Background: Physical restraints as bedrails and belts are still regularly applied in German nursing homes despite clear evidence showing their lack of effectiveness and safety. In a cluster-randomized controlled trial, the efficacy of a guideline-based multicomponent intervention has been shown with a significant reduction in physical restraints use without adverse events. The present study aims to apply different versions of the original intervention in nursing home residents in four different regions throughout Germany in order to evaluate the effectiveness of the programme. Methods/Design: Pragmatic cluster-randomized controlled trial comparing two intervention groups ((1) updated original programme and (2) brief version of the updated programme) with a control group (3) receiving printed study materials (optimized usual care). Intervention (1) consists of an information programme for all nurses, additional training and structured support for nominated key nurses, and provision of printed study material and other supportive material. For intervention (2) nurses' training is only optional carried out facultatively by key nurses who have received an additional train-the-trainer module. The control group (3) receives printed study material only. Overall, 120 nursing homes including approximately 10800 residents will be recruited, randomized to one of the three groups and followed up for 12 months. The primary outcome is defined as proportion of residents with at least one physical restraint at 12 months. Physical restraint use will be assessed by direct observation. Secondary outcomes are residents' quality of life as well as safety parameters as i.g. falls and fall-related fractures. Process and cost measures will also be assessed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
10,800
Witten/Herdecke University
Witten, North Rhine-Westphalia, Germany
Martin-Luther-University Halle-Wittenberg
Halle, Saxony-Anhalt, Germany
University of Lübeck
Lübeck, Schleswig-Holstein, Germany
University of Hamburg
Hamburg, Germany
Proportion of residents with at least one physical restraint assessed through direct observation by blinded research assistants
Time frame: 12 Months
Residents' quality of life (measured by QoL-AD)
Will be measured by QoL-AD for a randomly selected subgroup of 10% of residents
Time frame: 12 Months
Falls and fall-related fractures
Time frame: 12 Months
Costs within trial period (cost parameters related to the implementation of the intervention as well as outcome-related cost parameters)
For economic evaluation cost parameters related to the implementation of the intervention will be collected as well as outcome-related costparameters; explicit trial-associated will not be taken into account
Time frame: 12 Months
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