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Stroke clinical trials

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NCT ID: NCT05931172 Recruiting - Stroke Clinical Trials

Comparative Effects of Dual Task and PNF on Balance ,Cognition and Motor Function in Chronic Stroke Patients .

Start date: February 25, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effect of dual tasking and proprioceptive neuromuscular facilitation on balance, cognition and motor function in chronic stroke patients. It will be randomized clinical trial.

NCT ID: NCT05929287 Recruiting - Stroke Clinical Trials

Comparing Personalized and Adaptive Cognitive Training Methods Following Stroke

Start date: May 2, 2023
Phase: N/A
Study type: Interventional

This study aims to assess the efficacy of two cognitive training programs - one tablet-based (NeuroAIreh@b) and one in paper-and-pencil format (Task Generator) - in improving cognitive and noncognitive outcomes among community-dwelling stroke survivors. This study will include a waiting-list control group to assess the impact of these interventions and provide further insights into their potential for stroke survivors.

NCT ID: NCT05929027 Recruiting - Stroke Clinical Trials

Self-Administered Gaming and Exercise at Home (SAGEH)

SAGEH
Start date: September 28, 2023
Phase: N/A
Study type: Interventional

This study aims at comparing manual function outcomes between the standard of care and additional self-administered hand therapy after stroke. Strokes are common neurological injuries, and although rates of survival have increased in recent decades, survivors often continue to experience deficiencies in hand dexterity and bimanual function. Most motor recovery takes place within the first 3 months after a stroke. This initial period is necessary for stabilizing the patient but also provides different opportunities to foster motor recovery. Functional gains, including instances after the post-acute period, have been observed after regular and frequent (high dosage) therapy, suggesting that recovery is likely influenced by practice-driven sensorimotor learning. These findings motivate the implementation of daily therapeutic regimes beyond post-stroke hospitalization and basic motor function, aiming instead at addressing overlooked deficiencies in manipulation and bimanual coordination. While some hand therapy is often provided during outpatient therapy visits (the standard of care), self-administered sessions play a large role in implementing additional daily therapy. As a result, the investigators are interested in both the implementation of self-administered regimes and measuring clinical outcomes with and without self-administered therapy.

NCT ID: NCT05925231 Recruiting - Motor Activity Clinical Trials

Variability of Healthy People and People After Stroke Results in the Box and Block Test

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

Main aim of the study is to find out how many attempts of each subtest in the Box and Block Test should be done in clinical practice during testing people after stroke who are 20-64 years old.

NCT ID: NCT05924308 Recruiting - Clinical trials for Post-stroke Mild Cognitive Impairment

Acupuncture Therapy for Post-stroke Mild Cognitive Impairment: a Randomized Controlled Trial

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

1. On the basis of previous studies, standardized randomized controlled clinical trials were conducted to observe the efficacy and safety of acupuncture in the treatment of mild cognitive impairment after stroke using the international rating scale, and the clinical experience was transformed into evidence. 2. According to the clinical outcomes reported by patients, the differences between Chinese and western scales in evaluating mild cognitive impairment after stroke were compared. On the basis of "disease differentiation, syndrome differentiation and meridian differentiation", the syndrome differentiation and treatment system of mild cognitive impairment after stroke was preliminarily constructed, and the TCM syndrome prediction model was improved.

NCT ID: NCT05923931 Recruiting - Heat Stroke Clinical Trials

Non-inferiority Study of the Effect of Non-cooling Blanket on Body Temperature in Patients With Heat Stroke

Start date: May 28, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to test the cooling effect of cooling blanket in patients with heat stroke. The main questions it aims to answer are: - the cooling rate of cooling blanket in patients with heat stroke - the relationship between cooling blanket and outcomes in patients with heat stroke Participants will accept the cooling blanket or non-cooling blanket according to the randomization group. Researchers will compare cooling rate and outcomes to see if the cooling blanket can accelerate the cooling speed and improve the prognosis of patients in heat stroke.

NCT ID: NCT05923034 Recruiting - Clinical trials for Had a Computed Tomography Scan of the Chest Within 24 Hours After Stroke Onset

Pulmonary Infection After Ischemic Stroke

PICAS
Start date: March 1, 2022
Phase:
Study type: Observational

To assess the frequency of signs of pulmonary infection on a chest CT and development of clinical diagnose of poststroke pneumonia,and its effect on functional outcome in patients with acute ischemic stroke.

NCT ID: NCT05922644 Recruiting - Stroke Clinical Trials

Short-term Cervical Spinal Cord Stimulation in Patients With Disorders of Consciousness After Intracerebral Hemorrhage

SCS-ICH
Start date: July 1, 2023
Phase: N/A
Study type: Interventional

Disorders of consciousness (DOC) refers to the persistent loss of consciousness after 28 days in patients with brain injury caused by trauma, stroke, or hypoxia. It includes coma, vegetative state, and minimally conscious state. At present, there is no effective treatment for DOC. Only one RCT study of amantadine has proved that it may be effective for the treatment of DOC. In recent years, more evidence has shown that neuromodulation technology is beneficial to the recovery of DOC. Cervical spinal cord stimulation surgery is a new treatment method for patients with DOC. Electrodes are implanted in the high cervical spinal cord C2-C5. By adjusting different electrical stimulation parameters, it has a wake-promoting effect. In this study, patients were selected into the spinal cord stimulation group and the conventional treatment group according to the wishes of their families. The patients in the spinal cord stimulation group were given 21 days of cervical spinal cord stimulation treatment on the basis of conventional brain rehabilitation. Patients were followed up routinely and completed designated examinations at 12 months to determine the safety and efficacy of cervical spinal cord stimulation therapy.

NCT ID: NCT05921695 Recruiting - Heat Stroke Clinical Trials

The Relationship Between Normal Saline Infusion and Acute Kidney Injury in Heat Stroke

Start date: May 28, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the effect of high chlorine solution such as normal saline and non-high chlorine solution such as sodium lactate ringer's solution on renal function in patients with heat stroke. The main question it aims to answer is whether limiting the amount of normal saline infusion during emergency department can lower the incidence of acute kidney injury and mortality in patients with heat stroke. Participants will receive a free normal saline infusion during the emergency department according to the study design, or a restricted normal saline infusion while using sodium lactate Ringer's instead. Researchers will compare the normal saline infusion group and sodium lactate Ringer's group to see if limiting the amount of normal saline infusion during emergency department can lower the incidence of acute kidney injury and mortality in patients with heat stroke.

NCT ID: NCT05921682 Recruiting - Heat Stroke Clinical Trials

Early Body Temperature Targets and Relationship With Prognosis in Patients With Heat Stroke

Start date: May 28, 2023
Phase:
Study type: Observational

The goal of this observational study is to explore the optimal target body temperature in first 24 hours and the relationship between body temperature and adverse outcomes of heat stroke. The main questions it aims to answer are: - the optimal target body temperature at 0.5 h, 2 h, and the lowest body temperature of heat stroke. - the best body temperature at the cutting point of stop cooling. - The relationship between the volume and speed of ice saline infusion and the cooling effect.