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Tracking Balance and Walking Recovery in People After Stroke

Observes how sitting, standing and walking abilities recover in adults after stroke.

Plain-language title generated from the registry record
Registry title: Tracking Balance and Walking Recovery After Stroke

Key facts

Where
Sint-Pieters-Leeuw, BelgiumSee the site

Where in Belgium

  • Inkendaal rehabilitation hospitalSint-Pieters-Leeuw, BelgiumTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Vrije Universiteit Brussel
Trial code
NCT06806761
Record updated
16 July 2026
Original description
This study aims to understand how balance and walking abilities recover after a stroke, using innovative tools like an interactive assessment game. By observing patients over time, the investigators seek to identify recovery patterns that can improve rehabilitation strategies tailored to individual needs.Read full original descriptionShow less

Mapping the Time Course of Recovery of Sitting and Standing Balance and Walking After Stroke

This study aims to understand how balance and walking abilities recover after a stroke, using innovative tools like an interactive assessment game. By observing patients over time, the investigators seek to identify recovery patterns that can improve rehabilitation strategies tailored to individual needs.

Interacting with a game designed to assess balance and movement, participants will perform tasks involving sitting balance, standing balance, and gait initiation. The game measures aspects like reaction time, movement accuracy, and postural control, providing detailed insights into recovery progress. These data will validate prediction models to support personalized care.

The study is non-invasive, does not interfere with usual care, and prioritizes patient safety. The investigators' ultimate goal is to enhance the understanding of recovery, leading to better care and improved quality of life for stroke survivors.

Inclusion: Adult aged ≥18 years; Diagnosis of a supratentorial ischaemic or haemorrhagic stroke; Within the first eight weeks after stroke onset at the time of inclusion; Able to understand and perform the study procedures that are feasible at a given assessment time point, based on the advice of the treating therapist(s) and/or physician(s); Written informed consent provided by the participant or, where applicable, by a legally authorised representative.

Exclusion: Neurological or orthopaedic comorbidities unrelated to stroke that significantly impair motor function; Severe medical conditions that could compromise safety during the assessments; Major deficits in communication, memory or understanding that prevent participation in the study procedures; Insufficient comprehension of Dutch, French, German or English.

ClinicalTrials.gov NCT06806761