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Effect of Sarcopenia in Stroke Patients

Effect of Sarcopenia in Stroke Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05671705
Enrollment
83
Registered
2023-01-05
Start date
2023-01-02
Completion date
2024-12-27
Last updated
2025-06-11

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

Conditions

Stroke, Sarcopenia

Brief summary

Primary research purpose: -Prospective study to screen post stroke patients with sarcopenia and evaluate its effect on recovery Secondary research purpose: * To determine the degree of sarcopenia and correlation with poor functional prognosis of stroke in the stroke patient group. * To determine the degree of sarcopenia and correlation with dixon MRI of thigh muscle * To evaluate surface EMG (SEMG)-based signals and correlation with sarcopenia * To determine the degree of sarcopenia and correlation with brain morphometric changes

Detailed description

Patients with first-ever stroke will be enrolled and assessed for sarcopenia. The evaluation parameters will include standard sarcopenia parameters and also SEMG-based signals and imaging studies.

Interventions

DIAGNOSTIC_TESTDEXA Scan

Fu of diagnostic tests

Sponsors

Saint Vincent's Hospital, Korea
CollaboratorOTHER
The Catholic University of Korea
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients 65 years of age or older, stroke patients with first onset within 4 weeks

Exclusion criteria

* Patients who have not been evaluated for sarcopenia * Patients with neuromuscular diseases other than stroke that may affect gait function * Patients unable to conduct clinical trials according to instructions * Patients with uncontrolled medical/surgical disease * Patients with metal substances in the body such as cardiac pacemakers, cochlear implants, etc. * Patients who have difficulty collecting blood * Patients who are difficult to follow up after 6 months of onset due to moving to another area * Patients who have Parkinson's disease, dementia, or have a history of neuromuscular diseases such as Guillain-Barré syndrome or myasthenia gravis

Design outcomes

Primary

MeasureTime frameDescription
Change of Modified Rankin Scale6 months from the first onset of the strokeFunctional Disability -\> The scale runs from 0-6, running from perfect health without symptoms(0) to death(6).

Secondary

MeasureTime frameDescription
quadriceps muscle strengthwithin 4 weeks, 4 weeks, 8 weeks, 6 months from the first onset of the strokeLower extremity strength assessment:change in isometric quadriceps muscle strength (kg) from initial evaluation to the final evaluation
Fugl-Meyer motor scalewithin 4 weeks, 4 weeks, 8 weeks, 6 months from the first onset of the strokeMotor function assessment : Fugl-Meyer motor scale from initial evaluation to the final evaluation (Upper Extremity maximum score = 66; Lower Extremity maximum score = 34, Higher score means better outcome)
Functional Ambulation Categorywithin 4 weeks, 4 weeks, 8 weeks, 6 months from the first onset of the strokeGait function assessment : Functional Ambulation Category from initial evaluation to the final evaluation (Minimum 0, Maximum 5; Higher score means better outcome)
Berg balance scalewithin 4 weeks, 4 weeks, 8 weeks, 6 months from the first onset of the strokeBalance function: change in Berg balance scale from initial evaluation to the final evaluation (Minimum score 0, Maximum score 56, Higher score means better outcome)
Hand grip strengthwithin 4 weeks, 4 weeks, 8 weeks, 6 months from the first onset of the strokeGrip strength: Grip strength will be measured using a dynamometer
Thigh Dixon MRIwithin 4 weeks and 6 months from the first onset of the strokeMuscle quality : muscle circumference measured by the thigh MRI from initial evaluation to the final evaluation
Muscle ultrasonographywithin 4 weeks and 6 months from the first onset of the strokemuscle thickness(cm) measured by the ultrasound of the quadriceps muscle from initial evaluation to the final evaluation
serum biomarkers for sarcopeniawithin 4 weeks from the first onset of the strokeBNDF, IL-6
Digitalized SEMG signalswithin 4 weeks, 4 weeks, 8 weeks, 6 months from the first onset of the strokestate of the art EMG signals will be collected to assess muscle quality changes after stroke
Brain MRIwithin 4 weeks and 6 months from the first onset of the strokeBrain atrophy : change in the Global cortical atrophy scale(0-3) of the cerebral cortex from initial evaluation to the final evaluation

Countries

South Korea

Outcome results

None listed

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