Minimal Clinically Important Difference of Clinical Test of Sensory Interaction on Balance in Ind… (NCT06905730) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Minimal Clinically Important Difference of Clinical Test of Sensory Interaction on Balance in Individuals
Pakistan100 participantsStarted 2025-03-20
Plain-language summary
"Stroke is a major cause of disability worldwide, often leading to balance impairments due to deficits in sensory integration and motor control. These impairments hinder postural stability and functional independence, making balance rehabilitation a critical focus in sub-acute stroke care.
Who can participate
Age range18 Years – 85 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Type of stroke Participants must have experienced a first unilateral hemispheric supratentorial stroke, which may be either ischemic or hemorrhagic in nature.
* Only individuals who have been clinically diagnosed with a stroke within the past 3 to 6 months will be included.
* Participants must have a Functional Ambulation Classification (FAC) score of 3, indicating independent ambulation with supervision or the use of a walking aid.
* The individual must have sufficient cognitive and communication abilities to understand and follow instructions during assessments.
* The study will include patients in the early subacute phase of stroke recovery, defined as 7 days to 3 months post-onset.
* Participants must have a Montreal Cognitive Assessment (MoCA) score of at least 24, indicating normal cognitive function or only mild cognitive impairment
Exclusion Criteria:
* Individuals with severe cognitive impairments that prevent them from understanding, consenting to, or following simple instructions will be excluded.
* Participants with uncontrolled medical conditions such as cardiovascular disease or uncontrolled diabetes will not be eligible for the study.
* Individuals diagnosed with nerve compression conditions affecting motor or sensory function will be excluded.
* Patients exhibiting significant hemispatial neglect following a stroke will not be included in the study.
* Participants showing signs of unilateral spatial neglect, impacting their ability to …