Usability of Cognitive Improvement Software in Cognitively Impaired Patients: Pilot Study
Active, not recruiting
- Conditions
- Mild Cognitive Impairment
- Interventions
- Other: Cognitive improvement software
- Registration Number
- NCT05634161
- Lead Sponsor
- Seoul National University Hospital
- Brief Summary
Usability study of software application that provide digitized cognitive intervention therapy for cognitively impaired patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Male and Female patients, 55~85 years
- Adequate vision, hearing and speaking for neuropsychological testing
- No difficulty in using mobile application using smartphone
- Patients with subjective memory complaints, confirmed by informants
- Cognitive impairment of SD 1 or greater from the age-adjusted normal range in Memory domain in CERAD-NP battery
- Global CDR 0.5 ~ 1
- Korean speaker
- Have an identified trial partner
- All subjects signed written consent
Exclusion Criteria
- Those unable to provide consent
- History of transient ischemic attack, stroke, brain tumor
- History of diagnosis of major depression
- Symptoms that may interfere with the subject's testing procedure
- Cerebral hemorrhage
- Central nervous system infections
- Prohibited concomitant medication
- Known or suspected history of drug or alcohol abuse
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Cognitive Improvement software Cognitive improvement software Usability assessment of cognitive improvement software
- Primary Outcome Measures
Name Time Method Usability: Based on scenarios Single-point evaluation (baseline)
- Secondary Outcome Measures
Name Time Method Changes in ADCS-ADL After 12 weeks of system usage Changes in self-reported quality of life After 12 weeks of system usage Changes in blood biomarker After 12 weeks of system usage Usability: Based on user survey Single-point evaluation (baseline) Usability: Based on hemodynamic responses Single-point evaluation (baseline) Changes in Adas-cog After 12 weeks of system usage
Trial Locations
- Locations (1)
Seoul Metropolitan Government Seoul National University Boramae Medical Center
🇰🇷Seoul, Korea, Republic of