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A Study to Test a New Arm Support Device (FxReach-KOOS) to Improve Arm Movement After Stroke

Design, Development, and Validation of a Kinematically Operated Orthosis for Synergy ( FxReach - KOOS) in Stroke Survivors - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/105011
Enrollment
30
Registered
2026-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: X- New Technology

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Dr M A Muhammad Easa
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Stroke diagnosis at least 6 months prior to commencement of study Healthy Individuals Passive range of motion in upper extremity joints within normal limits Fugl-Meyer Assessment- Upper Extremity- Elbow flexion- 2 , Elbow extension-1, Shoulder flexion-1 , Mass flexion- 2 , Mass extension- 0 Montreal Cognitive Assessment (MOCA) equal or lesser than 26 Adults aged 18 60 years

Exclusion criteria

Exclusion criteria: Open wounds or skin lesions on upper limb Anyother orthopedic,neurological and psychiatric comorbid conditions Excessive spasticity (Modified Ashworth Scale Lesser than 2) Recent botox injection to the affected limb (Lesser than 13 weeks)

Design outcomes

Primary

MeasureTime frame
To design and fabricate a device that assists elbow and finger extensionTimepoint: 8 weeks—

Secondary

MeasureTime frame
To evaluate the feasibility & usability of the device. To find the effect of FxReach- KOOS in stroke patients.Timepoint: 8 weeks—

Countries

India

Contacts

Public ContactDr Loganathan S

Sri Ramachandra Institute of Higher Education and Research (DU)

loganathanot@sriramachandra.edu.in9841958099

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026