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Implementation of social prescription starting from a nursing university to improve the life functions of elderly people living in the community during outpatient visits

Association between social prescribing and life functioning in community-dwelling older people on outpatient visits, originating from a nursing university - Association between social prescribing and life functioning in community-dwelling older people on outpatient visits, originating from a nursing university

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055326
Enrollment
60
Registered
2024-09-01
Start date
2024-11-01
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

Hypertension, Dyslipidemia, Type2 Diabetes, CKD, Ischemic heart disease, Osteoarthritis, Low back pain

Interventions

Standard care plus 6 months of social prescribing Standard care

Sponsors

SHONAN KAMAKURA UNIVERSITY OF MEDICAL SCIENCES
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Persons with a current medical history of hypertension, dyslipidemia, type II diabetes, chronic renal dysfunction, ischemic heart disease, knee osteoarthritis, or orthopedic disease such as low back pain. 2. Persons who can participate in group walks. 3. Persons currently attending outpatient clinics at participating facilities. 4. Persons who have face-to-face or non-face-to-face interactions with people other than those living in their household less than once a week

Exclusion criteria

Exclusion criteria: 1. Persons with a history of hospitalization due to an underlying disease within the past six months or whose underlying disease is poorly controlled. 2. Persons who need to limit their physical activity. 3. Persons who do not have cognitive decline that would limit their activities based on clinical judgment. 4. Any other person the research director judges as inappropriate as a research subject.

Design outcomes

Primary

MeasureTime frame
Primary outcomes related to feasibility (successful rate of subject recruitment, study participation period, data collection compliance, acceptability of intervention method, blood test result acquisition rate, intraclass correlation in clusters)

Secondary

MeasureTime frame
Indicators related to evaluation of intervention effectiveness and safety (degree of loneliness, degree of frailty, degree of depression, walking speed, posture evaluation, general attributes, blood test results, adverse events, etc.)

Countries

Japan

Contacts

Public ContactMasumi Takei

SHONAN KAMAKURA UNIVERSITY OF MEDICAL SCIENCES. Nursing Faculty

m.takei@sku.ac.jp0467383101

Outcome results

None listed

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