Exploring how muscle properties affect arm function in stroke patients
The Relationship Between Upper Extremity Viscoelastic Properties and Functionality in Sub-acute Stroke Patients
This study is trying to see how the properties of arm muscles affect movement in stroke patients who had their first stroke a few months ago.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 50 Years |
| Sex | All |
| Sponsor | University of Gaziantep Academic / other |
| Locations | 1 site (Gaziantep, Sahinbey) |
| Trial ID | NCT05920837 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the relationship between the viscoelastic properties of upper extremity muscles and their functionality in individuals who have experienced a stroke. It utilizes the Box and Block Test to assess upper extremity function and the myotonPRO device to measure muscle properties such as tonus, stiffness, and elasticity. The study focuses on patients who had their first ischemic stroke 3-9 months prior and evaluates both sides of the body to gather comprehensive data on muscle performance and rehabilitation potential.
Who should consider this trial
Good fit: Ideal candidates are individuals who have experienced their first ischemic stroke 3-9 months ago with mild spasticity in the affected upper extremity.
Not a fit: Patients with cognitive deficits, other neurological or orthopedic diseases, or those experiencing pain from conditions like fibromyalgia may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance rehabilitation strategies for stroke patients, improving their independence and quality of life.
How similar studies have performed: While the specific approach of correlating viscoelastic properties with functionality in stroke patients may be novel, similar studies have shown that understanding muscle properties can significantly aid rehabilitation efforts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Patients who had ischemic SVO 3-9 months ago Individuals who have had a stroke for the first time MAS ≤ 2 of spasticity in paretic upper extremity Exclusion Criteria: TIA survivors Presence of cognitive deficits ( Mini-Mental State Examination score ≥ 24) Presence of another neurological, neuromuscular or orthopedic disease Presence of diseases that cause pain, such as fibromyalgia or arthritis Comorbidity with depression or psychiatric illness
Where this trial is running
Gaziantep, Sahinbey
- Tuba Maden — Gaziantep, Sahinbey, Turkey (Recruiting)
Study contacts
- Study coordinator: Tuba Maden, PhD
- Email: tuba.kmaden@gmail.com
- Phone: 05319340249
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.