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Central Utrecht Elderly Care Project 'Om U': “Somebody who knows what’s going on and can see things from my side.”

Central Utrecht Elderly Care Project.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26480
Enrollment
3092
Registered
2010-04-14
Start date
2010-10-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

frailty, multimorbidity, complex care needs, daily functioning, quality of life. kwetsbaarheid, multimorbiditeit, complexe zorgbehoefte, dagelijks functioneren, kwaliteit van leven.

Interventions

1. Group A: Utrecht Periodic Risc Identification and Monitoring (UPRIM). UPRIM is a method adapted for elderly care also known in the literature as panel management. It entails preventive identifica
functional decline, falling, mood and loneliness, urinary incontinence, malnutrition, visual impai

Sponsors

University Medical Center Utrecht P.O. box 85500 3508 GA Utrecht 088 75 555 55
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The target group of this project is made up of potentially frail older people in general practice setting, who are defined as persons of 60 years and older with: 1. Multimorbidity (defined as a moderate-to-high frailty index score, which is a reflection of the proportion of health deficits present.), AND / OR; 2. Polypharmacy (defined as the actual chronic use of 4 or more different medications), AND / OR; 3. A care gap in primary care of > 3 years, except for the yearly influenza vaccination.

Exclusion criteria

Exclusion criteria: 1. Terminally ill patients; 2. Patients living in or on a waiting list for an elderly home or nursing home.

Design outcomes

Primary

MeasureTime frame
The primary outcome parameter is change in daily functioning. General functioning (ADL and IADL) is measured with the Katz 15 questionnaire, which is included in the minimal data set (MDS), the questionnaire used in this project.

Secondary

MeasureTime frame
1. Quality of life, as registered with the RAND-36, partially included in the MDS; 2. Health care consumption, as expressed in: A. Number of ‘elective’ admissions to hospitals, nursing homes and elderly homes; B. Number of emergency department visits and ‘emergency’ admissions to hospitals, nursing homes and elderly homes; C. Number of contacts with the GP’s surgeries, outside the regular hours; D. Number of contacts with the healthcare assistant, the GP, the general practice assistant and the GNPC; E. Medication use, dysfunctional and functional polypharmacy; F. Consultation with other primary carers (General Social Work, elderly care, physical therapy, homecare). 3. Mortality, as registered in the EMR of the GP, and confirmed by dead certificates of the municipal administration (gemeentelijke basisadministratie); 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 with -changes in- primary health care. Patient satisfaction will be measured in the MDS; 6. Comparison of frailty index courses between groups, and particular attention to the proportion of patients with polypharmacy, multimorbidity and a care gap of > 3 years, and the correlation between the frailty index score and daily functioning and quality of life; 7. Time spent on informal caring and burden of care for informal carer; health status and quality of life of informal carer.

Contacts

Public ContactC.I.M. Heijst, van

Postbus 8605

s.van.heijst@rhijnhuysen.nl+31 (0)30 2953622

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)