What is the trial like?
Participants in the TESCoN program faced mental and physical challenges, but many discovered new strength, resilience, and optimism along the way.
“TESCoN has been nothing but beneficial, both physically and mentally. Before TESCoN, I didn’t think I would gain any further improvements." – Participant
Approaching the program with openness and curiosity, several participants found the experience deeply rewarding:
“I went into the program with an open mind, not expecting anything magical, but I was really impressed. I enjoyed the experience, and the gains I made were definitely worth the investment.” – Participant
Physical progress was a common theme, as participants noticed significant improvements in mobility and strength:
“My arms are stronger, which means I can go further and faster in my wheelchair. I’m less fatigued. Before TESCoN, I needed a hoist for transfers. Now, I can transfer 50% of the time without a hoist.” - Participant
Despite the intensity of the program, TESCoN provided participants with the tools to regain independence, improve quality of life, and, above all, restore hope.
Is TESCoN Right for you?
The TESCoN program is designed for individuals with tetraplegia (quadriplegia) below the C4 level as a result of a traumatic spinal cord injury.
You may be eligible if:
- Your injury occurred 3-6 months ago, or over 12 months ago
- You are aged between 15 and 75 years
- You do not have any other neurological conditions
- You have not undergone upper limb tendon or nerve transfer surgery
What to Expect if You Participate
If you choose to participate in the TESCoN research study, your journey will begin with an initial screening, medical clearance, and assessments at the Royal Talbot Rehabilitation Centre.
Following the screening, you’ll attend therapy sessions Monday through Friday for 4 weeks, where you will receive TESCoN treatment alongside intensive physiotherapy for your arms and hands. Your progress will be assessed after the intervention and again three months later.
Time Commitment
- Assessments: Approximately 4-5 hours
- Therapy Sessions: 1-2 hours per session, five days a week for 4 weeks
Reimbursement
While you won’t be paid for participating, you will be reimbursed for reasonable expenses such as travel, parking, and refreshments during your time in the study.
Interested in joining the TESCoN Trial or learning more?
Contact: Dr. Maya Panisset, TESCoN Trial Coordinator
- maya.panisset@unimelb.edu.au
- Phone
- +61 405 027 127
- Address
- TESCoN Research Study, Room 1.272, Level 1, Royal Talbot Rehabilitation Hospital, Austin Health, KEW, VIC, 3101
The TESCoN trial is led by Professor Mary Galea. This project is funded by the Australian Medical Research Future Fund.
