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Study identifier: NCT06986421 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Perception of Advanced Rehabilitation Technologies Among Post-Stroke Patients and Rehabilitation Staff

Condition: Post Stroke  ·  Sponsor: Hospices Civils de Lyon

PhaseN/A
Planned participants80
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This observational study aims to assess the perception of advanced rehabilitation technologies among three key groups involved in stroke recovery: post-stroke patients, physicians specialized in Physical and Rehabilitation Medicine, and allied health professionals. The study is conducted at HCL - Renée Sabran Hospital , specifically within the Kermes 2 department. Participants are selected using a non-probability sampling method, based on predefined inclusion and exclusion criteria. Data will be collected using a structured, author-developed questionnaire designed to evaluate attitudes, perceived usefulness, ease of use, and intention to adopt technologies such as exoskeletons, social robots, wearable interactive devices, and biofeedback systems. The questionnaire is applied at a single time point after obtaining informed consent. This research responds to the growing integration of technology in neurorehabilitation and seeks to identify potential barriers or facilitators to its adoption in clinical practice. The hypothesis is that there is a significant difference in perception and acceptance of advanced rehabilitation technologies between the three groups, influenced by their respective roles, experience, and level of exposure to such technologies.

This description comes directly from the study's public registry record.

Talk to the study team

David PLANTIER, Dr  ·  +33494381720  ·  david.plantier@chu-lyon.fr

Victor-Andrei Stan, Dr  ·  +33772151051  ·  victor-andrei.stan@drd.umfcd.ro

Always discuss trial participation with your own doctor first.

Locations (1)

HCL - Renée Sabran HospitalHyères, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06986421