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Chronic Stroke clinical trials

View clinical trials related to Chronic Stroke.

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NCT ID: NCT05689502 Not yet recruiting - Chronic Stroke Clinical Trials

intenSive UpPer Extremity Recovery Program for Chronic Stroke (SUPER)

SUPER
Start date: February 6, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to Investigate the feasibility of a high-quality, high-dose, high-intensity upper extremity therapy program and to assess the treatment effects of a high-quality, high-dose, high-intensity upper extremity therapy program on functional outcomes, motor impairment, and quality of life

NCT ID: NCT05679700 Recruiting - Chronic Stroke Clinical Trials

The Effect of Rigid Taping in Chronic Stroke Patients With Knee Hyperextension

Start date: December 20, 2022
Phase: N/A
Study type: Interventional

In this study, it is aimed to examine the effect of rigid taping on hyperextension control in stroke patients with knee hyperextension in the stance phase of gait. Hypothesis Ho: Rigid taping has no effect on the control of knee hyperextension in stroke patients. H1: Rigid taping has an effect on the control of knee hyperextension in stroke patients.

NCT ID: NCT05679011 Not yet recruiting - Stroke Clinical Trials

6 and 10 Meters WalkTest Acceleration Distance in Stroke Survivors

Walk-test
Start date: January 30, 2023
Phase:
Study type: Observational

Introduction: Gait speed is currently used to predict the future functional status of the patient or to evaluate the improvements produced by different neurorehabilitation treatments. There is no common agreement among researchers and clinicians as to the best distance required to accelerate and decelerate and the optimal distance to time walking speed in people in the chronic phase of stroke. Objectives: The main objective is to analyze whether the 6-meter walk test (6-MeWT) with one meter for acceleration and one for deceleration is optimal as well as 2 meters for acceleration and deceleration in the 10-meter walk test (10-MWT) both at maximum and comfortable or usual speed for patients who have suffered a stroke in the chronic phase (> 6 months). The secondary objective is to evaluate whether the 10-meter walk test (10-MWT) with two meters for acceleration and deceleration is comparable to the 6-MeWT with one meter for acceleration and one meter for deceleration for a correct measurement of gait in patients who have suffered a stroke in chronic phase (> 6 months). Methods: A cross-sectional observational study will be performed. The results of the 6-MeWT with a one-meter zone for acceleration and a one-meter zone for deceleration will be compared with the 10-meter gait test (10-MWT) with 2 meters for acceleration and 2 meters for deceleration. The patient will have 8 sensors applied to different parts of the body. The two tests are performed first at a comfortable gait and second at the fastest gait that the patient can safely perform. There will be 3 repetitions for each of the tests. The patient will be randomized to start with either the 6 MeWT or the 10 MWT test. All tests will be performed on the same day. One researcher will perform the timing measurements, another will count the number of steps and another will record the signal sent by the cameras, which record the movement of the sensors. Discussion: This study will shed light on what is the optimal distance required for acceleration and deceleration in the 6 MeWT and 10 MWT walking tests and whether the two tests are comparable.

NCT ID: NCT05667480 Not yet recruiting - Chronic Stroke Clinical Trials

VR and Script Training of PWA

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

The goal of this intervention study is to investigate the effects of immersive virtual reality in rehabilitation of language and communication of individuals with post-stroke aphasia. The main research questions are: 1. Is VR-based script training a feasible treatment to Cantonese-speaking PWA? 2. Will VR-based script training, when compared to conventional script training, better enhance treatment outcomes in functional communication of PWA? Participants will be assessed before, in the middle of, immediately after treatment and 8-week post treatment in terms of their performance on: 1. Accuracy and time for producing trained scripts. 2. Accuracy and time for producing un-trained scripts 3. Standardized aphasia test on severity of language impairment 4. Standardized aphasia test on functional communication The participants will be randomly allocated to receive one of the treatment: 1. Virtual reality-based computerized script training; or 2. Computerized script training without virtual reality Researchers will compare the treatment outcomes of the two treatment conditions and see if treatment with virtual reality would better promote outcomes when compared to training without virtual reality.

NCT ID: NCT05659875 Recruiting - Chronic Stroke Clinical Trials

CompARing Long terM Outcomes in Chronic Stroke Survivors Across Investigational Assessments Following a Prescribed Upper Extremity Exercise Program

Start date: September 8, 2022
Phase: N/A
Study type: Interventional

The purpose of the study is to compare assessments of arm function following a standard exercise program in chronic stroke patients.

