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SCREAM

Supporting Clinical Rules Engine in the Adjustment of Medication

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26219
Enrollment
4000
Registered
2015-04-02
Start date
2013-06-01
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

Polypharmacy Medication Therapy Management Decision Support Systems Management Aged Medication review

Interventions

A clinical decision support system, the CRR (clinical rule reporter) will be used to weekly screen medication list, laboratory values and medical history in order to obtain potential clinical relevant

Sponsors

Atrium-Orbis Medisch Centrum
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Residents living in a nursing home in the Netherlands. The nursing homes are able to deliver the medication and lab data electronically

Exclusion criteria

Exclusion criteria: When the inclusion criteria can't be met

Design outcomes

Primary

MeasureTime frame
The primary outcome variable in this study is the proportion of patients with at least one of the events, including hospital referrals (i.e. referral to a specialist, emergency department visit and hospital admission), delirium, falls, and/or deaths. To this end the study will assess the differences between regular care (control group) and regular care + CRR (intervention group).

Secondary

MeasureTime frame
As secondary endpoints, the same outcome variable will be used to analyse the possible differences between institutions, to separately analyse psychogeriatric and somatic wards, to analyse the medication related events, and to separately analyse each of the parameters included in the combined endpoint (hospital referrals, delirium, falls, and/or deaths). Also the quality of life, the MAI and a cost evaluation will be performed for both control and intervention group.

Contacts

Public ContactPHM van der Kuy

Atrium-Orbis Medisch Centrum - Dr. H van der Hoofplein 1

h.vanderkuy@orbisconcern.nl088-4597709

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)