NCT05581602Completed
Actimetry Monitoring of the Paretic Upper Limb in Chronic Post Stroke.
Actimeric Monitoring of the Use of the Paretic Upper Limb in the Activities of Daily Living of the Post-chronic Stroke Subject in a Home Environment
Source: ClinicalTrials.gov · Last updated 8 Oct 2026
Brief summary (registry, in English)
After a stroke, 80% of patients continue to have difficulty using their paretic upper limb in activities of daily living (ADL) despite post-stroke rehabilitation practices that aim to promote the use of the paretic upper limb. It is known that functional recovery depends on actual use (Use it or Loose it), but one-time measurements in the clinic do not allow quantification of the actual use of the paretic upper limb in daily life (in the person's living environment). The investigators hypothesize the feasibility of quantifying functional use of the paretic upper limb by actimetry in clinical routine.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 70 (actual)
- First submitted
- 11 Oct 2022
- Start date
- 13 Feb 2023
- Primary completion date
- 20 Sept 2025
- Lead sponsor
- University Hospital, Montpellier
- Diseases
- Stroke
- NCT number
- NCT05581602
What you commit to
- Study type: Interventional
- Participants enrolled: 70
- From 13 Feb 2023 to the primary completion date, 20 Sept 2025
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Pregnant or breastfeeding women
- Not eligible for inclusion, post-stroke subjects:
Other
- Non inclusion criteria common to all participants:
- Absence of free, informed and express oral consent
- No affiliation to a French social security system or beneficiary of such a system
- Patient protected by law
- Not understanding the constraints of the study
- Have cognitive impairments that prevent them from understanding the study
- With a known hemigligence in the medical record (omission \> 8 on bells test)
Who the study is looking for
- Be between 18 and 90 years old
- Post-stroke subjects should:
- Having a stroke with motor sequelae in the upper limb
- Be in the chronic phase (\>3 months post-stroke) of a stroke whatever the aetiology
Age in the registry: 18 years to 90 years · Sex: All · Accepts healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Hospital of Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Unknown status |
| Jerome FROGER Coordinator of this site? Confirm its status | Nîmes | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.