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Development and testing of a orthosis for helping in rotation of palm for Spinal cord Injury patients

Development and trial of a pronation assist orthosis for SCI patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049205
Enrollment
10
Registered
2023-01-25
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: S141- Other and unspecified injuries ofcervical spinal cord

Interventions

Intervention1: questionnaire - OPUS upper extremity functional status (UEFS) and OPUS client satisfaction with device (CSD): OPUS questionnaire to fill with and without wearing orthosis on day 1 and d

Sponsors

AO spine Asia Pacific
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with C6-C7 level of injury, Patients with AIS- C, Patients with weak pronators (checked by MMT), Both male and female, Age between 18-60 years, Medically stable, No contractures in upper extremity, Patient sustained injury for at least 3 months

Exclusion criteria

Exclusion criteria: Patients with diabetes Patients with any psychiatric disorder Patients with any other neurological or orthopedic impairments in upper limb Pregnancy Malignancy Pacemaker Patients with any skin problems, any skin allergy  Medically unstable

Design outcomes

Primary

MeasureTime frame
Since most of the SCI patients have less power in the upper extremity, hence it is difficult for them to perform their ADL using the muscles to pronate the wrist position. With the help of this device the patient will be able to perform all their activities with assistance in pronation movement with the developed splint.Timepoint: Patient will be assessed after 4 weeks of using the orthosis

Secondary

MeasureTime frame
OPUS-CSD and OPUS-UEFS tool will be evaluate the patient satisfaction with the device and upper extremity functional status.Timepoint: 4 weeks

Countries

India

Contacts

Public ContactKomal chhikara

IIT Delhi

sehrawatkomal90@gmail.com9711987641

Outcome results

None listed

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