Status:
UNKNOWN
Robotic Versus Conventional Therapy For Post-Stroke Hand Motoric Recovery
Lead Sponsor:
Hasanuddin University
Conditions:
Stroke
Physical Disability
Eligibility:
All Genders
20-85 years
Phase:
NA
Brief Summary
This clinical trial aims to compare the effectiveness of Robotic versus conventional mirror therapy among post-stroke patients. The main questions it aims to answer are: * Effectiveness of both inter...
Detailed Description
1. Research design This research is an experimental study with a randomized controlled trial research design. 2. Study Setting The research will be carried out among post-stroke patients at two teachi...
Eligibility Criteria
Inclusion
- Inclusion criteria:
- Patients aged 20 - 85 years.
- Non-haemorrhagic stroke/infarction with onset more than 3 months from the onset of the attack.
- Patients with unilateral upper limb hemiparesis.
- Modified Ashworth Scale (MAS) on fingers and hands \<3
- The patient has not undergone mirror therapy treatment before.
- Patients who are able to understand informed consent to participate in research.
- The patient had a Radiology imaging of the head at the time of stroke onset.
- Exclusion criteria:
- Patients with severe spasticity or contractures of the upper extremities.
- Patients with infarction/bleeding with extensive lesions covering 2 hemispheres.
- The patient has severe cognitive impairment that will interfere with the research objectives (MMSE score \>24).
- Patients post Digital Subtraction Angiography (DSA) procedures in the last 2 months.
- Patients with a history of seizures or epilepsy.
- Patients with visual field deficits or severe visual impairment.
- Patients who are unable to sit upright without assistance.
- Other uncontrolled medical conditions (musculoskeletal, neuromuscular, cardiorespiratory) that may interfere with the ability to exercise.
- Dropout criteria:
- Patients were excluded from the study if:
- Participant dies.
- Participants take part in the exercise \<3 times for 2 consecutive weeks.
- The participant refuses to continue the training session.
- Participants experience hemodynamic disorders during the training program phase.
- Participants experience neurological disorders during the training program phase.
Exclusion
Key Trial Info
Start Date :
December 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 30 2024
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT06155058
Start Date
December 1 2023
End Date
March 30 2024
Last Update
December 4 2023
Active Locations (3)
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1
Cerebellum Clinic
Makassar, South Sulawesi, Indonesia, 90231
2
Hasanuddin University, Faculty of Medicine
Makassar, South Sulawesi, Indonesia, 90245
3
Wahidin Sudirohusodo General Hospital
Makassar, South Sulawesi, Indonesia, 90245