Health Condition 1: G988- Other disorders of nervous system
Conditions
Interventions
Intervention1: Cardiac Rehbilitation: A structured exercise-based cardiac rehabilitation program tailored to their respective needs and abilities will be administered. The program will aim to improve
Sponsors
Manav Rachna International Institute of Research & studies
Eligibility
Inclusion criteria
Inclusion criteria: The study will include patients who meet the following criteria: a confirmed diagnosis of ischemic stroke based on medical records and imaging studies, aged between 40 and 75 years, in the subacute stage of ischemic stroke according to the Burnstrom classification (1 to 3 months post-stroke), medically stable and cleared for exercise by a healthcare professional. Participants should also demonstrate willingness and ability to provide informed consent and possess adequate physical and cognitive abilities to engage in a structured rehabilitation program. Previous participation in a structured cardiac rehabilitation program will be an exclusion criterion.
Exclusion criteria
Exclusion criteria: Participants who exhibit severe cognitive impairments that hinder their ability to understand and participate in the study procedures will be excluded. Additionally, individuals with uncontrolled medical conditions that may interfere with exercise participation, such as severe cardiac or respiratory disease, uncontrolled hypertension, or active infections, will not be included in the study. Participants with contraindications to exercise as determined by a healthcare professional, such as recent myocardial infarction, unstable angina, severe arrhythmias, uncontrolled heart failure, or severe orthopedic conditions that prohibit safe exercise, will also be excluded. Those with significant neurological impairments that prevent safe and effective participation in the rehabilitation program, severe comorbidities, or conditions that limit the ability to engage in exercise safely will not be eligible for inclusion. Furthermore, pregnancy will be an exclusion criterion, as exercise prescription may need to be modified for pregnant individuals. Finally, individuals who are unable to provide informed consent or comply with the study procedures will not be included in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endurance, Functional strength & autonomic functionsTimepoint: Baseline & after 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Stroke specific quaity of lifeTimepoint: Baseline & after 3 months | — |
Countries
India
Contacts
Public ContactDr Moattar Raza Rizvi
Faculty of Allied Health Sciences
Outcome results
None listed