NCT05590988Completed
Sensorimotor Arm Rehabilitation After Stroke
Sensorimotor Arm Rehabilitation After Stroke Using Tablet-based Bimanual Coordination Training
Source: ClinicalTrials.gov · Last updated 20 Apr 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 40 (actual)
- First submitted
- 13 Oct 2022
- Start date
- 7 Oct 2022
- Primary completion date
- 19 Aug 2024
- Lead sponsor
- BDH-Klinik Hessisch Oldendorf
- Diseases
- Stroke
- NCT number
- NCT05590988
What you commit to
- Study type: Interventional
- Participants enrolled: 40
- From 7 Oct 2022 to the primary completion date, 19 Aug 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- 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)
Other illness
- duration of illness \>3 months
Other
- Hemianopia and/or neglect
- pre-existing hemiparesis
- participation in another clinical trial within the last 30 days
- a pregnancy or breast-feeding period
Who the study is looking for
- 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)
Age in the registry: 36 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Institute for Neurorehabilitation Research, BDH-Clinic Hessich Oldendorf Coordinator of this site? Confirm its status | Hessisch Oldendorf | Germany | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.