Effect of a Semiotically-Optimized Video Education Model on Post-Stroke Rehabilitation
SOVE-Stroke
A Randomized Controlled Trial Evaluating the Effect of a Semiotically-Optimized Video Education Model on Activities of Daily Living, Sleep Quality, Anxiety, Depression, and Patient Satisfaction in Post-Stroke Rehabilitation Patients
3 other identifiers
interventional
200
1 country
1
Brief Summary
Stroke is a leading cause of death and disability worldwide. Many stroke survivors face difficulties with daily activities, sleep problems, anxiety, and depression during recovery. Health education videos can help patients learn about rehabilitation, but standard videos often contain too much information and are hard for patients to follow. This study aims to test whether using semiotics - the science of signs and symbols - to redesign health education videos can help stroke patients better comprehend and apply rehabilitation instructions. The study is designed to include 200 stroke patients at Siping Central Hospital in Jilin Province, China. Patients will be randomly assigned to either the semiotic-optimized video group or the standard health education video group. Outcome measures, including activities of daily living, sleep quality, anxiety, depression, and satisfaction with care, will be assessed before and after the intervention to evaluate the effectiveness of the optimized video education model.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2023
CompletedFirst Submitted
Initial submission to the registry
July 8, 2026
CompletedFirst Posted
Study publicly available on registry
July 17, 2026
CompletedJuly 17, 2026
July 1, 2026
12 months
July 8, 2026
July 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Activities of Daily Living (ADL)
Modified Barthel Index (MBI), The MBI comprises 10 items assessing ADL, with a total score ranging from 0 to 100. Higher scores indicate better independence in daily living activities.
Baseline and Day 28
Secondary Outcomes (4)
Change in Sleep Quality
Baseline and Day 28
Change in Anxiety
Baseline and Day 28
Change in Depression
Baseline and Day 28
Patient Satisfaction
Day 28
Study Arms (2)
Experimental: Semiotically-Optimized Video Group
EXPERIMENTALParticipants received semiotically-optimized video-based health education, 28 days, twice daily, 5-8 minutes per session, including music and video feedback.
Active Comparator: Standard Video Group
ACTIVE COMPARATORParticipants received standard video-based health education, 28 days, routine rehabilitation instructional videos and assistive device guidance.
Interventions
Participants received semiotically-optimized video-based health education, 28 days, twice daily, 5-8 minutes per session, including music and video feedback.
Participants received standard video-based health education, 28 days, routine rehabilitation instructional videos and assistive device guidance.
Eligibility Criteria
You may qualify if:
- Imaging-confirmed cerebral infarction per 2019 Chinese Guidelines
- Age ≥18 years
- Stable condition during rehabilitation phase
- Alert, able to comprehend and operate video playback
- Signed informed consent
You may not qualify if:
- Incomplete records, inaccurate data, or failure to complete the intervention
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Siping Central People's Hospital
Siping, Jilin, 136000, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yang Liu, PhD
Xiamen University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
July 8, 2026
First Posted
July 17, 2026
Study Start
January 1, 2023
Primary Completion
December 31, 2023
Study Completion
December 31, 2023
Last Updated
July 17, 2026
Record last verified: 2026-07