Radboud University Nijmegen Medical Centre
Nijmegen, Gelderland, 6500 HB, Netherlands
NCT Number: NCT01273116
The current organization of hospital care for older patients with complex healthcare needs is of insufficient quality, safety and efficiency. Frail older patients have a higher risk for development of complications and consequently a higher length of hospital stay, a higher risk of functional decline, and higher care needs after discharge. As nearly half of the patients admitted to Dutch hospitals is over 65 years, it is highly necessary to adapt the organization of hospital care to their needs. Besides having introduced the medical specialty geriatrics, hospital management has not started to provide hospital wide healthcare tailored to frail older patients. Therefore, the purpose of this study is to develop and examine the effectiveness of an intervention program for frail older patients admitted to hospital aimed at preventing functional decline and other hospital related negative outcomes.
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Notify Me70 year and older
All sexes
Interventional
Not applicable
Nijmegen, Gelderland, 6500 HB, Netherlands
The long-term objective of this study is to examine the effectiveness and efficiency of an intervention program for frail older patients admitted to hospital. The specific aims are:
We expect that older patients who participate in the intervention program after one year of implementation, compared to patients who were admitted to hospital before implementation of the intervention program, will:
Additionally, we expect that the knowledge and attitudes toward care for older patients among nurses and physicians will change positively during implementation of the intervention program.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Every patient aged ≥70 years will be screened for frailty. (For) every frail patient:
Hospital staff will be educated, disease-specific guidelines will be adapted to frail older patients.
Time frame: during hospital stay
cumulative incidence in delirium, falls, functional decline (GARS), and loss of cognition (MMSE)
Time frame: 2 weeks before admission, discharge, 3 months after discharge
maintenance or improvement of functional status (Groningen Activity Restriction Scale GARS)):
Time frame: during hospital stay
incidence delirium (as judged by an independent physician, structured by daily application of the Confusion Assessment Method (CAM) and Delirium Observation Scale (DOS))
Time frame: before implementation and one year after implementation of CWS InHospital
Consumer Quality Indicator CWS In Hospital: to address autonomy of patients, developed by own researchers
Time frame: discharge and 3 months follow-up
OPROCS = cumulative outcome measure functional ability and quality of life etc. as determined by the elderly (Minimum Data Set)
Time frame: before and one year after implementation CWS InHospital
recognition of delirium by medical staff (nurses and doctors) compared to diagnoses by independent physician using CAM and DRS-r-98
Time frame: within 1 month after discharge
readmissions within 1 month after discharge (Minimum Data Set, electronic health record)
Time frame: from admission to 3 months after discharge patient
objective burden of care among informal caregivers (Minimum Data Set)
Time frame: from admission to 3 months after discharge
expressed in incremental cost-effectiveness ratio (length of stay; use of health care services (MDS), quality of life) primary outcomes as nominator, and expressed in costs per quality adjusted life years, all related to total health care costs from a societal perspective, from admission to three months following discharge
Radboud University Medical Center
Other
Towards an In Hospital CARE AND WELFARE STANDARD for Frail Elderly
Acronym: CWSInHosp
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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