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Study on ADL Assessment and Rehabilitation for Individuals with Dementia using Photo Assessment and ZOOM

A Study on Standardizing Non-Visit-Based ADL Assessment and Intervention Systems to Support the maintenance of living at home for Individuals with Dementia - A Study on Standardizing Non-Visit-Based ADL Assessment and Intervention Systems to Support the maintenance of living at home for Individuals with Dementia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051635
Enrollment
45
Registered
2023-08-01
Start date
2023-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Dementia(Alzheimer&#39

Interventions

Intervention Group (45 cases): 1.Conduct baseline assessments (PSMS, IADL, PADA-D, MMSE, NPI, GDS, ZBI) for the participants and their caregivers. 2. Provide caregivers with cameras to take home pho

Sponsors

Osaka University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: #The etiology of dementia is limited to Alzheimer's disease, Lewy body dementia, and frontotemporal dementia(dementia defined as CDR of 1 or higher). #For MCI, MMSE score should be 24 or higher, and CDR should be 0.5. #Participants aged 40 or above but less than 90 at the time of obtaining consent. #Participants who are living together with a caregiver who is well acquainted with the condition of the target individual in their own home. In the case of individuals living alone, there should be a supporting individual who is familiar with the condition of the target individual. #Participants who can provide informed consent both in writing and orally based on their own free will, or participants for whom appropriate surrogate consent can be obtained to confirm their willingness.

Exclusion criteria

Exclusion criteria: #Patients with dementia or mild cognitive impairment due to medication or cerebrovascular disorders. #Patients with severe medical conditions. #Patients with coexisting psychiatric disorders such as schizophrenia, mood disorders, or substance abuse. #Patients deemed unsuitable by the principal investigator or co-investigators. #Patients deemed ineligible for participation by their attending physician. #Individuals who require assistance in daily living activities primarily due to physical functional decline. #Individuals who require constant caregiving due to cognitive decline. #Other individuals deemed unsuitable by the principal investigator or co-investigators.

Design outcomes

Primary

MeasureTime frame
Activities of Daily Living;PADA-D (Process Analysis of Daily Activity for Dementia)

Secondary

MeasureTime frame
PSMS(Physical Self-Maintenance Scale),IADL (Lawton Instrumental Activities of Daily Living Scale),MMSE(Mini Mental State Examination), GDS(Geriatric Depression Scale), NPI(Neuropsychiatric Inventory), ZBI(Zarit Caregiver Burden Interview)

Countries

Japan

Contacts

Public ContactMaki Hotta

Osaka University Department of Psychiatry, Osaka University Graduate School of Medicin

komaki@psy.med.osaka-u.ac.jp06-6879-3051

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026