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Rehabilitation clinical trials

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NCT ID: NCT03857529 Recruiting - Stroke Clinical Trials

Improving Stroke Motor Control With Non-invasive Brain Stimulation and Functional Electrical Stimulation

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

This pilot study for stroke patients with chronic upper limb hemiplegia will examine the effects of non-invasive brain stimulation and neuromuscular electrical stimulation on hand motor control and corticospinal excitability. Specifically, this study will investigate the effects of timing and delivery of tDCS in conjunction with contralaterally controlled functional electrical stimulation.

NCT ID: NCT03856983 Completed - Rehabilitation Clinical Trials

Benefits of Observing Point-light Displays in Postoperative Rehabilitation of the Total Knee Prosthesis.

LOARAL
Start date: January 14, 2020
Phase: N/A
Study type: Interventional

The LOARAL project concerns patients who have undergone total knee arthroplasty to treat symptomatic osteoarthritis. Patient will be divided into two groups: a control group where patients will do standard rehabilitation and an experimental group where patients will do standard rehabilitation associated with the judgement of point-light display. The aim of this study is to validate the use of point-light display for the Rehabilitation of patients with a totalarthroplasty of the knee.

NCT ID: NCT03847454 Completed - Rehabilitation Clinical Trials

REACH Personal Mobility Device Testing

REACH
Start date: February 27, 2019
Phase: N/A
Study type: Interventional

Developed countries are facing the challenge of ageing societies, lack of infrastructure for healthcare and high cost of care. Researchers have been attempting to answer these problems by using innovative technology to promote healthy ageing. In this trial, the investigators test the efficiency and acceptance of a personal mobility device for elderly physical rehabilitation. The main objective of the study is to investigate whether rehabilitation using the mobility equipment is as effective as the standard care; secondly, to determine if there is an improvement in clinical outcomes such as physical strength, balance, and risk of falls after using the mobility equipment; and third, to establish whether the use of the REACH concept adds value to the continuity of patient care, specifically in terms of engagement and motivation to be more active during the hospital stay and when returning home.

NCT ID: NCT03825770 Completed - Quality of Life Clinical Trials

Pilot Study of an Educational Program for Adults on Hemodialysis With Fatigue

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

Fatigue is a common and problematic symptom of end-stage renal disease (ESRD). The investigators have developed a new program, called the Personal Energy Planning (PEP) program, that teaches people with ESRD to manage fatigue by using energy conservation strategies during everyday life (eg. organization, prioritization, using good body postures and assistive tools). A large study is needed to test whether the program is helpful for people with ESRD. First, the investigators need to do a smaller-scale pilot study to help plan the large study. The main purposes of this pilot study are to see how many people with ESRD are willing and able to complete the PEP program, and to explore whether the program helps people feel less fatigued. The investigators plan to invite 40 people with ESRD from 4 dialysis units in Calgary, Alberta to participate. People with ESRD who report feeling unusually tired a lot of the time (using a symptom assessment tool completed every 2 months) will be asked to take part. Study participants will either do the PEP program, or another program (the control) that gives them general information about kidney disease. Participants will also be asked to complete questionnaires about fatigue before and after the study. The investigators will compare fatigue scores between the PEP program group and the control group, and record how many agree to take part in the study and complete all study activities. This pilot study will help the investigators plan next steps for research into the PEP program.

NCT ID: NCT03815994 Suspended - Rehabilitation Clinical Trials

Neuromuscular Electrical Stimulation in Critically Ill Patients.

Start date: November 13, 2018
Phase: N/A
Study type: Interventional

The study will investigate the effects of neuromuscular electrical stimulation (NMES) in critically ill patients. The objective of this study will be investigate the effects of neuromuscular electrical stimulation (NMES) in critically ill patients.

NCT ID: NCT03801460 Recruiting - Frailty Clinical Trials

Physiological Reconditioning Program Administered Remotely in Patients Undergoing Transcatheter Aortic Valve Replacement: A Pilot Study

PREPARE-TAVR
Start date: July 1, 2020
Phase: N/A
Study type: Interventional

The PREPARE TAVR pilot study will examine the effects of remotely administered physiological reconditioning program (RAPR) on quality of life (QOL) and clinical outcomes at one year post TAVR in frail older adults.

NCT ID: NCT03789305 Completed - Critical Illness Clinical Trials

Differences in Frail and Non-frail Critically-ill Patients in Functional Outcomes

DEFAULT
Start date: April 1, 2017
Phase:
Study type: Observational

This is a prospective analysis of patient registry data of intensive care patients. The aim is to investigate if frailty is a predictor of decline of functional status of critically ill patients during their hospital stay.

NCT ID: NCT03771872 Terminated - Stroke Clinical Trials

Virtual Prism Adaptation Therapy on Hemispatial Neglect

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

The purpose of this study is to investigate the effect of virtual prism adaptation therapy on hemispatial neglect in chronic stroke patients. This study is the randomized, double-blind, sham-controlled, cross-over design. Total 10 patients will be allocated randomly to either real virtual prism adaptation therapy or sham therapy with the wash-out period of more than 2 weeks. Two sessions (20min/session) per day, for 5days (total 10 sessions) will be provided. Behavioral outcomes will be measured before and after completing a total of 10 sessions therapy.

NCT ID: NCT03769636 Recruiting - Rehabilitation Clinical Trials

Changes in Physical Activity in All Day Life in People With MS Before and After Rehabilitation

Start date: January 1, 2018
Phase:
Study type: Observational

The primary objective is to observe the impact of in-patient rehabilitation on physical activity in daily life using miniature, wearable sensors, fixed on the shoes. These sensors record data about various aspects of walking. The information on the therapy effect on daily life can complement the clinical information and the patients' subjective report on therapy induced improvements. The secondary objective is the association of changes in physical activity, self-rated walking capacity, self-rated fatigue and self-rated health-related quality of life, wich will be analysed for disease severity of the participants.

NCT ID: NCT03764982 Active, not recruiting - Rehabilitation Clinical Trials

RehabNytte - A Study of Rehabilitation Processes in Specialized Care in Norway

Start date: January 2, 2019
Phase:
Study type: Observational

The main objective of the study is to describe function and health related to quality of life during the first year after rehabilitation, to measure the degree and impact of user involvement in the rehabilitation process, assess factors associated with change in work -ability and -participation, and to test measurement properties of a new core set of outcome measures for rehabilitation launched by the Norwegian Directorate of Health.