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Automatic Versus Intentional Movement Exercises to Enhance Arm Functions After Stroke

Automatic Versus Intentional Movement Exercises to Enhance Arm Functions After Stroke

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01565044
Acronym
AUTOTAB
Enrollment
26
Registered
2012-03-28
Start date
2012-09-27
Completion date
2017-11-03
Last updated
2025-12-19

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

Conditions

Stroke, Upper-limb Paresis

Keywords

Stroke, hemiplegia, automatic pilot, upper-limb rehabilitation

Brief summary

Many patients retain upper-limb motor impairment following stroke. Most conventional rehabilitation techniques are aimed to improve motor intentional movement by repeated exercises. These techniques require attentional load and are responsible for significant fatigue that probably represents a limiting factor. Alternatively, the automatic control of action is now well documented. A rehabilitation method based on this principle could allow recovery of more natural movements. Hypothesis: Stimulating automatic motricity improves upper-limb motor skills compared with a rehabilitation technique based on intentional movements.

Interventions

Subject will perform prehension exercises on an automated table. After the initiation of the arm movement, the target to be grasped is programmed to move in order to stimulate automatic motricity.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* All subjects must be between the ages of 18-80 and must not be pregnant * Patients volunteer to participate in the study, with a written informed consent signed * Affiliation to a national health insurance program * Hemiplegia after stroke * Stroke onset \>6 weeks and \<4 years prior to study enrollment * Patients able to perform the exercises on the automated table

Exclusion criteria

* Pregnancy * Excessive pain in any joint of the paretic extremity (VAS\>5) * Coexistent major neurological or psychiatric disease as to decrease number of confounders * Subjects with global aphasia and deficits of comprehension * Any substantial decrease in alertness, language reception, or attention that might interfere with understanding instructions for motor testing

Design outcomes

Primary

MeasureTime frameDescription
Fugl Meyer assessment (upper extremity) of motor recovery following stroke2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during this follow-up session (Day 26).

Secondary

MeasureTime frameDescription
modified Ashworth scaleimmediately following the last day of the intervention (Day 12) and 2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session.
Visual Analog Pain Scaleimmediately following the last day of the intervention (Day 12) and 2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session.
Box and block testimmediately following the last day of the intervention (Day 12) and 2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session
Fugl Meyer assessment (upper extremity) of motor recovery following strokeimmediately following the last day of the intervention (Day 12)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session
Motor Activity Log (MALimmediately following the last day of the intervention (Day 12) and 2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session.
Functional independence scale (MIF)immediately following the last day of the intervention (Day 12) and 2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session
Frenchey Arm Testimmediately following the last day of the intervention (Day 12) and 2 weeks following the last day of the intervention (Day 26)we are looking for a change in scores between the baseline session score (Day 1), and those collected during each follow-up session.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026