None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults aged between18 - 60 years. Healthy volunteers with no known musculoskeletal, neurological, or vascular pathology BMI between 18.5 and 25 kg/m to avoid excess fat affecting sensor readings Willing to provide informed consent No history of upper limb injury, surgery, or deformity.
Exclusion criteria
Exclusion criteria: Pregnant or lactating women Participants with metallic implants, pacemakers, or prosthetics in the upper limb Diagnosed with diabetes mellitus, neuropathy, Raynaud s disease, or vascular disorders Individuals with skin conditions or wounds at sensor application sites Participants with high anxiety or movement disorders preventing steady measurement Subjects who are currently undergoing any therapy (e.g., corticosteroids, physiotherapy) affecting circulation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Accuracy and reproducibility of upper limb Marma identification measured by positional deviation (mm), thermal asymmetry, impedance variation, and anatomical correlation via ultrasound.Timepoint: single study visit. | — |
Secondary
| Measure | Time frame |
|---|---|
| Thermal, bioelectric, vascular, and sensory variations at detected Marma sites compared with adjacent non-Marma areas.Timepoint: single study visit. | — |
Countries
India
Contacts
Parul Institute of Ayurved