Movement sonification in stroke rehabilitation

Movement sonification in stroke rehabilitation - SonReha

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00011419

Enrollment

Registered

2016-12-15

Start date

2017-09-08

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

I64

Interventions

Group 1: Movement therapy for upper extremity combined with movement sonification 3 weeks, 4 sessions per week, total of 12 sessions Group 2: Movement therapy for upper extremity with sham-acoustics

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: • unilateral ischemic or hemorraghic infarction (=4 weeks) • hemiparesis upper extremity (SULCS score =3)

Exclusion criteria

Exclusion criteria: • instabile or non strain proven fractures • patient is unable to sit • severe aphasia or severe cognitive impairment that makes study testing or therapy impossible

Design outcomes

Primary

Measure	Time frame
Box and Block Test By means of the Box and Block Test unilateral gross manual dexterity can be measured. The individual is instructed to move as many blocks as possible, one at a time, from one compartment of a box to the other. This test is sensitive to test therapy outcome and has a good to excellent reliabilty and validity. In addition the execution of this test is captured by a camera based movement analysis system (SIMI Motion) and kinematic parameters are analyzed. The primary outcome is measured 3 times: Before and after the specific study interventions, and after a 2 week follow-up period.	—

Measure

Time frame

Box and Block Test By means of the Box and Block Test unilateral gross manual dexterity can be measured. The individual is instructed to move as many blocks as possible, one at a time, from one compartment of a box to the other. This test is sensitive to test therapy outcome and has a good to excellent reliabilty and validity. In addition the execution of this test is captured by a camera based movement analysis system (SIMI Motion) and kinematic parameters are analyzed. The primary outcome is measured 3 times: Before and after the specific study interventions, and after a 2 week follow-up period.

—

Secondary

Measure	Time frame
Action-Research-Arm-Test (ARAT) and Stroke Upper Limbs Capacity Scale (SULCS) By means of the ARAT reach and grasp movements are measured. The ARAT is a 19 item measure divided into 4 sub-tests: grasp, grip, pinch, and gross arm movement. The SULCS is used to measure arm and hand function. It's a 10 item scale consiting of 3 items for arm function without hand function, 4 items for arm function and basic hand function, and 3 items for complex hand function. The secundary outcome parameters are testet at the same time points as the primary outcome. At baseline (before the Intervention phase) the Fugl-Meyer test for the upper extremities and the Montreal Cognitive Assessment (MOCA) are assessed.	—

Measure

Time frame

Action-Research-Arm-Test (ARAT) and Stroke Upper Limbs Capacity Scale (SULCS) By means of the ARAT reach and grasp movements are measured. The ARAT is a 19 item measure divided into 4 sub-tests: grasp, grip, pinch, and gross arm movement. The SULCS is used to measure arm and hand function. It's a 10 item scale consiting of 3 items for arm function without hand function, 4 items for arm function and basic hand function, and 3 items for complex hand function. The secundary outcome parameters are testet at the same time points as the primary outcome. At baseline (before the Intervention phase) the Fugl-Meyer test for the upper extremities and the Montreal Cognitive Assessment (MOCA) are assessed.

—

Countries

Germany

Contacts

Public ContactFriedemann Müller

Schön Klinik Bad Aibling

FMueller@schoen-kliniken.de08061 903 0

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 24, 2026