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The Effect of Rehabilitative Games With SmartPose on Upper Extremity Recovery in Stroke Patients

I

Istanbul University - Cerrahpasa

Status

Completed

Conditions

Smartpose
Telerehabilitation
Stroke, Ischemic

Treatments

Other: Exercise
Other: SmartPose

Study type

Interventional

Funder types

Other

Identifiers

NCT06778525
Msc thesis

Details and patient eligibility

About

The goal of this clinical trial is to investigate the effects of SmartPose games on upper extremity motor, functional, and sensory recovery in patients with stroke. The main question it aims to answer is:

  • Does the use of rehabilitative games with the SmartPose application work to treat upper extremity motor, functional, and sensory recovery in stroke patients?

Researchers will compare the experimental group with the control group, which receives only conventional exercises with proven effectiveness, to determine whether SmartPose has an effect on upper extremity motor, functional, and sensory recovery in stroke patients.

The experimental group will receive 30 minutes of neuromuscular therapy and 30 minutes of SmartPose, 3 times a week for 8 weeks.

The control group will receive 60 minutes of neuromuscular therapy, 3 times a week for 8 weeks.

Enrollment

34 patients

Sex

All

Ages

35 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Mini Mental State Examination score ≥ 24
  • Age between 35 and 75 years
  • Medical condition sufficiently stable to allow participation in active rehabilitation
  • Brunnstrom Upper Extremity Stage ≥ 3
  • Minimum sixth week post-stroke
  • Ability to perform shoulder abduction and flexion against gravity with a minimum of 20°

Exclusion criteria

  • Presence of secondary impairments affecting upper extremity movement
  • Modified Ashworth Scale score of 4 or 5
  • Inability to maintain independent sitting balance
  • Visual impairment or loss that prevents the perception of visual materials

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

34 participants in 2 patient groups

Experimental Group
Experimental group
Description:
A one-hour exercise protocol will be administered in this group, consisting of 30 minutes of conventional exercises and 30 minutes of Smartpose exercises.
Treatment:
Other: SmartPose
Other: Exercise
Control
Active Comparator group
Description:
A one-hour conventional exercise program will be administered to this group.
Treatment:
Other: Exercise

Trial contacts and locations

1

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Central trial contact

Çilen Tavşanoğlu

Data sourced from clinicaltrials.gov

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