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Stroke Rehabilitation clinical trials

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NCT ID: NCT03834311 Completed - Hemiplegia Clinical Trials

The Effectiveness of Upper Extremity Isokinetic Strengthening in Post-stroke Hemiplegia

Start date: February 21, 2019
Phase: N/A
Study type: Interventional

This randomised controlled study will investigate the effectiveness of isokinetic strengthening on the upper extremity functionality and strength in post-stroke hemiplegic patients.

NCT ID: NCT03798340 Completed - Clinical trials for Stroke Rehabilitation

Vibratory Perturbation-based Pinch Task Training for Stroke Patients

Start date: March 24, 2016
Phase: N/A
Study type: Interventional

The investigator assumed that perturbed-event-induced vibrotactile cueing enable more precision arm movement adjustment, sensory function and dexterity improvement in the spastic arm. Thus the specific aim of the study was to develop a vibrotactile therapy system that can provide vibrotactile feedback through the pinch performance of the hand when countering mechanically induced perturbations and also analyzed training effects of the perturbation-based pinch task training system on the sensorimotor performance of the hands for stroke patients.

NCT ID: NCT03773653 Completed - Clinical trials for Stroke Rehabilitation

Synergistic Bilateral Upper-Limb Stroke Rehabilitation Based on Robotic Priming Technique

Start date: November 12, 2018
Phase: N/A
Study type: Interventional

This comparative efficacy study will be based on a 3-armed controlled trial: bilateral robotic priming combined with bilateral arm training (bilateral RT+BAT), bilateral robotic priming combined with mirror therapy (bilateral RT+MT), and the control intervention (bilateral RT+IOT). The goal of this 4-year project is to provide scientific evidence of the comparative efficacy research of hybrid interventions based on unilateral vs. bilateral approach to upper limb rehabilitation in subacute and chronic stroke.

NCT ID: NCT03319992 Completed - Chronic Disease Clinical Trials

Upper Limb Task-Oriented Rehabilitation With Robotic Exoskeleton for Hemiparetic Stroke Patients

RH-LEXOS
Start date: July 20, 2016
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the effects of an assisted rehabilitation treatment through a robotic exoskeleton device on the functional recovery in a group of patients with hemiparesis from lesion of the first motor neuron (post-stroke), compared with a group of patients subjected to a conventional rehabilitation treatment. The patients enrolled in the study are chronic stroke injured with right hemiparesis of moderate to severe degree, by the system injury pyramid, never undergoing rehabilitation treatment with robots.

NCT ID: NCT03318341 Completed - Stroke Clinical Trials

TheraBracelet Phase I

Start date: January 9, 2018
Phase: N/A
Study type: Interventional

This project aims to test a new technology that may improve hand function impaired from a stroke, thereby improving independence and quality of life.

NCT ID: NCT03279848 Completed - Clinical trials for Stroke Rehabilitation

Stratification of Stroke Rehabilitation: 5-year Profiles of Functional Outcomes

Start date: January 1, 2011
Phase: N/A
Study type: Observational [Patient Registry]

Objective: To make use of admission Modified Functional Ambulation Category (MFAC) as a stratification tool to reveal profiles of functional outcomes of patients with stroke in inpatient rehabilitation. Design: This was a retrospective, descriptive study of the demographic, functional outcomes of patients with stroke in an inpatient rehabilitation centre. A total of 2,722 patients completed a stroke rehabilitation program from 2011 to 2015 were recruited.

NCT ID: NCT03165630 Completed - Stroke Clinical Trials

Stroke Patients' Outpatient Rehabilitation Therapy (SPORT)

SPORT
Start date: May 26, 2017
Phase: N/A
Study type: Interventional

Background: Stroke is the leading cause of long-term disability in Singapore, and studies have found that intensive specialized stroke rehabilitation can improve post-stroke functional outcomes for a substantial proportion of stroke patients. However, despite the benefits associated with adherence to prescribed rehabilitation, the uptake rate of outpatient rehabilitation services (ORS) in Singapore is only 33%. According to local longitudinal studies, the financial burden of out-of-pocket service costs and the inconvenient transportation from home to rehabilitation centres are important barriers to access to ORS. Objective: To examine the effect and cost-effectiveness of providing incentives for ORS to improve the uptake of ORS compared to usual care (control) with no incentives Hypothesis: An evidence-based program to test the effectiveness of providing incentives to alleviate the financial burden as well as inconvenience of transportation for ORS will improve the uptake of and adherence to ORS among stroke patients. Methodology: This study is an individual-based randomized controlled trial (RCT) of 300 stroke patients recruited from Singapore General Hospital (SGH) and Changi General Hospital (CGH). They will be randomized to one of three study arms (education only, free transportation, and free services and transportation) and interviewed at the time of recruitment and four months after the enrolment in the study. Participants' health conditions, socioeconomic situation, health & medical services utilization, stroke-related disability measures, quality of life, and reasons for uptake/rejection/withdraw from the services will be collected during both baseline and the 4th month assessments. Significance: As the first study in Singapore to test innovative ways to increase the stroke ORS uptake rates, it will provide evidence for future policy changes in financing outpatient rehabilitation and other long-term care services in Singapore. It will also provide important empirical parameter estimates for Systems Dynamics modelling of the demand and supply of ORS in Singapore.

NCT ID: NCT03044080 Completed - Clinical trials for Stroke Rehabilitation

Effects of Botulinum Neurotoxin Type A (BoNT/A) Free of Complexing Proteins in the Spastic Equinovarus Foot

Start date: January 1, 2015
Phase: Phase 4
Study type: Interventional

Clinical randomized clinical trial to assess the effectiveness on walking speed of repeated use of botulinum neurotoxin type A (BoNT/A)in the post-stroke spastic equinovarus foot in three successive infiltrations at 6-month intervals, checking if the sustainability of the effect is greater in incobotulinumtoxin A (Xeomin®) than in onabotulinumtoxinA (Botox®).

NCT ID: NCT03031977 Completed - Clinical trials for Stroke Rehabilitation

Visceral Mobilization and Functional Constipation in Stroke Survivors

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

The aim of the present study was to evaluate the effect of visceral mobilization on symptoms of functional constipation and static balance in stroke survivors.

NCT ID: NCT03023150 Completed - Clinical trials for Stroke Rehabilitation

Ischemic Preconditioning as an Intervention to Improve Stroke Rehabilitation - Froedtert

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

This study will be the first study to use ischemic preconditioning (IPC) as an intervention to improve stroke rehabilitation. IPC is a well studied, well tolerated intervention which has been shown to improve regional blood flow, motor neuron excitability and muscle function in multiple patient groups and in young, healthy subjects. Because IPC targets three physiological systems which are all affected by stroke, we hypothesize that repeated bouts of IPC during the first days to months following stroke (when the majority of recovery occurs) will make traditional rehabilitation strategies more effective.