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Evaluation on Standardized Circuits of the Interest of a Robotic Module of Assistance to the Driving 1 (SWADAPT1)

17. september 2026 oppdatert av: Pôle Saint Hélier

Evaluering av standardiserte kretsløp av interesse for en robotmodul for hjelp til kjøring av pasienter med nevrologiske lidelser, vanlige førere av elektriske rullestoler.

The device that is the subject of this investigation is a robotic assistance module for driving a semi-autonomous electric wheelchair. This module is designed to accessorize the electric wheelchair to improve the safety conditions when driving an electric wheelchair, thus reducing the wheelchair accident rate on the one hand and facilitating access to the wheelchair to persons who can not claim it without the use of a safety device of this type.

Studieoversikt

Detaljert beskrivelse

The device that is the subject of this investigation is a robotic assistance module for driving a semi-autonomous electric wheelchair. This module is designed to accessorize the electric wheelchair to improve the safety conditions when driving an electric wheelchair, thus reducing the wheelchair accident rate on the one hand and facilitating access to the wheelchair to persons who can not claim it without the use of a safety device of this type.

Each patient included will test a wheelchair equipped with a collision avoidance assistance module in 2 conditions, assistance activated or not. This evaluation will be carried out in 3 standardized test circuits of increasing difficulty, one week apart. At each session, the patient will perform the circuit 6 times, including 3 with activated assistance, in a random order established upstream.

Studietype

Intervensjonell

Registrering (Faktiske)

25

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Brittany Region
      • Rennes, Brittany Region, Frankrike, 35000
        • Pôle Saint-Hélier

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Aged over 18,
  • Having freely consented to participate in the study,
  • suffering from neurological disorders such as cerebro-lesion or neuro-degeneration,
  • Having benefited from a prescription of electric wheelchair and circulating in an electric wheelchair for more than 3 months,
  • of which the electric wheelchair is the main mode of transport,
  • The physical measurements (weight, height) are compatible with the use of the electric wheelchair chosen for the development of the robotics assistance module.

Exclusion Criteria:

  • Understanding difficulties preventing the realization of the protocol,
  • Motor disorders of the upper limb requiring additional driving technical assistance,
  • Patient having expressed difficulties impacting his safety of sedan and / or exterior.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Electric wheelchair with activated assistance module

This condition will be achieved in 3 standardized test circuits of increasing difficulty, one week apart. At each session, the patient will perform the circuit 6 times, including 3 with activated assistance, in a random order established upstream.

This evaluation will be carried out in 3 standardized test circuits of increasing difficulty, one week apart. At each session, the patient will perform the circuit 6 times, including 3 with activated assistance

Annen: Electric wheelchair with assistance module not activated

This condition will be achieved in 3 standardized test circuits of increasing difficulty, one week apart. At each session, the patient will perform the circuit 6 times, including 3 without activated assistance, in a random order established upstream.

This evaluation will be carried out in 3 standardized test circuits of increasing difficulty, one week apart. At each session, the patient will perform the circuit 6 times, including 3 with no activated assistance

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Number of collision
Tidsramme: Day 1

The primary judgment criterion is the number of collisions on different standardized circuits with and without activation of the robotic assistance module.

Day 1
Number of collision
Tidsramme: Day 8

The primary judgment criterion is the number of collisions on different standardized circuits with and without activation of the robotic assistance module.

Day 8
Number of collision
Tidsramme: Day 15

The primary judgment criterion is the number of collisions on different standardized circuits with and without activation of the robotic assistance module.

Day 15

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Driving Speed
Tidsramme: Day 1, Day 8 and Day 15

Speed measured by the completion time of the course with and without activation of the assistance system on the different circuits

Day 1, Day 8 and Day 15
Wheelchair Skill Test
Tidsramme: Day 1, Day 8 and Day 15

Driving performance measured by the Wheelchair Skill Test items corresponding to the different courses, with and without activation of the assistance system

Day 1, Day 8 and Day 15
NASA-Task Load Index
Tidsramme: Day 1, Day 8 and Day 15

The cognitive load of tests under both conditions will be measured by the NASA-Task Load Index. It is in the form of six scales where the participant must assign a score between zero and one hundred to each of them, score indicating a growing level of intensity. Three dimensions relate to the demands imposed on the subject (mental, physical and temporal demands) and three to the interaction of a subject with the task (effort, frustration and performance)

Day 1, Day 8 and Day 15
Ease of Use Questionnaire
Tidsramme: Day 1, Day 8 and Day 15

The satisfaction of the use of the electric wheelchair under the conditions will be evaluated by the self-questionnaire Ease of Use Questionnaire. It measures the subjective usability of a product or service. It is a 30-item survey that examines four dimensions of usability: usefulness, ease of use, ease of learning, and satisfaction. The questionnaires were constructed as seven-point Likert rating scales. Users were asked to rate agreement with the statements, ranging from strongly disagree (1) to strongly agree (7).

Day 1, Day 8 and Day 15
UTAUT (Unified theory of acceptance of technology) questionnaire
Tidsramme: Day 1, Day 8 and Day 15

Questionnaire of acceptability / acceptance of the tool and its use by patients based on the Unified Theory of Acceptance and Use Technology (UTAUT).

Day 1, Day 8 and Day 15

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Philippe Gallien, Doctor, Pôle Saint Hélier

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

3. juni 2019

Primær fullføring (Faktiske)

18. juni 2019

Studiet fullført (Faktiske)

18. juni 2019

Datoer for studieregistrering

Først innsendt

21. juni 2019

Først innsendt som oppfylte QC-kriteriene

27. august 2019

Først lagt ut (Faktiske)

28. august 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

21. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

17. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 2019-A00476-51

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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