None listed
Conditions
Brief summary
The project aims to evaluate the feasibility and clinical utility of the Tyromotion Diego robotic equipment to assist in the upper limb rehabilitation of people with a cervical spinal cord injury in acute care. A cervical spinal cord injury is catastrophic and causes significant functional limitations. Patients are often very keen to participate in rehabilitation sessions to assist them to undertake functional tasks such as self feeding, grooming or using a mobile phone. A six week intervention protocol involving pre and post outcome measures has been devised, including three sessions per week using the Tyromotion. We will investigate the outcomes achieved during the intervention period and interview patients about their experience of the intervention.
Interventions
Brief name: Use of Tyromotion Diego robotics Participants are consenting patients with a cervical level spinal cord injury who have been cleared by their consultant for the study, in acute care. Delivery of the protocol will be done by two occupational therapists and two researchers who have all been trained in the use of the Tyromotion Diego equipment. Procedure: 1. All patients with SCI are reviewed by OT when first admitted to the ward. At this stage, the OT will assess each patient to determine eligibility. If eligible, written consent for patient to participate to be provided by patient’s spinal rehabilitation consultant. 2. If eligible, the purpose and methodology of the trial will be discussed with the patient. The patient will then be provided with a participant information statement. Patient to provide informed written consent. 3. Patient assessed using the following assessments: - Canadian Occupational Performance Measure (COPM) - Spinal Cord Independence Measure (SCIM) - manual muscle testing of upper limb - goniometer range of motion (ROM) testing of upper limb - spasticity testing (Modified Ashworth Scale) - visual analogue pain scale - visual analogue fatigue scale - proprioception assessment - Tyromotion assessment of muscle strength and ROM. This will take approximately 2 x 1 hour sessions. 4. The Tyromotion Diego is a bi-lateral sling to support both upper limbs. Patients are seated in their wheelchairs and their arms are strapped in to the slings, and the robotics function removes gravity and allows assisted movement of the upper limbs in a number of directions. The Diego also records accurate ranges of motion at the shoulder and elbow, and the robotics function can be adjusted to provide less assistance as the patient progresses. 5. For the following 4.25 weeks, patient will have upper limb standard therapy and Tyromotion upper limb therapy timetabled. A diary will be kept with patient’s attendance noted, as well as activities participated in, exercises/games completed, functional tasks completed, number of repetitions and resistance settings/assistance provided. Standard upper limb therapy sessions will be scheduled for maximum 2 x 1 hour sessions per week (or up to patient’s tolerance). Sessions will be based on the patient’s functional goals and will be split with 30 minutes of upper limb exercises and 30 minutes application to functional tasks. - Tyromotion upper limb sessions will be scheduled for 3 x 1 hour sessions per week (1 hour per day in the AM). This will include 10 min set-up, 30 min of exercises with patient facing the computer screen. Games selected will be impairment oriented and games chosen specifically based on pathology. The patient will commence at the easiest level to allow the patient to master the game, then as the patient succeeds at each level, graded upwards in challenge. Exercises will focus on bilateral shoulder/elbow work. Time spent on each game will be recorded. The patient will then engage in 20 minutes of exercises facing away from Diego. This will include a function feeding/reach task which is bilateral task oriented. Time taken to complete tasks will be noted. Exercises will be selected based on the patient’s functional goals. The intervention will be delivered by an occupational therapist with experience in spinal cord injury management, face to face.
Sponsors
Study design
Eligibility
Inclusion criteria
1. Patients within the Royal North Shore Hospital Spinal Cord Injury Unit with a new acute complete or incomplete (ASIA impairment scale categories A-D) cervical spinal cord injury. 2. Involvement will be approved by the treating consultant. 3. Participants must provide informed consent. 4. Participant can tolerate sitting up in wheelchair for at least 1.5 hours. 5. Participant is over the age of 18 years old.
Exclusion criteria
1. Patient has a pre-existing spinal cord injury. 2. Spinal injury is lower than cervical level. 3. Consultant does not approve patient’s participation in study. (Aspects that may be considered by the consultant include but are not limited to , no active movement in upper limbs, medically unstable, delirium or acute confused state, shoulder subluxation, severe spasticity or spasms, shoulder and elbow contracture, unable to sit for 1.5 hours, epilepsy, severely visually impaired, poor balance or cerebral ataxia. 4. Participants will be removed from the study if they withdraw consent.