Development and Application of Intelligent Assessment System of Longshi Scale
NCT ID: NCT05214638
Last Updated: 2022-01-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
115 participants
OBSERVATIONAL
2021-09-10
2021-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Assessed with the paper version of Longshi Scale first and then with electronic version
No interventions assigned to this group
Assessed with the electronic version of Longshi Scale first and then with the paper version
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age≥18 years
* diagnosis of cerebral infraction or intracerebral hemorrhage
* stable vital signs
* willingness to participate in the study with informed consent
2. Professional evaluators:
* One to ten years of working experience
* experience in rehabilitation scientific research or education related work for more than two years
* association with Longshi Scale research
3. Non-professional evaluators：
* the family or caregiver of stroke survivors
* ability to read and communicate
* willingness to participate in the study with informed consent
Exclusion Criteria
* brain tumor, Parkinson's disease or active epilepsy within past three months
* impaired cognitive functions
* participation in any other clinical study
2. Professional evaluators:
* refusal to participate in the study
3. Non-professional evaluators:
* care for patients with serious mental health problems
* refusal to participate in the study
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Shenzhen Second People's Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Shenzhen Second People's Hospital
Shenzhen, Guangdong, China
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Xue K, Li W, Liu F, Liu X, Wong J, Zhou M, Cai C, Long J, Li J, Zhang Z, Hou W, Nie G, Wang Y. Evaluation of activities of daily living using an electronic version of the Longshi Scale in patients with stroke: reliability, consistency, and preference. BMC Med Inform Decis Mak. 2024 May 15;24(1):125. doi: 10.1186/s12911-024-02508-0.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20210812003-FS01
Identifier Type: -
Identifier Source: org_study_id