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Measuring the Concurrent Validity of the Upper Limb Use Ratio With Accelerometers in an Ecological Situation After Stroke. (ValidFUR)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Enrolling

Conditions

Cerebrovascular Accident

Treatments

Behavioral: Objective assessment of upper limb use during activities in ecological situation

Study type

Interventional

Funder types

Other

Identifiers

NCT06509542
RECHMPL23_0428

Details and patient eligibility

About

The purpose of this stufy is to measure the concurrent validity of the upper limb use ratio with accelerometers in an ecological situation after stroke.

Full description

The first visit will be used to present the study and potential risks to patients, obtain their consent and collect clinical data. A second visit is planned for the patients who meet the eligibility requirements, to carry out activities in ecological situation.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject with hemiparesis following stroke
  • Subject participating in ecological activities during occupational therapy sessions
  • Adult subject aged 18 or over
  • Subject informed of study participation and not objecting to participation

Exclusion criteria

  • Other neurological or musculoskeletal disorders limiting use of upper limbs
  • Pregnant or breast-feeding woman,
  • Failure to obtain consent,
  • Non-affiliation with a social security scheme,
  • Persons under court protection,
  • Person protected by law (under guardianship or curatorship)
  • Participant in another research project with an exclusion period still ongoing.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Measure of FuncUseRatio using wrist-worn accelerometers and videos
Experimental group
Description:
The wristbands are made from hypoallergenic silicone and weigh 27 grams. They contain three accelerometers (AX3, Axivity, Newcastle Helix, United Kingdom), recording data in the three planes of space at a sampling frequency of 50 Hz and within an acceleration range of ±8 g. The wristbands will be worn on each wrist during the activities. Two high-definition video cameras, recording at least 50 images per second, will be positioned so that the movements of the patient's upper limbs are always visible. The location of the cameras will depend on the activity and the configuration of the room in which it takes place.
Treatment:
Behavioral: Objective assessment of upper limb use during activities in ecological situation

Trial contacts and locations

2

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Central trial contact

Karima Mrs. Bakhti, Dr

Data sourced from clinicaltrials.gov

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