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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06056219
Other study ID # B-ER-112-174
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 3, 2023
Est. completion date December 2024

Study information

Verified date October 2023
Source National Cheng-Kung University Hospital
Contact Hsiu-Yun Hsu, Ph.D
Phone 886-6-2353535
Email hyhsu@mail.ncku.edu.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In the proposed study, the investigators assumed that rhythmic-based training with immersive mirror visual feedback will provide a better treatment effects than traditional mirror therapy for the patients with unilateral stroke. The aim of the study is to examine the difference in the treatment effects among the combination of task-oriented training with either rhythmic-based training with immersive mirror visual feedback, or mirror therapy on the upper extremity function and brain activity of the stroke patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 36
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Clinical diagnosis of stroke with unilateral side involved; - A score of Mini-mental state examination greater than 24 for proving higher mental function - Time of onset > 6 months before treatment begins; and - Premorbid right-handedness. Exclusion Criteria: - Severe vision and hearing impairment; - Major cognitive-perceptual deficit; - Other brain disease.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Mirror therapy
30 minutes' mirror therapy included movements of forearm, wrist, fingers and thumb, as well as a tendon gliding exercise of less-affected upper extremity using a mirror box
Virtual reality-based mirror therapy with rhythmic skill training
30 minutes' virtual reality-based mirror therapy with rhythmic skill training included musical exercises involving virtual drums playing with less-affected upper extremity, and synchronized virtual drums playing and singing activity
Other:
Task-oriented training
20 minutes' motor training targeted to goals that are relevant to the functional needs of the patient

Locations

Country Name City State
Taiwan National Cheng-Kung University Hospital Tainan

Sponsors (1)

Lead Sponsor Collaborator
National Cheng-Kung University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Other functional Magnetic Resonance Imaging baseline, 9 weeks
Primary Change in the result of Fugl-Meyer assessment (FMA) for motor function of upper extremity test Each item is rated on a three-point ordinal scale (2 points for the detail being performed completely, 1 point for the detail being performed partially, and 0 for the detail not being performed). The motor performance score ranges from 0 to 66 for the upper extremity. baseline, 9 weeks and 21 weeks
Secondary Change in the result of Box and block test The score is the number of blocks carried from one box to the other in one minute. Higher values represent a better outcome. The minimum and maximum value is 0 and 150 respectively. baseline, 9 weeks and 21 weeks
Secondary Change in the result of Modified Ashworth scale (MAS) Muscle tone is defined by the resistance of a muscle being stretched without resistance. The MAS scores were distributed across the entire scale, ranging from 0 to 4, that is convenient for the clinician use. The grading of the scale is described as below: 0) no increase in muscle tone; 1) minimal resistance at the end of the range of motion (ROM); 1+) slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the reminder (less than half) of the ROM; 2) more marked increase in tone but only after part is easily flexed; 3) considerable increase in tone; and 4) passive movement is difficult and affected part is rigid in flexion or extension. baseline, 9 weeks and 21 weeks
Secondary Change in the result of Semmes-Weinstein monofilament (SWM) test The Semmes-Weinstein monofilament test examines the cutaneous pressure threshold, range from 1.65-6.65. Higher values represent a worse outcome baseline, 9 weeks and 21 weeks
Secondary Change in the result of Motor Activity Log Semi-structured interview examine how much and how well the subject uses their more-affected arm for 30 activities of daily living. Score range from 0-5. Higher values represent a better outcome baseline, 9 weeks and 21 weeks
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