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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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    Page 1 of 1 (3 locations)

    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