Myotonic Dystrophy type 1 (DM1) is a genetic multisystem disease causing muscle weakness and myotonia. As a result, upper limb function might become impaired. There are little research regarding rehabilitation and exercise for upper limb function in DM1. It is known from research on lower limb function in DM1 and other muscular dystrophies, that there are possibilities to improve function also in these deteriorating diseases. In this single subject experimental design study, 6-10 adults with DM1, who are at an inpatient rehabilitation center, will get intensive, but personally adapted senso- and robot assisted rehabilitation for arm- and hand function with Tyromotion Amadeo and Armeo Senso. These devices have previously been used in rehabilitation research for other neurological conditions. The participants will be followed up, and evaluated at a weekly basis, using video consultations. Fine motor skill dexterity test (9HPT) and the Nut and Bolt test will be used, and active range of motion (ROM) and muscle strenght and movement of upper limb will be measured. Furthermore, patient reported outcome measures (PROMS) on hand impairment and myotonia will be used, all with purpose to evaluate upper limb function.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
Robot assisted rehabilitation for arm- and hand function with Tyromotion Amadeo and Armeo Senso
Vikersund Rehabilitation Center
Vikersund, Akershus, Norway
Fine motor skill dexterity test, 9 hole peg test (9HPT)
Motor skill test
Time frame: 1-3 minutes
Range of motion (ROM)
Measure of ROM in upper limb joints
Time frame: 5-10 minutes
Nut and Bolt test
Motor skill test
Time frame: 5 minutes
Hand strength
Measured by Jamar digital dynamometer
Time frame: 5 minutes
Pinch Gauge
Finger strength measures by Jamar digital pinch gauge
Time frame: 5 minutes
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