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Robotic-assisted Upper Extremity Training in Spinal Cord Injury Patients

Not Applicable
Completed
Conditions
Spinal Cord Injury Cervical
Interventions
Procedure: Conventional Rehabilitation
Procedure: Robotic REhabilitation
Registration Number
NCT03239301
Lead Sponsor
Ankara Physical Medicine and Rehabilitation Education and Research Hospital
Brief Summary

Study design: Controlled Trial Objective: To evaluate the effectiveness of robotic-assisted training of forearm and hand functions in spinal cord injury patients Setting: Ankara Physical Medicine and Rehabilitation Training and Research Hospital, Turkey Methods: Forty patients were allocated into robotic and control groups. Both groups received conventional rehabilitation program for four weeks. Moreover, robotic group received robotic rehabilitation program tailored to the patient five times a week (each session of 30 min).

Baseline data and post-intervention data was compared.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Ages between 18-50
  • Cervical Level of Spinal Cord Injury
Exclusion Criteria
  • Severe upper extremity contractures in the joints
  • Intensive spasticity (Ashworth 3-4)
  • Shoulder pain that causes exercise intolerance

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Robotic Rehabilitation + Conventional RehabRobotic REhabilitationThe Armeo Spring HocomAG Inc. (Volketswil, Switzerland) device was used in robot assisted upper limb rehabilitation program. A
Robotic Rehabilitation + Conventional RehabConventional RehabilitationThe Armeo Spring HocomAG Inc. (Volketswil, Switzerland) device was used in robot assisted upper limb rehabilitation program. A
Conventional RehabilitationConventional RehabilitationConventional rehabilitation program consisted range of motion (ROM) exercises, balance and coordination training, progressive resistive exercises, posture training, gait training, and occupational therapy as much as the patients tolerated. Conventional rehabilitation was tailored to the patient considering his requires and expectancies.
Primary Outcome Measures
NameTimeMethod
Spinal Cord Independence Measure IIIFour weeks

Scale Evaluating the Functionality and independence

Short Form-36Four weeks

Scale Evaluation the activities of daily living

Functional Independence MeasureFour weeks

Scale Evaluating the Functionality

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Ankara Physical MEdicine and REhabilitation Trainign and Research Hospital

🇹🇷

Ankara, Turkey

Ankara Fizik Tedavi ve REhabilitasyon Eğitim ve Araştırma Hastanesi

🇹🇷

Ankara, Turkey

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