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A single-arm feasibility study to examine the effects of ICT-based social prescribing with wellbeing coordinators on improving wellbeing in isolated older adults

A single-arm feasibility study to examine the effects of ICT-based social prescribing with wellbeing coordinators on improving wellbeing in isolated older adults - A single-arm feasibility study to examine the effects of ICT-based social prescribing with wellbeing coordinators on improving wellbeing in isolated older adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056460
Enrollment
30
Registered
2024-12-15
Start date
2024-12-04
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

Hypertension, Dyslipidemia, Type 2 Diabetes Mellitus, Chronic Kidney Disease, Ischemic Heart Disease, and other Internal Medicine Conditions,As well as orthopedic diseases such as knee osteoarthritis and low back pain.

Interventions

Social describing for 6 months with standard treatment

Sponsors

Teikyo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Aged 65 years or older. 2) Individuals meeting any of the following criteria for social isolation: (a) Less than one contact per week with a person other than cohabitants. (b) Living alone. (c) Any other case where a physician deems the individual to be at high risk of social isolation. 3) Individuals with chronic diseases: internal diseases such as hypertension, dyslipidemia, type 2 diabetes, chronic kidney disease, ischemic heart disease, as well as orthopedic diseases such as knee osteoarthritis and low back pain. 4) Individuals who own a smartphone.

Exclusion criteria

Exclusion criteria: 1) Individuals deemed to have communication difficulties due to cognitive impairment or hearing loss. 2) Any other individual whom the principal investigator deems unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
Items related to the feasibility of a large-scale study: recruitment success rate, data collection compliance, acceptability of intervention methods, success rate of link workers in facilitating activities, and rate of obtaining blood test results.

Secondary

MeasureTime frame
Indicators necessary to assess the effectiveness and safety of the intervention: subjective well-being, physical activity levels, degree of frailty, degree of social isolation, general blood test values, facilitated community activities, satisfaction with ICT tools, adverse events, etc.

Countries

Japan

Contacts

Public ContactShinji Sato

Teikyo University Faculty of Medical Technology

shinjisato2005hawaii@yahoo.co.jp0120-508-739

Outcome results

None listed

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