Stroke
Conditions
Brief summary
The goal of this study is to to examine whether rhythmic auditory stimulation improved movement speed, movement function of executing activities of daily living, and movement recovery of the affected upper limb, as well as quality of life in stroke patients. The main questions it aims to answer are: * Does rhythmic auditory stimulation improve movement speed in stroke patients? * Does rhythmic auditory stimulation improve movement function of executing activities of daily living in stroke patients? * Does rhythmic auditory stimulation improve movement recovery of the affected upper limb in stroke patients? * Does rhythmic auditory stimulation improve quality of life in stroke patients? Researchers will compare movement training with the aid of rhythmic auditory stimulation to movement training without the aid of rhythmic auditory stimulation to see if rhythmic auditory stimulation works to improve movement speed, movement function of executing activities of daily living, and movement recovery of the affected upper limb, as well as quality of life in stroke patients. Participants will: * Undergo movement tests and fill out questionnaires before and after the movement training program * Receive movement training for 40 minutes per session and three sessions per week for a total of 24 sessions
Interventions
BEHAVIORALrhythmic auditory stimulation incorporated in upper-limb movement training
Rhythmic auditory stimulation will be metronome beat sound with different tempi and will be incorporated in upper-limb movement training, which will last for 40 minutes per session, three sessions per week, and a total of 24 sessions.
BEHAVIORALUpper-limb movement training
Upper-limb movement training will last for 40 minutes per session, three sessions per week, and a total of 24 sessions.
Sponsors
Shu-Mei Wang
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* (1) Diagnosed with either ischaemic or hemorrhagic stroke, and a first-time occurrence; * (2) A unilateral stroke; * (3) The onset occurred six months or more prior to the experiment, indicating a chronic stage of stroke; * (4) The affected upper limb's proximal and distal joints are between Brunnstrom stages four to six, ensuring that the affected limb can execute the upper-limb functional movement training of this study; * (5) The affected upper limb's Modified Ashworth Scale score is ≤ 2, indicating no significant muscle stiffness (spasticity) in the affected limb; * (6) A Montreal Cognitive Assessment score of ≥ 24, ensuring comprehension of the instructions given during this study; * and (7) when we clap hands next to the affected ear of the participant who closes eyes, the participant is able to indicate the sound's source either verbally or through gestures, indicating no complete hearing loss in the affected ear and the ability to receive rhythmic auditory stimulation.
Exclusion criteria
* (1) Neurological diseases or medical conditions that affect upper-limb movements or hearing; * (2) Being participating in other experimental studies related to drug treatment or upper-limb movement therapy.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Nine-Hole Peg Test | Up to 1 week right before the 1st session of the intervention | A larger value (the recorded time for completing the task) means a slower movement. |
| Box and Block Test | Up to 1 week right before the 1st session of the intervention | A larger value (the number of blocks) means a faster movement. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Jebsen-Taylor Hand Function Test | Up to 1 week right before the 1st session of the intervention | A larger value (the time for completing the task) of each task means a slower movement. |
| the Fugl-Meyer Assessment | Up to 1 week right before the 1st session of the intervention | A higher value means better movement recovery. |
| the Stroke Impact Scale | Up to 1 week right before the 1st session of the intervention | A larger value means better quality of life. |
Countries
Taiwan
Outcome results
None listed