NCT Number: NCT02341898
Implementation of a Multicomponent Intervention to Prevent Physical Restraints in Nursing Home Residents (IMPRINT)
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.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Witten/Herdecke University, Witten, North Rhine-Westphalia, Germany
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Cluster level
Inclusion criteria
- randomly selected nursing homes in each region; no specific inclusion criteria will be applied
Exclusion criteria
- no specific exclusion criteria will be applied
Individual level
Inclusion criteria
- all residents within the cluster present on the day of data collection
- all residents newly admitted to clusters during follow-up and present on the day of follow-up data collection
Exclusion criteria
- no specific exclusion criteria will be applied
Treatment and study plan
Training and structured support for nominated key nurses
OtherFacultative train-the-trainer module for key nurses
OtherPrinted study material
OtherSupportive material (poster, mugs etc.)
OtherPrimary outcomes
-
Proportion of residents with at least one physical restraint assessed through direct observation by blinded research assistants
Time frame: 12 Months
Secondary outcomes
-
Residents' quality of life (measured by QoL-AD)
Time frame: 12 Months
Will be measured by QoL-AD for a randomly selected subgroup of 10% of residents
-
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)
Time frame: 12 Months
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
Other outcomes
-
Process evaluation
Time frame: 12 Months
Different process parameters will be assessed as e.g. relatives' experiences, staff experiences, leaders' experiences and organizational culture
Sponsors and collaborators
Lead sponsor
University of Luebeck
Other
Collaborators
- Martin-Luther-Universität Halle-Wittenberg
Registry information
Official study title
Implementation of a Multicomponent Intervention to Prevent Physical Restraints in Nursing Home Residents: a Cluster-randomized Controlled Trial
Acronym: IMPRINT
Important dates
- Study start
- 2015
- Primary completion
- 2017
- Study completion
- 2017
- First posted
- Jan 19, 2015
- Registry last updated
- May 3, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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