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Central Utrecht Elderly Care Project

Central Utrecht Elderly Care Project - Om U project

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON34794
Enrollment
5000
Registered
2010-07-26
Start date
2010-10-07
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

chronische ziekten frailty multimorbidity

Interventions

1. Periodic (quarterly) Risk Identification of frailty and Monitoring of care to older people (UPRIM) in electronic medical records of the general practice. 2. UPRIM plus the introduction of a specia

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Potentially frail older people; patients of 60 years and older in general practice setting with one or more of the following three criteria: - multimorbidity (defined as a frailty index score of 0.20 or higher, for eleborate details see chapter 5 of the protocol), AND/OR - polypharmacy (5 or more different drugs in actual chronic use), AND/OR - care gap (more than three years no contact with the general practice, except for the yearly influenzae vaccination)

Exclusion criteria

Exclusion criteria: - terminally ill patients - patients living in an elderly care home or nursing home - patients on a waiting list for an elderly care home or nursing home

Design outcomes

Primary

MeasureTime frame
The primary outcome parameter is change in daily functioning. Daily functioning (ADL) is measured with the Katz 15 questionnaire which is embedded in the Minimal Data Set questionnaire.

Secondary

MeasureTime frame
Secondary outcome parameters are: 1. Quality of life (RAND-36, EQ5D, both embedded in the Minimal Data Set) 2. Care use (number of referrals, admittances, prescriptions, diagnoses and visits) expressed in: a) number of *elective* interventions in secondary care (planned admittances); b) number of *emergency* admittances in secondary care, nursing homes and older people homes homes; c) number of contacts with the general practitioner*s surgeries, outside the regular hours; d) number of contacts with the healthcare assistant, the general practitioner, the general practice assistant and GNPC; e) medication use, dysfunctional and functional polypharmacy; f) consultation with other primary carers (AMW (General Social Work), physiotherapy, homecare); 3. Mortality 4. Cost-effectiveness analysis (CEA) For the CEA, the ratio of differences in the main outcome measure - (I)ADL - between the three groups and differences in costs will be analyzed. 5. Patient satisfaction Patient satisfaction will be measured in the Minimal Data Set. 6. Comparison of frailty index courses between groups, with particular attention to the proportion of patients with polypharmacy, multimorbidity and a care gap of > 3 years. Secondly, focus on the correlation of frailty index scores with daily functioning and quality of life as reported in the Minimal Data Set. 7. Time spent on informal caring and burden of this care for the informal carer; health status and quality of life of informal carer. The secundary outcome parameters are partly measured with the extraction of routine care data by UPRIM, and partly with data acquired in the Minimal Data Set questionnaires (the MDS for the participants as well as for the informal carers).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)