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NCT Number: NCT06302946

Effect of Neuromuscular Stimulation and Mindfulness Exercise in Patients With Stroke

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.

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Key information

Age range

50 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

neuromuscular stimulation and mindfulness

Other

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

Neuromuscular electrical stimulation

Other

participants in the control group perceived neuromuscular electrical stimulation

Primary outcomes

  1. ventilatory function

    Time frame: 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.

Secondary outcomes

  1. level of stress

    Time frame: 12 weeks

    perceived stress questionnaire Individual scores on the perceived stress questionnaire can range from 0 to 40 with higher scores indicating higher perceived tress

  2. Functional independence measure

    Time frame: 12 weeks

    The Functional independence measure consists of 18 measures organized into six dimensions and ranges from 18 to 126

  3. level of physical function

    Time frame: 12 weeks

    short physical performance battery group of measures that combines the results of the gait speed, chair stand and balance tests

Study contacts

Contact information is provided by the study sponsor or research team.

marwa elsayed, PhD

CONTACT

[email protected]

0201156033818

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Effect of Neuromuscular Stimulation and Mindfulness Exercise on Pulmonary, Physical Functions and Stress in Patients With Stroke

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Mar 12, 2024
Registry last updated
Mar 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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