Post StrokeP-TECH-AVCNCT06986421
Perception of Advanced Rehabilitation Technologies Among Post-Stroke Patients and Rehabilitation Staff
An observational study of Post Stroke, run by Hospices Civils de Lyon at 1 site in France.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Post Stroke
- What is being tested?
- completion of a structured questionnaire
- How many people
- 80 participants
- Where
- 1 siteFrance
- Study dates
- 8 Jul 2025to 8 Jul 2026
- Phase
- Observational
- 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
- Adult, Older adult
Study population: Participants will be recruited from HCL - Renée Sabran Hospital, located in the PACA region (Provence-Alpes-Côte d'Azur), specifically from the Kermes 2 department, as well as through professional medical networks. The study population includes three main groups: (1) patients with a confirmed diagnosis of stroke, whether or not they have been exposed to advanced rehabilitation technologies; (2) physicians specialized in Physical and Rehabilitation Medicine involved in stroke management; and (3) allied health professionals (e.g., physiotherapists, psychologists, occupational therapists, speech therapists, neuropsychologists, psychomotor therapists) actively working in post-stroke rehabilitation settings. Recruitment will focus on individuals affiliated with institutions offering neurological rehabilitation services.
Who may be able to join
- Patients: Patients diagnosed with stroke, whether or not they have benefited from advanced rehabilitation technologies.
- Physicians: Physicians specialized in Physical and Rehabilitation Medicine who manage patients with stroke.
- Allied health professionals: Physiotherapists, psychologists, occupational therapists, speech therapists, neuropsychologists, and psychomotor therapists involved in the rehabilitation of post-stroke patients.
Who cannot join
- Refusal to participate in the study.
- Patients who do not wish to benefit from advanced rehabilitation technology.
- Healthcare professionals with no experience using advanced rehabilitation technologies.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site, 1 recruiting
- Recruiting
HCL - Renée Sabran Hospital
Hyères
Victor Andrei Stan, Dr, +33772151051, victor-andrei.stan@drd.umfcd.ro
victor-andrei STAN, Dr
About this study
Official title: Perception of Post-stroke Patients, Physical and Rehabilitation Medicine Physicians, and Allied Health Professionals Regarding Advanced Rehabilitation Technology
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.
- Conditions
- Post Stroke
- Being tested
- completion of a structured questionnaire
- Keywords
- Rehabilitation, Stroke, Advanced Technology, Perception, Questionnaire
- Medical subject headings
- Stroke
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
completion of a structured questionnaireOther
completion of a structured questionnaire
| Study group | Role | What they receive |
|---|---|---|
| Post-stroke patients | This group includes patients with a confirmed diagnosis of stroke, hospitalized or followed at HCL - Renée Sabran Hospital (Kermes 2 department), regardless of whether they have previously used advanced rehabilitation technologies. Receives: Other: completion of a structured questionnaire | |
| Physicians in Physical and Rehabilitation Medicine | This group consists of physicians specialized in Physical and Rehabilitation Medicine, actively involved in the treatment and rehabilitation of post-stroke patients. Recruited from HCL - Renée Sabran Hospital and affiliated professional networks Receives: Other: completion of a structured questionnaire | |
| Allied health professionals | This group includes allied health professionals involved in stroke rehabilitation, such as physiotherapists, occupational therapists, psychologists, speech therapists, neuropsychologists, and psychomotor therapists. All participants are affiliated with the HCL - Renée Sabran Hospital or collaborating institutions Receives: Other: completion of a structured questionnaire |
What is being measured
The primary outcome is the main question the study is designed to answer.
Perceptions of post-stroke patients, physical medicine and rehabilitation physicians and auxiliary medical staff on Advanced Rehabilitation Technologies.
The primary outcome measure evaluates the perception of advanced rehabilitation technologies among key stakeholders involved in post-stroke recovery. This perception is assessed using a structured questionnaire specifically developed by the authors, designed to capture attitudes, perceived usefulness, ease of use, and intention to adopt technologies such as exoskeletons, social robots, wearable interactive devices, and biofeedback systems. The instrument is applied to three target groups: post-stroke patients, physicians specializing in physical and rehabilitation medicine, and allied health professionals. This measure provides critical insights into the acceptability and potential integration of advanced technologies in neurorehabilitation practice.
Measured: Day 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 May 2025
- Study start8 Jul 2025
- Primary completion8 Jul 2026 (estimated)
- Study completion8 Jul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Post StrokeStudies of the same condition, open and under way.
