Arm function training with visual and auditory feedback

interactive canetis biofeedback for training on upper extremity motor function in post-stroke subjects

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/12/016690

Enrollment

Registered

2018-12-17

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: G819- Hemiplegia, unspecified

Interventions

Intervention1: audio-visual biofeedback via interactive canetis biofeedback and bilateral self-aem exercise: forward reach outs- 100 lateral reach outs- 100 duration 45 mins Intervention2: audio-visua

Eligibility

Inclusion criteria

Inclusion criteria: - Subjects with age between 18 and above - Subjects can be male or female - MCA,PCA,ACA or IC Stroke - Both ischemic or hemorrhagic stroke - Subjects with left and right hemiplegic stroke - Subjects able to sit independently - Subjects with upper limb voluntary control grading 3-5 according to brunnstrom stages of recovery for upper limb - Subjects with average Montreal cognitive score > 26

Exclusion criteria

Exclusion criteria: - Subjects with the history of shoulder dislocation or fracture in upper limb - Subjects with VAS > 7 - Subjects with visual and hearing deficits - Medically unstable or ICU subjects - Subjects with previous history of stroke - Subjects with bilateral stroke - Subjects unwilling to participate

Design outcomes

Primary

Measure	Time frame
reaching performance scaleTimepoint: 0 day and 4 weeks	—

Secondary

Measure	Time frame
action reasearch arm test, fugl meyer scale for upper extrimityTimepoint: 0 day and 4 weeks	—

Countries

India

Contacts

Public ContactVENKATESAN R

OXFORD COLLEGE OF PHYSIOTHERAPY

k.sendil23@gmail.com8667701494

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026