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Development of artificial hand for paralyzed patients

Phase 1
Conditions
Health Condition 1: G952- Other and unspecified cord compression
Registration Number
CTRI/2019/05/019054
Lead Sponsor
Canad India SCI Innovation award
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Cervical spinal cord injured individuals, 18 years of age or older , ASIA A, B, C

Have sustained a SCI for the preceding 6 months,

Ability to hold a 2.54-cm block of Box and Block apparatus with the thumb

Exclusion Criteria

Any co-morbidities with SCI such as head injury or any other injury affecting the the target hand (e.g. brachial plexus or peripheral nerve injuries)

have had trauma or surgery to the target hand or upper limb within the last 12 months

amputation of any digits on the target hand

not able to sit out of bed for at least two hours per day over three consecutive days

Any psychiatric illness diagnosed

Unstable patients

Contractures in targeted hand, spasticity more than grade 1 on modified ashworth scale

Study & Design

Study Type
BA/BE
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A soft robotic glove for hand functionality augmentation for tetraplegic patient. <br/ ><br> <br/ ><br>Initial functionality, based on what the control system would be developed is a grasping movement. <br/ ><br> <br/ ><br>In short, a wearable gloves, which will act as an external muscle, and help the patient fold his hand to grasp.Timepoint: o, 3 and 6 months assessment will be done using neurlogical scales.
Secondary Outcome Measures
NameTimeMethod
A soft robotic glove for hand functionality augmentation for tetraplegic patient. <br/ ><br> <br/ ><br>Initial functionality, based on what the control system would be developed is a grasping movement. <br/ ><br> <br/ ><br>In short, a wearable gloves, which will act as an external muscle, and help the patient fold his hand to grasp.Timepoint: The assessment will be done at 0,3 and 6 months period after the gloves are made. THe neurology and outcome measures will be compared.
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