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Predicting Real World Physical Activity and Upper Limb Use After Stroke

Profiling and Predicting the Natural Course of Real World Physical Activity and Upper Limb Use After Stroke

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03522519
Acronym
REUSE
Enrollment
98
Registered
2018-05-11
Start date
2018-09-01
Completion date
2021-03-31
Last updated
2021-11-29

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

Conditions

Stroke

Keywords

Physical Activity, Upper Extremity, Movement Sensors, Prognosis, Observational Cohort Study

Brief summary

Poststroke recovery mainly takes place within the first weeks to months and about 95% of the patients reach their maximum recovery 3 months after stroke onset. Poststroke rehabilitation is initiated as early as possible and aims to reduce functional consequences of stroke, allowing patients to integrate into the community. However, up to 75% of the patients remain disabled in the long term. Strikingly, about 20 to 30% of the patients show functional decline (i.e., learned-nonuse) in the long term - most often after having finished their intensive rehabilitation period - and even stroke survivors who have little or no residual disability are less physically active when compared to their age-matched peers. Poststroke outcomes can be well predicted early after stroke. However, the deficits early after stroke and the outcomes are measured by standardized clinical tests performed in the laboratory. The drawback of these tests is that they provide information about the best possible abilities of the patients, as they are encouraged by therapists in testing situations. This so called capacity does not necessarily reflect what patients do in daily life situations (i.e., performance or real world use). With the growing interest in the patients' performance, various assessments that objectively measure activities in daily life situations have been developed in the last few years. These devices capture movement in daily life situations in a sensitive and objective way. An additional benefit is that they are less hampered by floor or ceiling effects when compared to clinical laboratory measurements (i.e., clinimetrics). Nevertheless, outcome of real world performance is hardly ever used in clinical trials aiming to determine the effectiveness of stroke rehabilitation interventions. Actually, until today, the natural course of performance remains largely unknown, as are predictors for this course. It is also unknown to which extend patients' subjective reporting of performance matches objectively measured performance. Finally, although it is believed that there is a threshold for, for example, real life use of the paretic arm and further improvement, there is no evidence as to what this threshold is in terms of clinical laboratory measurements. The present prospective longitudinal cohort study fills in the gap regarding knowledge about the profile and predictability of two performance outcomes during the first year poststroke: engagement in physical activities and the use of the paretic upper limb. In addition, it will provide insight in how physical activity engagement and upper limb use measured by daily life assessments relate to standard clinical laboratory assessments. This knowledge is a prerequisite for the identification of patients' phenotypes and a first essential step towards the development of tailored (i.e., precision medicine), innovative rehabilitation interventions which enhance performance in terms of physical activities or upper limb use in daily life. The ultimate goal is to reduce poststroke disability and associated costs. RE-USE is a prospective longitudinal observational cohort study of 120 first-ever stroke patients, who will be assessed 3, 10, 28, 90 and 365 days after stroke onset, as well as at discharge of the rehabilitation center.

Interventions

BEHAVIORALReal world performance of physical activity and arm use

Patients will be assessed by using movement sensors and standard clinical assessments

Sponsors

University of Zurich
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

* First-ever ischemic or hemorrhagic stroke, confirmed by MRI-DWI and/or CT (recurrent strokes are allowed when already included in this study after a first-ever stroke) * Paresis or paralysis of the arm and/ or leg * Living independently before stroke (mRS \>2) * Age 18 years or older * Written informed consent of the patient or its legal representative after participants' information

Exclusion criteria

* Contra-indications on ethical grounds (vulnerable persons) * Neurological or other diseases affecting upper limb use and/ or physical activity before stroke * Known or suspected non-compliance, drug or alcohol abuse

Design outcomes

Primary

MeasureTime frameDescription
Daily life assessment of physical activity engagement and upper limb use90 days after stroke onsetReal world performance, measured with movement sensors (number)

Secondary

MeasureTime frameDescription
Upper limb motor function3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetFugl-Meyer Assessment (0-66 points, higher scores being better)
Motor function3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetMotricity Index (0-200 points, higher scores being better)
Trunk ability3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetTrunk Control Test (0-100 points, higher scores being better)
Sitting and standing balance10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetBerg Balance Scale (0-56 points, higher scores being better)
Walking ability (independence)3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetFunctional Ambulation Categories (0-5 points, higher scores being better)
Gait speed and cadence (time)10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetTen-Meter Walk Test
Upper limb capacity10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetAction Research Arm Test (0-56 points, higher scores being better)
Upper limb capacity dexterity10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetBox and Block Test (number of blocks)
Global disability3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetModified Rankin Scale (0-6 points, lower scores being better)
Fatigue10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetFatigue Severity Scale (9-63 point, lower scores being better)
Neurological impairments3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetNational Institutes of Health Stroke Scale (0-42 points, lower scores being better)
Neglect3 and 90 days after stroke onsetApples Test (number)
Patient-reported physical activity90 and 365 days after stroke onsetInternational Physical Activity Questionnaire (3 levels higher levels are better)
Patient-reported daily life upper limb use10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetMotor Activity Log - 14 item version (0-5 points, higher scores being better)
Patient-reported changes10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetGlobal Rating of Perceived Changes (1-7 points, higher scores being better; 1-10 points, lower scores being better)
Concomitant movement therapy3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetIntensity of therapy based on charts (minutes)
Serious Events and non-serious infections or cardiovascular events3, 10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetSerious Events (1. death; 2. life-threatening illness or injury; 3. in-patient or prolonged hospitalisation; 4. medical or surgical intervention to prevent life threatening illness; 5. led to fetal distress, death or a congenital abnormality or birth defect) and non-serious infections or cardiovascular events
Daily life assessment of physical activity engagement and upper limb use3, 10, 28 (expected rehabilitation discharge) and 365 days after stroke onsetReal world performance, measured with movement sensors (number)
Levels of anxiety and depression10, 28, 90 (expected rehabilitation discharge) and 365 days after stroke onsetHospital Anxiety and Depression Scale (0-42 points, higher scores indicate greater levels of anxiety or depression)
Health care costs and loss of income365 days after stroke onsetHealth care costs and loss of income in relation to the stroke (CHF)
Cognition3 and 90 days after stroke onsetMontreal Cognitive Assessment(0-30 points, higher scores being better)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026