Cerebrovascular disease
Conditions
Interventions
None listed
Sponsors
Fujita Health University
Hamamatsu University School of Medicine, Shinshu University, Toyo University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who have been hospitalized for 2 to 6 weeks. 18-80 years of age who have given informed consent for this study. Have access to a smartphone and agree to install the Exkuma experience sampling tool.
Exclusion criteria
Exclusion criteria: Participants who have difficulty in responding to the experience sampling due to cognitive decline or higher brain dysfunction. Participants who are diagnotised to be in a depressed state. Participants who are hospitalized for Parkinson's disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patient motivation scores for rehabilitation obtained from an experience-sampling questionnaire survey. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patients' pain status, fatigue, depressed mood, apathy, and activity status obtained from an empirical sampling questionnaire survey Basic information on the participants (age, gender, disease, medical history, motor-cognitive function, life function, sleep and activities in the ward, and rehabilitation status are referenced from the medical record and hospital record system) Results of tests of depression, apathy, and other psychiatric conditions at the beginning of the measurement period, and results of individual factor assessments (Brief Resilience Scale Japanese version (BRS-J), Big Five Ten Item Personality Inventory (TIPI-J), etc.). Presence or absence of unusual events during the measurement period (e.g., falls, outings, etc.) | — |
Countries
Japan
Contacts
Public ContactTaiki Yoshida
Fujita Health University Faculty of Rehabilitation, School of Health Sciences
Outcome results
None listed