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Effects of using a lost items finder on caregiving stress for family caregivers of patients with dementia

Effects of using a lost items finder on caregiving stress for family caregivers of patients with dementia: a pilot randomized controlled trial - Effects of using a lost items finder on caregiving stress for family caregivers of patients with dementia: a pilot randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038364
Enrollment
20
Registered
2020-02-01
Start date
2020-02-04
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

Interventions

Lend a lost items finder to the intervention group, and the patient and caregiver will use it for two months. The control group has no lost items finder and receive normal treatment.

Sponsors

Department of Human Health Sciences, Graduate School of Medicine, Kyoto University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient 1. People with dementia, mild cognitive impairment or subjective cognitive impairment who have losing problems, on average more than twice a month. 2. Patients who can understand the significance of this study. Family caregiver 1. Family caregivers who live with the patient, accompany the patient and take care of them everyday. 2. Family caregivers who have no cognitive impairment 3. Family caregivers who can use the lost items finder correctly according to the instructions. 4. Family caregivers who agree to participate in this study and provide informed consent.

Exclusion criteria

Exclusion criteria: Patient 1. ADL is low and almost every day life is assisted. Family caregiver 1. Family caregivers who are using the lost items finder at home already. 2. Family caregivers who have problems with vision or hearing.

Design outcomes

Primary

MeasureTime frame
Using the Japanese version of the Zarit Caregiver Burden Interview to assess the change of caregiving stress from baseline to two months after the intervention

Secondary

MeasureTime frame
Secondary outcome measures include the Japanese version for the Revised Scale for Caregiving Self-Efficacy, the Japanese version of the Burnout Measure, and reduction of finding time and finding frequency.

Countries

Japan

Contacts

Public ContactZhouyuan Peng

Graduate School of Medicine Kyoto university Human Health Sciences

pengzhy9@mail2.sysu.edu.cn075-751-3969

Outcome results

None listed

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