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N/A N=63 Randomized Single-blind Supportive Care

Effects of Patient-centered Stroke Educating System: a Randomized Controlled Trial

Health Education

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

OutcomeResultp-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
View full record on ClinicalTrials.gov →

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.

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