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Measurement of Sarcopenia at Post-stroke Rehabilitation Outcome

Measurement of Sarcopenia at Post-stroke Rehabilitation Outcome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02793362
Enrollment
70
Registered
2016-06-08
Start date
2016-05-31
Completion date
2018-12-30
Last updated
2019-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Brief summary

The purposes of this study are 1. To explore effect of sarcopenia on recovery of post stroke hemiplegia 2. To explore the effect of stroke on sarcopenia and relationship between the degree of sarcopenia and respiration and swallowing function 3. To quantify and qualify post stroke loss of muscle mass 4. To validity the use of echointensity and elastography in evaluation of sarcopenia. By reaching the above list purposes, sarcopenia can be viewed as one of serious post stroke complications that is closely related to worth functional outcome, thereby emphasizing the importance of evaluation of sarcopenia as well as its prevention.

Detailed description

Sarcopenia occurs frequently among old population. The changes can rather occur earlier after trauma or generalized illness. However, the nature of these sarcopenia is different from that of geriatric population. Post stroke sarcopenia is underestimated however reduction in the motor uni number begins within 4 hours post stroke and after 3 weeks, sarcopenia can be seen in both hemiplegia and normal side. This muscular weakness can hinder functional recovery process.

Interventions

None listed

Sponsors

Bucheon St. Mary's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

for stroke patients * First ever subacute stroke patients whose lesions were confirmed in brain imaging (MRI/CT) * Patients who did not have difficulty in premorbid ambulation or activities of daily living. * Patients who can follow 1 step obey * Patients who can perform hand function test * Patients whose laboratory tests, neurologic, cognitive, and dysphagia evaluations are completed within 1 month from the onset date. * Patients who admitted/transferred into our department for at least 4 weeks, following conventional rehabilitation protocols. * Patients with at least 2 of MRS(Modified Ranking Score) and FAC(Functional ambulation category) scores.

Exclusion criteria

for stroke patients * Patients who do not meet the above listed criteria * Patients with double hemiplegia * Patients with other systemic diseases that can affect loss of muscle mass or causr malnutrition. (Example : chronic inflammatory disease, autoimmune disease, chronic intestinalis, active tuberculosis, immunocompromised state, AIDS, malignancy, pregnancy, amputation, or operation. * Patients with joint contracture who are difficult to perform sonographic evaluation. * Traumatic brain injury patients. Inclusion Criteria for normal subjects * Subjects who can walk independent without any difficult * Subjects without history of CNS or PNS lesion * MRS(Modified ranking scale) \<=2 * FAC(functional ambulation category) \>=2

Design outcomes

Primary

MeasureTime frame
Change in K-MBI score from initial evaluation to the final evaluation8 weeks, 12 weeks, 16 weeks from the first onset of the stroke

Secondary

MeasureTime frame
Change in Berg balance scale from initial evaluation to the final evaluation8 weeks, 12 weeks, 16 weeks from the first onset of the stroke
Change in Fatigue scale from initial evaluation to the final evaluation8 weeks, 12 weeks, 16 weeks from the first onset of the stroke
Change in Motricity index from initial evaluation to the final evaluation8 weeks, 12 weeks, 16 weeks from the first onset of the stroke
Change in Functional Oral Intake Scale (FOIS) from initial evaluation to the final evaluation8 weeks, 12 weeks, 16 weeks from the first onset of the stroke
Change in MMSE from initial evaluation to the final evaluation8 weeks, 12 weeks, 16 weeks from the first onset of the stroke

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026