Hybrid Stroke Rehab With Mirror Priming
Hybrid Stroke Rehabilitation With Mirror Priming
1 other identifier
interventional
81
1 country
1
Brief Summary
This trial aims to examine the effects of enhanced mirror priming, overcoming the limitations of traditional mirror therapy, to achieve optimization and personalized intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable cardiovascular-diseases
Started Dec 2025
Longer than P75 for not_applicable cardiovascular-diseases
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 23, 2025
CompletedStudy Start
First participant enrolled
December 30, 2025
CompletedFirst Posted
Study publicly available on registry
January 7, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2030
January 7, 2026
December 1, 2025
5 years
December 23, 2025
December 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Fugl-Meyer Assessment
Baseline, 2 weeks, 4 weeks, 1 month, and 3 months post-intervention.
Secondary Outcomes (9)
Grip and pinch power
Baseline, 4 weeks, 1 month, and 3 months post-intervention.
Revised Nottingham Sensory Assessment
Baseline, 4 weeks, 1 month, and 3 months post-intervention.
Berg Balance Scale
Baseline, 4 weeks, 1 month, and 3 months post-intervention.
Montreal Cognitive Assessment
Baseline, 4 weeks, 1 month, and 3 months post-intervention.
Motor Activity Log
Baseline, 4 weeks, 1 month, and 3 months post-intervention.
- +4 more secondary outcomes
Study Arms (3)
High-dose enhanced mirror priming group
EXPERIMENTALLow-dose enhanced mirror priming group
EXPERIMENTALActive control group
ACTIVE COMPARATORInterventions
During the mirror priming process, the movement images of the participant's unaffected limb are mirrored to the affected side to provide visual feedback.
During conventional therapy, the participants typically receive interventions targeting the upper and lower limbs in addition to cognitive practice.
Eligibility Criteria
You may qualify if:
- A first-ever unilateral stroke ≥3 months
- Age between 20 and 80 years
- Baseline Fugl-Meyer Assessment Upper Extremity (FMA-UE) score \>10
- No severe spasticity in any joints of the affected arm
- Ability to follow the instructions
- No participation in other studies during the study period
- Willingness to provide informed written consent.
You may not qualify if:
- \. Serious medical problems or poor physical conditions that might be detrimental to study participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
E-Da Hospital
Kaohsiung City, Yanchao District, 82445, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Neuro-Rehabilitation Research Laboratory (NRRL)
Study Record Dates
First Submitted
December 23, 2025
First Posted
January 7, 2026
Study Start
December 30, 2025
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2030
Last Updated
January 7, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share