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Muscle-Specific Multimodal AI for Sarcopenia Diagnosis

Development of Muscle-specific Multi-modal AI for Sarcopenia Diagnosis: Effects of Rehabilitation Training on Ant-muscle Aging

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07477574
Acronym
SARC-AI
Enrollment
75
Registered
2026-03-17
Start date
2026-03-01
Completion date
2028-02-28
Last updated
2026-03-17

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

Conditions

Sarcopenia

Keywords

Sarcopenia, Muscle aging, Multimodal AI, Muscle function

Brief summary

This study aims to develop a muscle-specific multimodal artificial intelligence (AI) model for the diagnosis of sarcopenia and to investigate the effects of rehabilitation training on muscle aging. Clinical, functional, and imaging data will be collected from participants with muscle function decline. Multimodal data, including muscle function measurements and clinical assessments, will be integrated to develop and validate an AI-based diagnostic model for sarcopenia. In addition, the effects of rehabilitation training on muscle function and muscle aging-related outcomes will be evaluated. The results of this study are expected to contribute to the development of digital biomarkers and precision rehabilitation strategies for sarcopenia.

Interventions

Participants will perform a structured rehabilitation training program designed to improve muscle strength, physical performance, and muscle function. Clinical assessments and muscle function measurements will be collected before and after the rehabilitation program to evaluate the effects of training and to support the development of a muscle-specific multimodal AI model for sarcopenia diagnosis.

Sponsors

Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 65 years or older * Individuals with reduced muscle function or at risk of sarcopenia * Able to participate in rehabilitation training * Able to understand the study procedures and provide written informed consent

Exclusion criteria

* Severe cardiovascular, neurological, or musculoskeletal conditions that limit participation in exercise * Severe cognitive impairment * Participation in other clinical trials that may influence study outcomes * Any medical condition judged by the investigator to make participation unsafe

Design outcomes

Primary

MeasureTime frameDescription
AI model performanceBaseline to 12 weeks after rehabilitation trainingThe performance of the muscle-specific multimodal artificial intelligence (AI) model for detecting sarcopenia will be evaluated using the Area Under the Receiver Operating Characteristic Curve (AUC). The AUC evaluates the ability of the AI model to discriminate between participants with and without sarcopenia(e.g., handgrip strength, gait speed, and appendicular skeletal muscle mass). The AUC value ranges from 0.5 to 1.0, where higher values indicate better discrimination performance of the AI model.

Secondary

MeasureTime frameDescription
Five-Times Chair Stand Test (5×STS)Baseline to 12 weeks after rehabilitation trainingTime required to complete the Five-Times Chair Stand Test, which assesses lower extremity muscle strength and functional performance. Participants will be instructed to stand up and sit down five times as quickly as possible with arms folded across the chest. The time required to complete the test will be recorded in seconds.
Gait SpeedBaseline to 12 weeks after rehabilitation trainingGait speed will be assessed using the 6-meter walk test. Participants will be instructed to walk at their usual pace over a 6-meter distance. Gait speed will be recorded in meters per second (m/s).
Appendicular Skeletal Muscle Mass (DEXA)Baseline to 12 weeks after rehabilitation trainingAppendicular skeletal muscle mass will be measured using Dual-energy X-ray Absorptiometry (DEXA). Muscle mass will be reported as appendicular lean mass (kg).
Appendicular Skeletal Muscle Mass (BIA)Baseline to 12 weeks after rehabilitation trainingAppendicular skeletal muscle mass will also be measured using Bioelectrical Impedance Analysis (BIA). Muscle mass will be reported as appendicular skeletal muscle mass (kg).
Sarcopenia ScreeningBaseline to 12 weeks after rehabilitation trainingSarcopenia risk will be assessed using the Strength, Assistance with walking, Rising from a chair, Climbing stairs, and Falls questionnaire (SARC-F). Scores range from 0 to 10, with higher scores indicating greater risk of sarcopenia.
Handgrip StrengthBaseline to 12 weeks after rehabilitation trainingHandgrip strength will be measured using a hand-held dynamometer. Maximum grip strength will be recorded in kilograms (kg).
Short Physical Performance Battery (SPPB)Time Frame: Baseline to 12 weeks after rehabilitation trainingPhysical performance will be assessed using the Short Physical Performance Battery (SPPB), which includes balance tests, gait speed, and the chair stand test. Total score ranges from 0 to 12, with higher scores indicating better physical performance.
Single Muscle Fiber Contractile PropertiesBaseline to 12 weeks after rehabilitation trainingContractile properties of permeabilized single muscle fibers will be assessed using a single muscle fiber mechanics system (Aurora Scientific, Canada). Measurements will include maximum isometric force (Po, mN), specific force (kN/m²), and rate of force redevelopment (ktr, s-¹) obtained from isolated muscle fibers. Higher values of maximum isometric force and specific force indicate greater muscle fiber contractile capacity.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026