Skip to main content
Clinical Trials/CTRI/2024/02/062762
CTRI/2024/02/062762
Not yet recruiting
未知

Effect of treadmill based gait training along with balance training on balance, gait and functional mobility among stroke patients. - nil

Vanshika Kalia0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: I630- Cerebral infarction due to thrombosis of precerebral arteries
Sponsor
Vanshika Kalia
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Vanshika Kalia

Eligibility Criteria

Inclusion Criteria

  • 1\.Diagnosis of Stroke: Participants must have a documented history of a stroke, confirmed by medical records and diagnostic imaging.
  • 2\.Age Range: Participants aged between 40\-60 years will be included to ensure a representative sample of stroke survivors within a manageable age range.
  • 3\.Time Since Stroke: Individuals who have experienced a stroke within the past 1 months to 2years will be eligible for inclusion, capturing a range of subacute to chronic stages of stroke recovery.
  • 4\.Ability to Ambulate: Individuals capable of walking with or without assistance, including assistive devices, will be considered for inclusion.
  • 5\.Cognitive Ability: Participants should possess sufficient cognitive ability to understand and follow instructions related to the rehabilitation program.
  • 6\. Willingness to participate: individuals who express a willingness and commitment to participate in the study.
  • 7\. Informed consent: individuals who provide informed written consent to participate in the study.

Exclusion Criteria

  • 1\.Unstable Medical Condition: Individuals with unstable medical conditions, such as uncontrolled hypertension, recent cardiac events, or severe respiratory disorders, will be excluded due to potential risks associated with physical exertion.
  • 2\.Severe Cognitive Impairment: Participants with severe cognitive impairments, as determined by standardized cognitive assessments, will be excluded, as they may not be able to actively engage in and benefit from the rehabilitation program.
  • 3\.Non\-ambulatory Individuals: Individuals who are completely non\-ambulatory and unable to walk, even with assistance, will be excluded from the study.
  • 4\.Language Barriers: Individuals who do not understand or speak the language of instruction used in the rehabilitation program and assessments will be excluded.
  • 5\.Unwillingness to Participate: Individuals unwilling or unable to provide informed consent, commit to the rehabilitation program, or attend scheduled sessions will be excluded.
  • 6\.Pregnancy: Pregnant individuals will be excluded due to potential risks associated with physical exertion and the intervention.
  • 7\.Uncontrolled Pain: Participants experiencing uncontrolled pain that could hinder their participation in the rehabilitation program will be excluded.

Outcomes

Primary Outcomes

Not specified

Similar Trials