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The Hospital Elder Life Program (HELP) a multicomponent targeted intervention to prevent delirium in hospitalized older patients. A study on efficacy and cost-effectiveness in Dutch health care.

The Hospital Elder Life Program (HELP) a multicomponent targeted intervention to prevent delirium in hospitalized older patients. A study on efficacy and cost-effectiveness in Dutch health care. - (Cost-)effectiveness study on HELP, a delirium prevention program.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37868
Enrollment
1080
Registered
2012-09-27
Start date
2012-10-01
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

acute confusion loss of orientation

Interventions

HELP has four unique components: 1. The program provides standardized protocols targeted toward six delirium risk factors. 2. A multidisciplinary geriatric team, with a central role for the Nurse P

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -Patients are at least 70 years of age -Have no delirium at the time of admission, and are considered at risk for delirium at admission as determined by the VMS criteria (www.vmsveiligheid.nl) According to these criteria at least on of the following three questions has to be answered positive to include a patient with an increased risk of delirium: - Dou you have memory problems? - During the past 24-hours did you need assistance for your daily self-care? - Were you confused during earlier hospital admissions or illnesses?

Exclusion criteria

Exclusion criteria: -Older patients in life threatening situations or with a terminal illness at admission. -Patients with an expected hospital stay of 24 hours or less. -Patients who are legally incapable of participating or with precluded verbal communication. -In case of a language barrier. -Patients with profound aphasia. -Patients with intubation or respiratory isolation

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is the incidence of delirium. Secondary outcomes include delirium duration (number of days) and severity, length of stay, care consumption up to three months after admission, experienced quality of the care process by patients, family, professionals and trained volunteers.

Secondary

MeasureTime frame
Secondary outcomes include delirium duration (number of days) and severity, length of stay, care consumption up to three months after admission, experienced quality of the care process by patients, family, professionals and trained volunteers.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)