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Recruiting NCT06641336

Perceptions of RehAtt Mixed Reality System

No phase Interventional Stroke

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: RehAtt.
Who it may be relevant to
Registry conditions: Stroke. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Slovenia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Perceptions of Using RehAtt Mixed Reality System in Stroke Motor Rehabilitation

Overview

The study aims to explore the patients' perspective on usability and feasibility of the RehAtt™ mixed-reality system during upper limb, gait and balance function rehabilitation.

Detailed description

Mixed reality is an immersive technology that can integrate virtual objects into the real world and adaptive scenarios. It offers the opportunity to train physical and cognitive aspects in stroke patients. The patients' perspectives were assessed with a semi-structured interview.

Interventions

  • Device RehAtt
    Each patient received the RehAtt intervention.

Primary outcome measures

  • Semi-structured interview [Time frame: On the day of the end of the intervention]

Eligibility criteria

Inclusion criteria

  • first ischaemic or hemorrhagic stroke,
  • one-sided hemiparesis,
  • adequate cognitive abilities.

Exclusion criteria

  • severe cognitive impairment,
  • aphasia,
  • known presence of an epileptic seizure in the last year,
  • other orthopaedic and neurological diseases affecting sensory or motor functions,
  • inability to sit independently,
  • severe visual impairment,
  • severe depression.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Device feasibility

Study locations

Slovenia · 1 center
  • University Rehabilitation Institute, Republic of Slovenia — Ljubljana

Identifiers

NCT: NCT06641336 · URIS202403

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