Skip to main content
Clinical Trials/CTRI/2026/02/105024
CTRI/2026/02/105024RecruitingNot Applicable

Design, Development and Evaluation of Voluntary Motor Assessment System (VOMAS) for individuals with stroke

Gokul Krishnan S1 site in 1 country148 target enrollmentStarted: March 15, 2026Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
148
Locations
1
Primary Endpoint
To design and develop VOMAS, a sensor-integrated device

Study Overview

Brief Summary

This study focuses on the design, development, and evaluation of the Voluntary Motor Assessment System (VOMAS), a wearable sensor-based device created to objectively assess voluntary motor control in individuals with stroke. The device uses sensors placed on the shoulder, elbow, and wrist to measure joint movements during structured upper-limb tasks. It records quantitative parameters such as range of motion and movement control, and applies a standardized 7-point grading scale developed from existing motor control assessment frameworks. The study uses a cross-sectional diagnostic accuracy design, comparing VOMAS results with the Brunnstrom Stages of Motor Recovery. The goal is to provide a reliable, objective, and clinically useful tool to support occupational therapists in assessment and rehabilitation planning.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Participants must know either Tamil or English.
  • •This study will include both male and female participants.
  • •Participants aged between 18-
  • •The study will recruit both individuals with a clinical diagnosis of stroke and healthy participants Participants with a score of 26 and above on MOCA.

Exclusion Criteria

  • •Cognitive impairment Fixed joint contractures or deformities Visual or auditory impairment Other medical conditions, such as cardiovascular or respiratory illness.
  • •Recent orthopedic injury or surgery to the limbs or spine within the past 6 months Patients with Apraxia.

Outcomes

Primary Outcomes

To design and develop VOMAS, a sensor-integrated device

Time Frame: 8 weeks

To evaluate the sensitivity, specificity, and accuracy of VOMAS in identifying VMC impairment with the Brunnstrom Recovery Stages

Time Frame: 8 weeks

Secondary Outcomes

  • To evaluate the sensitivity, specificity, & accuracy of VOMAS in identifying VMC impairment with the Brunnstrom Recovery Stages

Investigators

Sponsor
Gokul Krishnan S
Sponsor Class
Other [Self Funding]
Responsible Party
Principal Investigator
Principal Investigator

Gokul Krishnan S

Sri Ramachandra Institute of Higher Education and research

Study Sites (1)

Loading locations...

Similar Trials