- More trials run by Hospices Civils de LyonThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hospices Civils de Lyon
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- David PLANTIER, DR, Principal investigator, HCL
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06986421
- Sponsor's protocol ID
- 69HCL25_0378
- Other IDs
- 2025-A01110-49
- Acronym
- P-TECH-AVC
- Status last verified
- Jul 2025
- First submitted
- 15 May 2025
- Last updated
- 16 Jul 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Jul 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Perception of Post-stroke Patients, Physical and Rehabilitation Medicine Physicians, and Allied Health Professionals Regarding Advanced Rehabilitation Technology
- ClinicalTrials.gov ID
- NCT06986421
- Acronym / sponsor ID
- P-TECH-AVC / 69HCL25_0378
- Conditions
- Post Stroke
- Keywords
- Rehabilitation, Stroke, Advanced Technology, Perception, Questionnaire
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Hospices Civils de LyonUniversity, hospital or other
- Study start
- 8 Jul 2025 (actual)
- Primary completion
- 8 Jul 2026 (estimated)
- Study completion
- 8 Jul 2026 (estimated)
- First posted
- 23 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Post-stroke patients | – | Other: completion of a structured questionnaireThis group includes patients with a confirmed diagnosis of stroke, hospitalized or followed at HCL - Renée Sabran Hospital (Kermes 2 department), regardless of whether they have previously used advanced rehabilitation technologies. |
| Physicians in Physical and Rehabilitation Medicine | – | Other: completion of a structured questionnaireThis group consists of physicians specialized in Physical and Rehabilitation Medicine, actively involved in the treatment and rehabilitation of post-stroke patients. Recruited from HCL - Renée Sabran Hospital and affiliated professional networks |
| Allied health professionals | – | Other: completion of a structured questionnaireThis group includes allied health professionals involved in stroke rehabilitation, such as physiotherapists, occupational therapists, psychologists, speech therapists, neuropsychologists, and psychomotor therapists. All participants are affiliated with the HCL - Renée Sabran Hospital or collaborating institutions |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Participants will be recruited from HCL - Renée Sabran Hospital, located in the PACA region (Provence-Alpes-Côte d'Azur), specifically from the Kermes 2 department, as well as through professional medical networks. The study population includes three main groups: (1) patients with a confirmed diagnosis of stroke, whether or not they have been exposed to advanced rehabilitation technologies; (2) physicians specialized in Physical and Rehabilitation Medicine involved in stroke management; and (3) allied health professionals (e.g., physiotherapists, psychologists, occupational therapists, speech therapists, neuropsychologists, psychomotor therapists) actively working in post-stroke rehabilitation settings. Recruitment will focus on individuals affiliated with institutions offering neurological rehabilitation services.
Key inclusion criteria (3 listed)
- Patients: Patients diagnosed with stroke, whether or not they have benefited from advanced rehabilitation technologies.
- Physicians: Physicians specialized in Physical and Rehabilitation Medicine who manage patients with stroke.
- Allied health professionals: Physiotherapists, psychologists, occupational therapists, speech therapists, neuropsychologists, and psychomotor therapists involved in the rehabilitation of post-stroke patients.
Key exclusion criteria (3 listed)
- Refusal to participate in the study.
- Patients who do not wish to benefit from advanced rehabilitation technology.
- Healthcare professionals with no experience using advanced rehabilitation technologies.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| completion of a structured questionnairecompletion of a structured questionnaire | Other | Allied health professionals, Physicians in Physical and Rehabilitation Medicine, Post-stroke patients |
Primary outcome
Perceptions of post-stroke patients, physical medicine and rehabilitation physicians and auxiliary medical staff on Advanced Rehabilitation Technologies.
Time frame: Day 1
The primary outcome measure evaluates the perception of advanced rehabilitation technologies among key stakeholders involved in post-stroke recovery. This perception is assessed using a structured questionnaire specifically developed by the authors, designed to capture attitudes, perceived usefulness, ease of use, and intention to adopt technologies such as exoskeletons, social robots, wearable interactive devices, and biofeedback systems. The instrument is applied to three target groups: post-stroke patients, physicians specializing in physical and rehabilitation medicine, and allied health professionals. This measure provides critical insights into the acceptability and potential integration of advanced technologies in neurorehabilitation practice.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Jul 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
David PLANTIER, DR principal investigator
HCL
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Post Stroke, run by Hospices Civils de Lyon at 1 site in France.
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 3 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 16 Jul 2025. 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 France. 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 David PLANTIER, Dr (+33494381720, david.plantier@chu-lyon.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Perceptions of post-stroke patients, physical medicine and rehabilitation physicians and auxiliary medical staff on Advanced Rehabilitation Technologies. (time frame: Day 1). 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 16 Jul 2025.