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Sensorimotor Arm Rehabilitation After Stroke

Sensorimotor Arm Rehabilitation After Stroke Using Tablet-based Bimanual Coordination Training

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05590988
Acronym
TAB-APP
Enrollment
40
Registered
2022-10-21
Start date
2022-10-07
Completion date
2026-03-15
Last updated
2026-04-20

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

Conditions

Hemiparesis, Stroke

Brief summary

Hemiparesis is a frequently observed symptom of stroke. There are various therapy options that are used in the rehabilitation of patients. Some studies have shown that, in addition to unilateral arm training, bilateral arm training can also lead to positive results in treatment and is a useful addition to therapy. The newly developed app requires the coordination of both arms in certain time sequences and intensities or rhythms and addresses different sensory modalities (visual, auditory and kinesthetic). The aim of the study is to examine whether tablet-based training improves bimanual coordination.

Interventions

OTHERTablet-based training

Each task is performed for one minute, followed by a 2-minute break. After the task has been performed three times, there is a 5-minute break. The training block is then carried out twice more. This means that three "blocks" are carried out for each therapy unit.

OTHERergotherapeutic training

A task is performed for one minute at a time, followed by a 2-minute break. Once three rounds have been completed, there is a 5-minute break. As in the intervention group, there are a total of three training blocks.

Sponsors

BDH-Klinik Hessisch Oldendorf
Lead SponsorOTHER
Gottfried Wilhelm Leibniz Universität Hannover
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

Results are evaluated by an independent scientists and group assignment is pseudonymised.

Eligibility

Sex/Gender
ALL
Age
36 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of an ischemic/hemorrhagic stroke * moderate upper extremity paresis: 30 to 60 cubes in the Box-and-Block Test (BBT) * sufficient resilience / alertness (active participation possible for at least 30 minutes) * ability to give consent (written declaration of consent from the patient)

Exclusion criteria

* Hemianopia and/or neglect * duration of illness \>3 months * pre-existing hemiparesis * participation in another clinical trial within the last 30 days * a pregnancy or breast-feeding period * contraindications for MRI: claustrophobia; metallic or magnetic implants that contain iron, cobalt or nickel (e.g. pacemakers, brain pacemakers, automatic insulin pumps, electrodes, plates, clips, implanted hearing aids, dental implants, metal endoprostheses, metal parts or metal splinters in the body)

Design outcomes

Primary

MeasureTime frameDescription
Change of the hand/arm motor skills (unilateral)Pre-test (day 1), Post-test (day 18), Follow-Up (day 25)measured by the difference in moving wooden cubes in the Box-and-Block Test (BBT) The BBT measures unilateral gross manual dexterity. The patient has to move as many individual cubes as possible from one side of the box over a partition to the other within one minute. The test takes place in a seated position and is performed sequentially with the non-impaired hand and the affected hand. The number of cubes transported for each side is evaluated.
Changes in bimanual coordination 1Pre-test (day 1), Post-test (day 18), Follow-Up (day 25)measured by the difference in moving wooden cubes in the modified Box-and-Block Test (mBBT) For this, a modified box with three compartments and two partitions is used. The task is to take a cube in one hand, pass it to the other hand over the first partition and then transport it over the second partition to the outer compartment. The dice are then counted in the outer compartment. The dice that fall from one hand to the other in the middle compartment are counted separately. The task is performed twice, starting with the unimpaired hand in the first run and with the impaired hand in the second run. The subject has one minute per round to transport as many cubes as possible to the outer compartment.
Changes in bimanual coordination 2Pre-test (day 1), Post-test (day 18), Follow-Up (day 25)measured by the difference in activity index (calculated from acceleration, movement amplitude and movement frequency during the use of the tablet game)

Secondary

MeasureTime frameDescription
Change of functional abilitiesPre-test (day 1), Post-test (day 18), Follow-Up (day 25)measured by the difference of National Institutes of Health Stroke Scale (NIHSS)
Change of activities of daily livingPre-test (day 1), Post-test (day 18), Follow-Up (day 25)measured by the difference of Barthel-Index (BI)
Change of hand strengthPre-test (day 1), Post-test (day 18), Follow-Up (day 25)Hand strength is measured with a KERN MAP digital hand force gauge. The change of strength (in kg) is calculated.
Change of selective motor control after a strokePre-test (day 1), Post-test (day 18), Follow-Up (day 25)measured by the difference of the values of the "Fugl-Meyer-Test" (FMT)

Countries

Germany

Contacts

PRINCIPAL_INVESTIGATORJens D Rollnik, Prof. Dr.

BDH-Klinik Hessich Oldendorf

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 21, 2026