NCT ID: NCT05615610 Not yet recruiting - Chronic Stroke Clinical Trials

Effects of Transcutaneous Electrical Nerve Stimulation on Cognitive Function and Upper Limb Motor Function in People With Chronic Stroke

Start date: December 1, 2022
Phase: N/A
Study type: Interventional

Upper limb impairment is present in more than 85% of people with stroke, which greatly affect the quality of life, social participation, and performance of daily activities of people with stroke. Previous study also revealed that 53.4% of people after stroke experienced cognitive impairment. Different cognitive domains might be affected following stroke, such as attention, memory, language, and orientation, and the problems with memory are often prominent. Yet, there is no effective treatment for the post-stroke cognitive impairment. Transcutaneous electrical nerve stimulation (TENS) applied on thoracic region and transcutaneous vagus nerve stimulation (tVNS) are simple and non-invasive treatment to improve upper limb motor function and cognitive function. However, no existing studies have explored on the effects of TENS and tVNS on cognitive function in people with stroke. Therefore, the purpose of this study is to evaluate the effectiveness of TENS on improving upper limb function and cognitive function in people with chronic stroke. Also, this study will investigate the cortical response of people with stroke during TENS by using EEG power spectrum analysis.

NCT ID: NCT05591196 Recruiting - Stroke, Ischemic Clinical Trials

Hand and Arm Motor Recovery Via Non-invasive Electrical Spinal Cord Stimulation After Stroke

HARNESS
Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The recovery from a stroke is often incomplete. It is the leading cause of acquired permanent disability in the adult population. Persistent functional loss of the hand and arm contributes significantly to disability. However, the current standard of care to treat hand and arm movements are inadequate. There is an urgent need for innovative and effective therapies for recovery of the upper limb after stroke. Growing evidence shows that electrical spinal cord stimulation, combined with activity-dependent rehabilitation, enables voluntary movement of paralyzed muscles in some neurologic disorders, such as spinal cord injury. The investigators hypothesize that spinal networks that lost control after stroke can be activated by non-invasive electrical stimulation of the spinal cord to improve functional recovery. The aims of the study are: 1. to determine the improvements in hand and arm function that result from the combined application of non-invasive spinal stimulation and activity-based rehabilitation. Surface electrodes placed over the skin of the neck will be used for non-invasive electrical stimulation of the spinal cord. Functional task practice will be used for activity-dependent rehabilitation, 2. to evaluate long-lasting benefits to hand and arm function that persist beyond the period of spinal stimulation.

NCT ID: NCT05581602 Not yet recruiting - Chronic Stroke Clinical Trials

Actimetry Monitoring of the Paretic Upper Limb in Chronic Post Stroke.

ParUse
Start date: November 7, 2022
Phase: N/A
Study type: Interventional

After a stroke, 80% of patients continue to have difficulty using their paretic upper limb in activities of daily living (ADL) despite post-stroke rehabilitation practices that aim to promote the use of the paretic upper limb. It is known that functional recovery depends on actual use (Use it or Loose it), but one-time measurements in the clinic do not allow quantification of the actual use of the paretic upper limb in daily life (in the person's living environment). The investigators hypothesize the feasibility of quantifying functional use of the paretic upper limb by actimetry in clinical routine.

NCT ID: NCT05526859 Recruiting - Chronic Stroke Clinical Trials

Effect of Kinesiotape Technique on Wrist Among Chronic Stroke Patients

Start date: August 31, 2022
Phase: N/A
Study type: Interventional

The aim of this randomized controlled is to assess the effect of kinesiotape technique upon wrist joint among the patients with chronic stroke. Patients are devided into groups, in group A kinesiotaping facilitation technique is applied on wrist extensor muscles while inhibition technique is applied on wrist flexor muscles and the result is the compared between the groups and within the group.

NCT ID: NCT05490277 Not yet recruiting - Chronic Stroke Clinical Trials

Vibrotactile Coordinated Reset for the Treatment of Chronic Stroke

Start date: December 1, 2022
Phase: N/A
Study type: Interventional

The purpose of our study is to evaluate Vibrotactile Coordinated Reset stimulation (vCR) and its effects on motor ability within stroke patients. vCR will be administered with a device called the Vibrotactile (VT) Brain Glove. vCR is expected to provide patients with a non-invasive therapy to aid in recovery in stoke patients This study will include a dedicated sham that will aid in understanding true treatment effects from vCR