Clinical Trials Directory

Trials / Completed

CompletedNCT02341898

Implementation of a Multicomponent Intervention to Prevent Physical Restraints in Nursing Home Residents (IMPRINT)

Implementation of a Multicomponent Intervention to Prevent Physical Restraints in Nursing Home Residents: a Cluster-randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10,800 (actual)
Sponsor
University of Luebeck · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHEREducational programme for all nurses
OTHERTraining and structured support for nominated key nurses
OTHERFacultative train-the-trainer module for key nurses
OTHERPrinted study material
OTHERSupportive material (poster, mugs etc.)

Timeline

Start date
2015-03-01
Primary completion
2017-03-01
Completion
2017-03-01
First posted
2015-01-19
Last updated
2017-05-03

Locations

4 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT02341898. Inclusion in this directory is not an endorsement.