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Comparative analysis study on passive and active arm assistive devices for change of arm function in patients with spinal cord injury

Comparative analysis study on passive and active robotic devices to change arm functionality through proximal upper extremity assistance in patients with spinal cord injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007230
Enrollment
60
Registered
2022-04-26
Start date
2022-05-02
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

None listed

Interventions

Others(upper extremity orthosis) : 1. Randomly determine the order of WREX and Armon Ayura training, and apply the first equipment 3 times a week, 2 weeks each, for a total of 6 training sessions 2. A

Sponsors

National Rehabilitation Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Chronic patients more than 3 months after onset 2. Tetraplegia patients (C2-T1) 3. A patient with weakness in the muscle strength of the proximal part of the upper extremity. 4. If the proximal part of the upper extremity is good, endurance is low, and there is a limitation in performing daily activities such as eating and grooming. 5. Patients with shoulder and elbow range of motion of more than 90 degrees and 50 degrees, respectively. 6. Those who can sit tolerance for more than 30 minutes.

Exclusion criteria

Exclusion criteria: 1. Those with severe contracture problems in the upper extremities 2. Patients with obvious diseases that can cause muscle weakness due to abnormalities in the central nervous system other than spinal cord injury (eg, neuromyalgia) 3. Those who have difficulty following the therapist's instructions due to cognitive problems. 4. Those who have limited upper extremity movement due to stiffness of MAS 3 or higher 5. A person who can independently carry out daily life activities

Design outcomes

Primary

MeasureTime frame
Capabilities of upper extremity test(CUE-T);Quadriplegic Index of Funtional-Short Form(QIF-SF)

Secondary

MeasureTime frame
Manual muscle test(MMT);Range of motion(ROM);Upper extremity functional index(UEFI);Capabilities of upper extremity questionnaire(CUE-Q); Korean Quebec User Evaluation of satisfaction with Assistive Technology(K-QUEST);Individually Prioritised Problem Assessment(IPPA);Efficiency of Assistive Technology and Service(EATS-6D);Assessment of performance adaptability to equipment;pain and fatigue

Countries

Korea, Republic of

Contacts

Public ContactJung-Eun Lim

National Rehabilitation Center

lje276020@korea.kr+82-2-901-1345

Outcome results

None listed

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