Effect of Neuromuscular Stimulation and Mindfulness Exercise in Patients With Stroke
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: neuromuscular stimulation and mindfulness, neuromuscular electrical stimulation.
- Who it may be relevant to
- Registry conditions: Stroke. Basic parameters: 50 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effect of Neuromuscular Stimulation and Mindfulness Exercise on Pulmonary, Physical Functions and Stress in Patients With Stroke
Overview
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.
Detailed description
It is an interventional study in which 60 stroke patients will be 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. The experimental group participants will receive neuromuscular electrical stimulation that will last 12 consecutive weeks, three sessions per week protocol with Mindfulness.
Interventions
- Other neuromuscular stimulation and mindfulness
Receive neuromuscular stimulation and mindfulness breathing; the experimental group participants will receive neuromuscular electrical stimulation with Mindfulness. - Other neuromuscular electrical stimulation
participants in the control group perceived neuromuscular electrical stimulation
Primary outcome measures
- ventilatory function [Time frame: 12 weeks]
Secondary outcome measures (3)
- level of stress [Time frame: 12 weeks]
- Functional independence measure [Time frame: 12 weeks]
- level of physical function [Time frame: 12 weeks]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Faculty of Physical Therapy — Cairo
Identifiers
NCT: NCT06302946 · P.T.REC/012/005024