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Development and Application of Intelligent Assessment System of Longshi Scale

Development and Application of Intelligent Assessment System of Longshi Scale

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05214638
Enrollment
115
Registered
2022-01-31
Start date
2021-09-10
Completion date
2021-12-31
Last updated
2022-01-31

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

Conditions

Disability Physical, Stroke

Keywords

Stroke, Activities of Daily Living, Electronic Version

Brief summary

The purpose of this study was to verify convenience and feasibility of the novel intelligent Longshi assessment system to provide an accurate and convenient evaluation tool for stroke survivors.

Interventions

None listed

Sponsors

Shenzhen Second People's Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Inclusion Criteria: 1. Stroke survivors * 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 2.

Exclusion criteria

1. Stroke survivors: * 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

Design outcomes

Primary

MeasureTime frameDescription
Consistency of the disability degree evaluated using the electronic version and the paper version of Longshi ScaleWithin 48 hoursWeighted kappa was used to determine the consistency of the disability degree evaluated using the electronic version and the paper version of Longshi Scale. Kappa value ranges from 0 to 1 and the thresholds for kappa reliability are as follows: poor (κ = 0.00-0.20), fair (κ= 0.21-0.40), moderate (κ = 0.41-0.60), good (κ = 0.61-0.80),and very good (κ = 0.81-1.00).

Secondary

MeasureTime frameDescription
Proportion of evaluators' preferenceWithin 48 hoursAfter completing all the evaluations, each evaluator was asked to reveal their preferred version (paper version, electronic version or no preference). Chi-square test was used to compare the proportion of evaluators' preference.
Time requiredWithin 48 hoursTime required in each section of electronic version and paper version of Longshi Scale.
Test-retest reliability of electronic version Longshi ScaleWithin 48 hours after first evaluationWeighted kappa was used to determine test-retest reliability of electronic version Longshi Scale. Kappa value ranges from 0 to 1 and the thresholds for kappa reliability are as follows: poor (κ = 0.00-0.20), fair (κ= 0.21-0.40), moderate (κ = 0.41-0.60), good (κ = 0.61-0.80),and very good (κ = 0.81-1.00).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026