TAB-APP: Sensorimotor Arm Rehabilitation After Stroke

Sponsor
BDH-Klinik Hessisch Oldendorf (Other)
Overall Status
Recruiting
CT.gov ID
NCT05590988
Collaborator
Gottfried Wilhelm Leibniz Universität Hannover (Other)
36
1
2
16.8
2.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Tablet-based training
  • Other: ergotherapeutic training
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Results are evaluated by an independent scientists and group assignment is pseudonymised.
Primary Purpose:
Basic Science
Official Title:
Sensorimotor Arm Rehabilitation After Stroke Using Tablet-based Bimanual Coordination Training
Actual Study Start Date :
Oct 7, 2022
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tablet

The intervention group trained bimanual coordination once a day for about 31 minutes on a total of ten days using a tablet game. A ball is to be moved on a circular line.

Other: Tablet-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.

Active Comparator: Aximo

The patients in the control group receive an ergotherapeutic therapy unit once a day for the same length of time (approx. 31 minutes) for a total of ten days, in which they train unilaterally. In this therapy unit, the control group uses the "Aximo". This is a comb stand and so-called "rolls" with which plugging tasks can be practiced. The patients should push the rolls into the stand fields with the affected hand. With the plug-in game, the patients can complete different tasks that challenge and train their hand-eye coordination, their fine motor skills and their ability to grasp things (e.g. following a specific pattern based on a template or putting colors in a specific order).

Other: ergotherapeutic 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.

Outcome Measures

Primary Outcome Measures

  1. 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.

  2. Changes in bimanual coordination 1 [Pre-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.

  3. Changes in bimanual coordination 2 [Pre-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 Outcome Measures

  1. Change of functional abilities [Pre-test (day 1), Post-test (day 18), Follow-Up (day 25)]

    measured by the difference of National Institutes of Health Stroke Scale (NIHSS)

  2. Change of activities of daily living [Pre-test (day 1), Post-test (day 18), Follow-Up (day 25)]

    measured by the difference of Barthel-Index (BI)

  3. Change of hand strength [Pre-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.

  4. Change of selective motor control after a stroke [Pre-test (day 1), Post-test (day 18), Follow-Up (day 25)]

    measured by the difference of the values of the "Fugl-Meyer-Test" (FMT)

Other Outcome Measures

  1. Change of functional connectivity of the motor system [Pre-test (day 1), Post-test (day 18)]

    measured by differences between resting state functional magnetic resonance imaging (fMRI) scans

Eligibility Criteria

Criteria

Ages Eligible for Study:
36 Years to 65 Years
Sexes Eligible for Study:
All
Accepts 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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institute for Neurorehabilitation Research, BDH-Clinic Hessich Oldendorf Hessisch Oldendorf Lower Saxony Germany 31840

Sponsors and Collaborators

  • BDH-Klinik Hessisch Oldendorf
  • Gottfried Wilhelm Leibniz Universität Hannover

Investigators

  • Principal Investigator: Jens D Rollnik, Prof. Dr., BDH-Klinik Hessich Oldendorf

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
BDH-Klinik Hessisch Oldendorf
ClinicalTrials.gov Identifier:
NCT05590988
Other Study ID Numbers:
  • TAB-APP
First Posted:
Oct 21, 2022
Last Update Posted:
Nov 7, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 7, 2022