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NCT07682194Completed

Effects of Ecologically Valid VR Task-Oriented Exercises on Post-Stroke Motor and Cognitive Function

Effectiveness of Virtual Reality-based Task-oriented Exercises in Ecologically Valid Environments on Motor and Cognitive Function in Individuals Post-stroke. A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 2 Jul 2026

Brief summary (registry, in English)

Why is this study being done? After a stroke, many people have problems with movement, such as walking, balance, and using their arms and hands. They may also experience difficulties with thinking skills, including attention, memory, and problem-solving. These movement and thinking abilities work closely together during everyday activities, such as preparing a meal, shopping, or moving safely through the home. Traditional rehabilitation often treats movement and thinking problems separately. However, difficulties with attention, planning, and decision-making can affect a person's ability to move safely and learn new motor skills. Because of this, rehabilitation approaches that train both movement and thinking skills at the same time may provide greater benefits. Virtual reality (VR) technology can create realistic, interactive environments that allow people to practice everyday activities in a safe setting. However, there is limited research on VR programs that simultaneously challenge both movement and thinking skills, and little is known about whether any benefits last over time. What is the purpose of this study? The purpose of this study is to compare a virtual reality-based rehabilitation program that combines movement and cognitive training in realistic everyday environments with conventional occupational therapy. The study will evaluate whether the VR program leads to greater improvements in motor function and cognitive function after stroke and whether these improvements are maintained over the long term.

Status (registry)
Completed
Study type
Interventional
Enrollment
28 (actual)
First submitted
18 Jun 2026
Start date
16 Feb 2023
Primary completion date
9 Oct 2025
Lead sponsor
Hospitales Nisa
Diseases
Stroke
NCT number
NCT07682194

What you commit to

  • Study type: Interventional
  • Participants enrolled: 28
  • From 16 Feb 2023 to the primary completion date, 9 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Lower limb pain syndrome or peripheral nerve injury affecting the lower limbs.

Other

  • Severe visual or hearing deficits
  • Unilateral spatial neglect
  • Ataxia
  • Orthopedic abnormalities

Who the study is looking for

  • Diagnosis of stroke confirmed by computed tomography or magnetic resonance imaging
  • Chronicity \> six months
  • Ausence of severe cognitive deficits (Mini-Mental State Examination \> 23)
  • Ability to stand safely and without assistance
  • No or minimal muscle tone (Modified Ashworth Scale \< 3).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRENEA. Instituto de Rehabilitación Neurológica
Coordinator of this site? Confirm its status
ValenciaSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.