Actively Recruiting

Phase Not Applicable
All Genders
NCT06563206

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

Led by Hasanuddin University · Updated on 2024-08-20

48

Participants Needed

2

Research Sites

73 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients after ischemic or hemorrhagic stroke
  • Stable hemodynamics and neurologic state
  • Patients who have never received treatment with any intervention
  • Able to watch television from 1 meter distance with or without glasses
  • Able to understand and provide informed consent to participate
Not Eligible

You will not qualify if you...

  • History of seizures or epilepsy
  • Severe cognitive disorders interfering with research (MMSE score <24)
  • Field deficits or severe vision disorders
  • Unable to sit upright without help
  • Significant pain in the affected upper limb
  • Significant sensory decreases in the affected upper limb
  • Uncontrolled medical conditions affecting musculoskeletal, neuromuscular, cardio-respiratory systems that risk exercise ability

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Hasanuddin University, Faculty of Medicine

Makassar, South Sulawesi, Indonesia, 90245

Actively Recruiting

2

Wahidin Sudirohusodo General Hospital

Makassar, South Sulawesi, Indonesia, 90245

Actively Recruiting

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Research Team

A

Auliyah Fadly, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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