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Recovery of Upper Limb Paresis at Discharge After Stroke and Its Level of Use in Activities of Daily Living 3 to 6 Months Later (Post AVC-AVQ)

NCT03118648 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 192

Last updated 2017-06-22

No results posted yet for this study

Summary

The aim is to reduct spontaneous use an activities of daily living of the paretic upper limb after stroke i six months after patient discharge from rehabilitation center. The level of functional recovery at rehabilitation discharge could better guide rehabilitation strategies to enhance independence and participation in daily life.

This study aims to determine, in patients after stroke, the optimal affected upper limb recovery threshold at rehabilitation discharge to predict spontaneous level of use of affected upper limb in activities of daily living, six month later.

This study is a multicentric prognostic prospective cohort study. The main prognostic variable will be the Action Arm Test (ARAT, Lyle, 1981) score at rehabilitation discharge and the predicted variable will be the Motor Activity Log - 28 (Taub et al. 1993) score at 6 months post discharge.

Conditions

  • Stroke Rehabilitation

Interventions

DIAGNOSTIC_TEST

Scale Action Research Arm Test (ARAT)

Measuring the functional recovery of the paretic upper limb rehabilitation outing with the scale ARAT

Sponsors & Collaborators

  • University Hospital, Bordeaux

    lead OTHER

Principal Investigators

  • Eric SORITA, PhD · University Hospital, Bordeaux

  • Paul PEREZ, MD · Unité de Soutien Méthodologique à la Recherche Clinique et Epidémiologique du CHU de Bordeaux

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-01
Primary Completion
2020-06-01
Completion
2020-06-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03118648 on ClinicalTrials.gov