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StrokeRehAttNCT06641336

Perceptions of RehAtt Mixed Reality System

A study testing RehAtt in people with Stroke, run by University Rehabilitation Institute, Republic of Slovenia at 1 site in Slovenia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Stroke
What is being tested?
RehAtt
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteSlovenia
Study dates
11 Oct 2024to Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Metka Moharić, MD, PhD contact

+386 1 4758 441

metka.moharic@ir-rs.si

Slovenia1 site, 1 recruiting
  • University Rehabilitation Institute, Republic of Slovenia

    Ljubljana, 1000

    Nataša Bizovičar, MD, PhD, +386 1 4758351, natasa.bizovicar@ir-rs.si

    Recruiting

Other trials in Slovenia

About this study

Official title: Perceptions of Using RehAtt Mixed Reality System in Stroke Motor Rehabilitation

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.

Read the 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.

Conditions
Stroke
Being tested
RehAtt
Keywords
rehabilitation, mixed reality, motor rehabilitation, patients' perspective
Medical subject headings
Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • RehAttDevice

    Each patient received the RehAtt intervention.

Study groups in NCT06641336
Study groupRoleWhat they receive
RehAttExperimentalEach patient was included in the introduction session (performed by a psychologist), three sessions of occupational therapy and three sessions of physiotherapy. Each session lasted for 30 minutes. Occupational-therapy training was focused on activities aimed at improving upper limb function; physiotherapy training was focused on balance, walking and standing.
Receives: Device: RehAtt

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Semi-structured interview

    The interview was based on a questionnaire that included rating-scale-based questions on mixed-reality therapy meeting the patient's needs, frustration during the exercise, ease of use, difficulties encountered, motivational aspect, likability and usefulness of each exercise, and open-ended questions on motivation, overall view of the mixed-reality system and possible unwanted effects.

    Measured: On the day of the end of the intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Oct 2024
  2. Study start11 Oct 2024
  3. Primary completionOct 2026 (estimated)
  4. Study completionOct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Device feasibility
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
10 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06641336
Sponsor's protocol ID
URIS202403
Acronym
RehAtt
Status last verified
Jun 2026
First submitted
11 Oct 2024
Last updated
15 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing RehAtt in people with Stroke, run by University Rehabilitation Institute, Republic of Slovenia at 1 site in Slovenia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 15 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Slovenia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Metka Moharić, MD, PhD (+386 1 4758 441, metka.moharic@ir-rs.si), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Semi-structured interview (time frame: On the day of the end of the intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Jun 2026; AzTrials last refreshed its copy on 30 Oct 2026.

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