the Turkish population.

NCT ID: NCT05651139 Not yet recruiting - Clinical trials for Upper Extremity Problem

Vibration Device Effect on Post-Injection Pain in The Upper Extremity

Start date: January 20, 2023
Phase: N/A
Study type: Interventional

Background: Vibratory stimulation is one of several non-pharmacological techniques used to reduce pain. Local vibration therapy generates vibrations that can penetrate up to 6 centimeters into the tissue and is utilized to manage muscle tone, alleviate localized pain, and induce an increase in blood and lymphatic circulation. This therapy is most commonly used to treat chronic pathologies of the muscles, tendons, and joints. A few studies investigating the effects of local vibration therapy on skeletal muscles and joints have found it to be beneficial in improving joint mobility and decreasing pain. Previous reports have indicated that whole-body vibration can suppress chronic low back pain, knee osteoarthritis, and peripheral neuropathy. The aim of this study is to evaluate the effects of the application of vibration stimulation on upper extremity injection-induced pain and satisfaction. Objectives: The purpose of this study is to assess the effect of vibration stimulation application on upper extremity injection pain and satisfaction. Methods: An electrical massage kit that induces vibration will be used on adult patients who are scheduled to receive local anesthesia or corticosteroid injections in their upper extremities. Two validated scales will be used to first assess the pain after the injection and the patient's satisfaction following the use of the vibration device.

NCT ID: NCT05338229 Withdrawn - Clinical trials for Upper Extremity Problem

Kinect Sensor in Cerebral Palsy Children: Phase 2.1

Start date: June 2022
Phase: N/A
Study type: Interventional

There are 3 phases of the study. This registration is phase 2.1.This registration will conduct a pilot study in the cerebral palsy children.