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Translation and Cultural Adaptation of the Erasmus Modified Nottingham Sensory Assessment Scale for the Lower Limb in Acquired Brain Injury Into French

Translation and Cultural Adaptation of the Erasmus Modified Nottingham Sensory Assessment Scale for the Lower Limb in Acquired Brain Injury Into French

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07613541
Acronym
F-EmNSA-MI
Enrollment
50
Registered
2026-05-29
Start date
2026-06-01
Completion date
2028-06-01
Last updated
2026-05-29

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

Conditions

Adults With Acquired Brain Injury

Keywords

Somatosensory deficits, Somesthesis, Somatosensory assessment, Stroke, Erasmus modified Nottingham Sensory Assessment, Somatosensation

Brief summary

There is a lack of validated and standardized tools in French for assessing somatosensory perception in adults with brain injuries. The only validated tool in French is the Fugl-Meyer Scale for Sensorimotor Recovery after a Stroke, which assesses only light touch sensitivity in two areas of the arm and leg, as well as proprioception for eight joints. The Erasmus Modified Nottingham Sensory Assessment (EmNSA) offers a detailed assessment of limb somatosensory perception in English. The upper limb (UL) version has been validated in French. The lower limb component remains to be translated and culturally adapted. This cross-cultural translation and adaptation project aims to validate this tool for a comprehensive clinical assessment of somatosensory deficits, applicable in both clinical practice and research. The project aims to validate the study of the metrological qualities (validity and reliability of the scale) of the French version of the EmNSA for the lower limbs.

Interventions

OTHERFrench Erasmus modified Nottingham Sensory Assessment scale

Clinical evaluation of somatosensation of the lower limbs in French

OTHERSelf-Reported Somatosensory Sensations questionnaire

Somatosensory sensation data

OTHERSensitive digital scale

Sensitive digital assessment data

Sponsors

University Hospital, Toulouse
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

* Patient with an acquired brain injury attested by brain imaging (CT scan or MRI) of more than seven days * Sufficient comprehension ability to participate in the study * Patients receiving care in the routine care pathway, as part of rehabilitation or functional assessments available for 6 weeks minimum and 12 weeks maximum * Ability to hold attention for at least 30 minutes * Aphasia Severity Scale score of 4 or higher * Anosognosia Assessment (from the Unilateral Neglect Assessment Battery) score of 1 or lower

Exclusion criteria

* Patient with peripheral neurological pathology * Severe communication disorders with a score of less than 4 on the Aphasia Severity Scale * Anosognosia Assessment (from the Unilateral Neglect Assessment Battery) score of 2 or higher * Major attention disorders making it impossible to take stock * Patient under guardianship

Design outcomes

Primary

MeasureTime frameDescription
Inter-rater reproducibilityDay 0 and day 7The intraclass correlation coefficient will be evaluated based on the results of the EmNSAMI measurements, obtained by 2 independent evaluators (E1 and E2 or E3; therapists with expertise in the evaluation of patients with acquired brain injury).

Countries

France

Contacts

CONTACTDavid GASQ, Professor
gasq.d@chu-toulouse.fr+33561777318

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 30, 2026