Page 147 - Kaleidoscope Academic Conference Proceedings 2024
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Innovation and Digital Transformation for a Sustainable World




                                                              For  the  normal  population,  inclusion  criteria  consist  of
                                                              individuals of both genders aged above 18 with full active
                                                              range of motion (ROM) of the upper limb of the dominant
                                                              arm.  Exclusion  criteria  include  participants  with  ROM
                                                              restrictions of the wrist and hand, complaints of pain, injury,
                                                              fracture,  or  dislocation  in  the  dominant  arm,  and  those
                                                              unwilling to participate.

                                                              In  the  case  of  stroke  survivors,  inclusion  criteria  include
                                                              confirmation of stroke diagnosis by a clinician and MRI/CT
                                                              report, both genders aged above 18, and being in sub-acute
                                                              (3-26  weeks)  or  chronic  stage  (>12  months)  with  various
                                                              ranges  of  supination  and  pronation  of  the  forearm.
                                                              Additionally, participants should be able to sit independently
                                                              in  a  supported  chair.  Exclusion  criteria  encompass  other

                                                              neurological disorders and musculoskeletal disorders, a Mini
                                                              Mental  State  Examination  (MMSE)  score  <24,  visual
               Figure 3: CAD Model of Electronics Enclosure
                                                              impairments,  passive  restriction  of  ROM  of  the  wrist  and
                                                              hand, complaints of pain, injury, fracture, or dislocation in
                 3.  TESTING METHODOLOGY AND
                                                              the paretic arm, and unwillingness to participate.
                           IMPLEMENTATION
           The study has received approval from the Ethical Committee   4.  RESULTS AND DISCUSSION
           to conduct research. Participants from the normal population
           who  fulfill  the  inclusion  and  exclusion  criteria  will  be   Current guidelines suggest task-oriented training to enhance
                                                              drinking  skills,  but  determining  the  appropriate  dosage
           selected and provided with detailed explanations about the
           study. Each participant will receive an information sheet and   requires feedback on orientation magnitude.
           a consent form for approval before the study begins. Data
           will  be  sourced  from  stroke  rehabilitation  centers,   Dosage = Intensity × Frequency
           physiotherapy  OPDs,  and  neuro-physiotherapy  clinics  in
           Bangalore.                                         Our goal is to orient the glass vertically during the drinking
                                                              task to prevent spills. However, there are no standardized
                                                              scales to assess drinking task performance, and existing tools
                                                              do not provide real-time feedback on glass orientation.

                                                              4.1 Reliability Testing of Prototype and Validation with
                                                              KINOVEA Motion Analysis Tool

                                                              4.1.1   Reliability Testing

                                                              For  the  reliability  analysis  the  data  will  be  meticulously
                                                              collected on baseline characteristics such as age, gender, and
                                                              participation  level  of  the  subjects,  as  well  as  outcome
             Figure 4: Development Work flow of Proposed Device   measures. The intra-class correlation coefficient (ICC) will
                                                              be calculated between 10 different measurement trials.

                                                              Reliability  and  Concurrent  validity  testing  involved  two
                                                              phases such as;

                                                              Phase  1  consist  of  96  normal  individuals  to  establish  the
                                                              reliability of the tilt sensor device.

                                                              Phase 2 consist of 96 stroke survivors will be subdivided into
                                                              6 subgroups based on specific tilt orientation of  the glass
                                                              during activity.



                   Figure 5: Device attached to glass/mug







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