Exergame and Robotic Therapy Impact on Tenascin-C and Functional Outcome on Stroke Patients

Recruiting now · Not applicable

Conditions studied: Stroke, Paralysis Arm

In brief

This clinical trial aims to compare the effectiveness of Robotic versus Exergame versus Standard therapy to improve hand function among post-stroke patients. The main questions it aims to answer are: 1, Effectiveness of interventions in functional outcome recovery across time 2. Effectiveness of interventions in affecting Tenascin-C level 3. Clinical outcome difference between all interventions Participants will be allocated into three groups, either a robotic group, exergame group as the main interventions, and standard rehabilitation group as the active comparator. A serial follow-up will be conducted to assess the selected clinical outcome and differences in outcome

Key facts

Study ID

NCT06563206

Run by

Hasanuddin University

People needed

48

Starts

2023-10-01

Expected to finish

2025-03-01

Last updated by the study team

2024-08-20

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients after ischemic or hemorrhagic stroke
• stable hemodynamics and neurologic state.
• Patients have never undergone treatment with any intervention
• Able to watch television with or without glasses from a distance of 1 meter.
• Patients can understand informed consent to participate in research

You may not qualify if…

• Patients with a history of seizures or epilepsy.
• Patients with severe cognitive disorders that can interfere with research objectives (MMSE score <24).
• Patients with field deficits or severe vision disorders.
• The patient is unable to sit upright without help.
• Patients with significant pain in the affected upper limb.
• Patients with significant sensory decreases in the upper limb that are affected
• Patients with other medical conditions (musculoskeletal, neuromuscular, cardio respiration) are uncontrolled and are at risk of disrupting the ability to exercise.
• Dropout Criteria
• Patients who were declared dead
• Refusing to continue the training session or less < 50% of all sessions.
• Experiencing hemodynamic and neurological disorders during the training program process.
• Experiencing cybersickness twice in successive training sessions

Where it is running

• Hasanuddin University, Faculty of Medicine — Makassar, South Sulawesi, Indonesia (enrolling)
• Wahidin Sudirohusodo General Hospital — Makassar, South Sulawesi, Indonesia (enrolling)

Full record on ClinicalTrials.gov

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