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Multi-mode Stroke Rehabilitation System: Development and Validation of Clinical Efficacy

A Novel, Digital, and Interactive Multi-mode Stroke Rehabilitation System of Arm and Hand: Development and Validation of Clinical Efficacy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04441190
Enrollment
32
Registered
2020-06-22
Start date
2020-08-03
Completion date
2021-07-31
Last updated
2021-11-26

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

Conditions

Stroke, Cerebrovascular Disorders, Central Nervous System Diseases

Keywords

stroke, multi-mode rehabilitation, action observation, mirror therapy, digital image technology

Brief summary

The specific study aims will be: 1. To develop the novel, digital, and interactive MSR system of arm and hand with integrated digital action observation therapy (AOT) and mirror therapy (MT). 2. To pilot usability testing for examining the feasibility of this new MSR system from the users' experiences and feedback. 3. To examine the treatment effects of digital AOT, digital MT and a control intervention in patients with stroke by conducting a randomized controlled trial. 4. To identify who will be the possible good responders to digital AOT and MT based on their baseline motor function and mental imagery abilities.

Detailed description

Phase I: Multi-mode stroke rehabilitation (MSR) System Development & Usability Testing Ten patients with stroke and 4 certified occupational therapists were recruited in this phase I study. During the pilot testing, each stroke patient will try to use each training mode of digital AOT and MT by the assistance of the therapist. At the end of the pilot testing, the patients and the therapists will be asked to complete the System Usability Scale and a self-designed questionnaire to assess the user experience and perspective about this new MSR system and their view of its suitability for stroke patients. Phase II: Validation of Clinical Treatment Efficacy This three-arm, single-blind, randomized controlled trial will investigate the treatment effects among the 3 groups of digital AOT, digital MT, and dose-matched control intervention. An estimated 60 patients with stroke will be recruited to participate in this phase II study. Each participant will receive a total of 15 training sessions (60 minutes per session) for 3 to 4 weeks. Clinical outcome measures will be conducted at baseline, immediately after treatment (the fourth week), and at 1 month follow-up after treatment.

Interventions

BEHAVIORALDigital Action Observation Therapy (Digital AOT)

The participants will be asked to observe videos and then practice what the participants observed.

BEHAVIORALDigital Mirror Therapy (Digital MT)

The participants will observe the real-time self-recorded visual illusion, and move their upper limbs as could as possible.

The participants will receive upper-limb training without providing videos for observing neither providing them mirror illusions of movements.

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Phase I: Multi-mode stroke rehabilitation (MSR) System Development and Usability Testing For stroke patients Inclusion Criteria: * diagnosed as having a unilateral stroke; * aged from 20 to 80 years; * a baseline score of the Fugl-Meyer Assessment in a range of 20 to 60; * able to follow the instructions and able to provide user feedback verbally; * without aphasia and neglect For therapists Inclusion Criteria: * holding an occupational therapist license Phase II: Validation of Clinical Treatment Efficacy Inclusion Criteria: * diagnosed as having a unilateral stroke; * at least 6 months after stroke onset; * aged from 20 to 80 years; * a baseline score of FMA in a range of 20 to 60; * able to follow the study instructions; * capable of participating in therapy and assessment sessions

Exclusion criteria

* global or receptive aphasia, * severe neglect, * major medical problems or comorbidities that have influenced upper-limb usage or caused severe pain

Design outcomes

Primary

MeasureTime frameDescription
Change scores of Movement Imagery Questionnaire-Revised, Second Editionbaseline, 4 weeks, 2 monthsThe Movement Imagery Questionnaire-Revised, Second Edition is a 14-item questionnaire with sound reliability and validity to evaluate the ability of motion imagination in patients with stroke.
Change scores of Fugl-Meyer Assessmentbaseline, 4 weeks, 2 monthsThe upper-limb subsection of Fugl-Meyer Assessment is a measure with sound psychometric properties to evaluate motor impairments.

Secondary

MeasureTime frameDescription
Change scores of Revised Nottingham Sensory Assessmentbaseline, 4 weeks, 2 monthsThe Revised Nottingham Sensory Assessment is a standardized measure with good reliability to assess sensory function in patients with stroke.
Change scores of Barthel Indexbaseline, 4 weeks, 2 monthsThe Barthel Index is a validated tool designed to measure activities reflecting the daily living independence.
Change scores of Motor Activity Logbaseline, 4 weeks, 2 monthsThe Motor Activity Log is a semi-structured interview with good psychometric properties to assess the level of use of affected upper limb in 30 main activities of daily living.
Change scores of Chedoke Arm and Hand Activity Inventorybaseline, 4 weeks, 2 monthsThe Chedoke Arm and Hand Activity Inventory is a reliable and validated measure to assess the independence of stroke patients to perform activities of daily living with an affected upper limb.
Change scores of the visual analogue scale (VAS) of EQ-5D-5Lbaseline, 4 weeks, 2 monthsThe VAS of EQ-5D-5L scores will be scored from 0 to 100, with a higher score indicating better overall current health.
Change of joint angles of OPAL wearable sensorsbaseline, 4 weeks, 2 monthsThe OPAL wearable sensors is used to objectively record the movements of an affected upper limb in patients with stroke in real time, such as joint angles. Joint angles of the shoulder, elbow, and wrist will be calculated.
Change of joint velocity of OPAL wearable sensorsbaseline, 4 weeks, 2 monthsThe OPAL wearable sensors is used to objectively record the movements of an affected upper limb in patients with stroke in real time, such as joint velocity. The angular velocity of shoulder, elbow, and wrist will be also collected.
Change scores of the health state of EQ-5D-5Lbaseline, 4 weeks, 2 monthsThe questionnaire of EQ-5D-5L contains 5 dimensions, including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, and uses a 5-point Likert scale scored from 1 (no problem) to 5 (unable to/extreme problems); whereas, the numerical description of 5 dimensions represents the health state.
Change scores of Box and Block Testbaseline, 4 weeks, 2 monthsThe Box and Block Test is a tool with sound reliability and validity to evaluate hand dexterity of stroke patients.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026