The Effects of an Augmented Reality-Based Mirror Therapy System in Patients With Stroke

ConditionStroke
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMarmara University

About this trial

Objective The aim of this study is to investigate the effects of an augmented reality-based mirror therapy system (MirrARm), developed using sensor-based tracking and visual feedback principles, on upper extremity motor recovery and functional activity levels in patients with stroke.

Research Questions

This study seeks to address the following questions:

Does the MirrARm system improve upper extremity motor recovery and functional activity levels in patients with stroke?

Are the effects of the MirrARm system on upper extremity motor recovery and functional activity levels greater than those of conventional mirror therapy in patients with stroke?

Study Design and Comparison The MirrARm system will be compared with conventional mirror therapy to evaluate its effectiveness in patients with stroke.

Participants and Procedures Participants will take part in a treatment program administered three days per week for a total duration of eight weeks. Outcome measures will be assessed at baseline (Week 0), at mid-intervention (Week 4), and at the end of the intervention period (Week 8).

Eligibility criteria

Qualifiers

First-ever unilateral stroke diagnosed by a specialist physician,

Presence of post-stroke hemiplegia,

Age ≥ 18 years,

Time since stroke between 3 and 12 months,

Disqualifiers

Inability to sit independently in a supported chair,

Insufficient communication ability due to aphasia,

Presence of structural and/or acquired impairments limiting active movement of the unaffected upper limb,

Presence of visual or visual-perceptual impairments,

Trial design

Treatments tested in this trial

  • Augmented Reality-Based Mirror Therapy
  • Conventional Mirror Therapy
  • Conventional Physiotherapy Treatment

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Marmara University

Lead sponsor

Marmara University Scientific Research Projects Unit

Collaborator