N/A
N=63
Effects of Patient-centered Stroke Educating System: a Randomized Controlled Trial
Health Education
Bottom Line
View on ClinicalTrials.gov: NCT02591511 ↗Enrolled (actual)
63
Serious AEs
0.0%
Results posted
Sep 2018
Primary outcome: Primary: Stroke Health Education Knowledge Questionnaire — 29.07; 28.00 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- smart phone and pad (Device); stroke-related health education manual (Other)
- Age
- Adult, Older Adult · 20+ yrs
- Sex
- All
- Sponsor
- Taipei Medical University
- Primary completion
- Oct 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Stroke Health Education Knowledge Questionnaire |
29.07; 28.00 | — |
Summary
The aim of this study is to establish PAtient-Centered Computerized Educating System for Stroke (PACCESS) for patients with different demands and lack of knowledge.Those in the intervention group will receive the PACCESS and the control groups will receive traditional health education to test the effects of PACCESS in increasing clinical decision-making, health behavior, activities of daily living and knowledge of stroke, and health care quality.
Eligibility Criteria
Inclusion Criteria
- first time diagnosis of stroke (International Classification of Diseases, ninth revision, clinical modification [ICD-9] codes) of cerebral hemorrhage (ICD-9, 431) or cerebral infarction (ICD 9, 434)
- ability to follow instructions and complete the interviews
- having a designated caregiver who agrees to participate in the survey
- >6 years of education
- have smartphone or the other mobile device can download the APP from internet.
Exclusion Criteria
- cognitive impairment (Mini-Mental State Examination (MMSE scores<24)
- having major mental diseases (i.e., depression, dementia, delirium, etc.)
- the inability to read/answer questionnaires
Data sourced from ClinicalTrials.gov (NCT02591511). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.