F05
Conditions
Interventions
Group 1: INTERVENTION
The intervention will be conducted by a mobility-team between 9.00 and 11.00 p.m.
The intervention begins on day 1, or after consent and randomization. The duration of the interv
Sponsors
Universitätsklinikum Schleswig-Holstein, Pflegeforschung, Campus Kiel
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: a) age =18 years, B) Richmond Agitation Sedation Scale = -3 (respond to command), c) are susceptible to delirium, d) are mobilizable, e) expected min. one night in intensive care
Exclusion criteria
Exclusion criteria: a) condition with the expectation of death in the next 72h, b) No approval of the study, c) Rejection of evening mobilization, d) Pre-existing immobility, e) Contraindication to mobilization
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of delirium. Patients will be assessed for delirium three times in 24h using the Confusion Assessment Method for the Intensive Care Unit | — |
Secondary
| Measure | Time frame |
|---|---|
| Following data will be extracted from patients charts Presence of delirium, assessed 3x/24h by Confusion Assessment Method for the Intensive Care Unit Mortality Duration of mechanically ventilation in days Length of stay in days Mobilisations (time, duration, level) Mobility-related complications Independency assessed by Barthel-Index Costs by Diagnosis Related Groups | — |
Countries
Germany, United Kingdom
Contacts
Public ContactPeter Nydahl
Universitätsklinikum Schleswig-Holstein, Pflegeforschung, Campus Kiel
Outcome results
None listed