Skip to content

Stroke Patients' Preferences for an Exoskeleton for Lower Limb Rehabilitation Using the DCE Method (EXOPREF)

Stroke Patients' Preferences for an Exoskeleton for Lower Limb Rehabilitation Using the DCE Method.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06921031
Acronym
EXOPREF
Enrollment
60
Registered
2025-04-10
Start date
2025-01-15
Completion date
2025-12-31
Last updated
2025-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Stroke Patients

Brief summary

The main aim of this study is to investigate the preferences of individual stroke patients for key features of an exoskeleton, intended for lower limb rehabilitation, with a view to its potential integration into the design of future exoskeletons. This will be a multicenter study. Patients will be presented different scenarios of choices about the attributes about gait exoskeleton. Conditional logistic regression models will be used to define the preferences of the subjects.

Interventions

None listed

Sponsors

University Hospital, Brest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 years of age or older * informed consent to participate in the study * motor impairment secondary to stroke * ability to answer the questionnaire with or without assistance from a relative or interviewer

Exclusion criteria

\- history of lower-limb exoskeleton use

Design outcomes

Primary

MeasureTime frameDescription
Choices of the participantsOne hourThe study will describe the distribution of participants' choices among the scenarios presented in the experiment.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026