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Clinical Trials in Egypt / NCT06302946
Recruiting Not applicable

Effect of Neuromuscular Stimulation and Mindfulness Exercise in Patients With Stroke

NCT06302946 · tracked via the Priya Life Science Egypt tracker
Sponsor
Cairo University
Phase
Not applicable
Started
2026-03-15
Last updated
2026-03-13

Condition(s) studied

Stroke

Investigational drug(s) / intervention(s)

neuromuscular stimulation and mindfulnessneuromuscular electrical stimulation

neuromuscular stimulation and mindfulness: Receive neuromuscular stimulation and mindfulness breathing; the experimental group participants will receive neuromuscular electrical stimulation with Mindfulness.

neuromuscular electrical stimulation: participants in the control group perceived neuromuscular electrical stimulation

Study summary

It is an interventional study in which 60 stroke patients were estimated to enroll according to random allocation and divided into two groups. The experimental group will receive neuromuscular stimulation and mindfulness , while the control group will receive neuromuscular stimulation only.

Eligibility

Sex
ALL
Min age
50 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * The subject selection will be according to the following criteria: * All Patients of this study will be diagnosed as stroke and the diagnosis will be confirmed by computed tomography or MRI (El-Tamawy et al., 2021). * Age of patients will be ranged from 50 to 65years (males and females). * All patients will be hemodynamically stable. * Patients with good cognition that enables them to understand the requirements of the study. Exclusion Criteria: * • The potential participants will be excluded if they meet one of the following criteria: * Patients who cannot follow instructions as sensory aphasia, blindness, dementia, and deafness. * Patients with any orthopedic, neurological, or chest disorders that affect trunk muscles control or cause respiratory disorders as COPD. * Patients with cognitive and psychiatric disorders. * Patients with unstable cardiovascular conditions. * Patients with contraindications to neuro electrical stimulation as: * Cardiac pace maker. * Acute abdominal surgery.

Primary outcome measure(s)

  • ventilatory function — 12 weeks
    By a spirometer, forced vital capacity (FVC), forced expiratory volume in the first second (FEV1), the ratio of forced vital capacity to forced expiratory volume (FEV1/FVC), and peak expiratory flow will be measured.

Trial sites (1)

FacilityCityRegionStatus
Faculty of Physical Therapy Cairo Dokki Recruiting

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Other trials for the same condition

Effect of Russian Current Stimulation for Anterior Tibial Group on Postural Stability and Risk of Falling in Patients With Stroke Recruiting
Mechanical Thrombectomy in the Middle East and North Africa: Interim Results from the MEMENTO Registry Enrolling by invitation
Artificial Intelligence-Based Cognitive Training in Patients With Stroke Recruiting
Combining Transcranial Direct Current Stimulation and Core Stability Exercise on Trunk in Stroke Patient Enrolling by invitation
Telerehabilitation Program Bases Aerobic and Baduanjin Exercises in Post Stroke Elderly Patients Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06302946 on ClinicalTrials.gov ↗ ← All trials in Egypt