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Neurological Rehabilitation clinical trials

View clinical trials related to Neurological Rehabilitation.

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NCT ID: NCT06147726 Recruiting - Parkinson Disease Clinical Trials

Upper Extremity Rehabilitation With Virtual Reality in Parkinson's Disease Patients

Start date: November 1, 2023
Phase: N/A
Study type: Interventional

Upper extremities are the first part of the body to be affected by Parkinson's disease. Although studies have shown that virtual reality-assisted rehabilitation methods are effective on gait and balance, studies on their use for upper extremity rehabilitation are limited. For this reason, the aim of the project is to examine whether virtual reality supported upper extremity position matching exercises, which will be specially prepared according to joint ranges of motion, will provide functional improvement in the upper extremities of individuals with Parkinson's disease.

NCT ID: NCT05566782 Recruiting - Stroke Clinical Trials

Cross-sectoral Rehabilitation After Stroke (CRES)

CRES
Start date: January 23, 2022
Phase:
Study type: Observational

Prospective cohort study during post stroke rehabilitation in hospital and municipality. Participants will be measured with accelerometers, tests in relation to physical function and qualitative interviews.

NCT ID: NCT04204655 Recruiting - Clinical trials for Neurological Rehabilitation

Influence of the Body Composition of Neurological (Early) Rehabilitants on Rehabilitation Success

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

An optimal nutritional supply is associated with better outcome and recovery. For investigating the influence of the nutritional status and body composition on the course of rehabilitation, bioelectrical impedance analyzes (BIA) should be carried out on neurological (early) rehabilitants during the rehabilitation process. Possible disturbances, suitable outcome valuesfor evaluation of the rehabilitation success (depending on the rehabilitation phase) as well as the required frequency of the BIA measurements in rehabilitation should be estimated with the help of this pilot study.

NCT ID: NCT03643419 Recruiting - Clinical trials for Spinal Cord Injuries

Clinical Study of Treatment of Acute Spinal Cord Injury by Near Infrared Light Irradiation

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

The purpose of this study was to observe the therapeutic effect of near-infrared light irradiation on the treatment of acute spinal cord injury in humans, and whether it can promote the recovery of neurological function. Half of the patients underwent laminectomy and decompression surgery, and the other half of the patients were implanted with irradiated fibers for irradiation after surgery.

NCT ID: NCT03635008 Recruiting - Stroke Clinical Trials

Anodal Transcranial Direct Current Stimulation Over the Contralesional Hemisphere on Motor Recovery in Subacute Stroke Patients

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

Upper limb recovery is not predicted by the initial severity of paralysis and the parameters reflecting the integrity of the corticospinal tract (e.g. motor evoked potential, fractional anisotropy in diffusion tensor imaging). Although the inhibition of the contralesional hemisphere is known to be beneficial for the upper limb recovery after stroke in previous studies, this is not proven in the severely paralyzed upper limb. And the studies using the noninvasive stimulation in subacute stroke is lack. In addition, the role of contralesional (unaffected) hemisphere is known to be playing the important role in severe stroke. In this randomized, double-blind, sham-controlled studies, the patients with subacute stroke (<3 months after stroke onset), severe paralysis of the upper limb with poor prognosis (poor motor score and no response of motor evoked potential recorded in the extensor carpi radialis muscle) will be recruited. Interventional group will receive the 25 mins of anodal transcranial direct current stimulation (tDCS) over the contralesional premotor area plus 25 mins of robotic arm training per session for 10 sessions in 2 weeks. Control group will receive the same treatment except for sham tDCS instead of anodal tDCS over the contralesional premotor area. Functional outcome will be measured before and after the intervention (baseline, immediately after the intervention and 1 month after the intervention). Cortical activation pattern will be measured by the electroencephalography (EEG) at baseline and immediately after the intervention.