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Completed

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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Key information

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

Loading trial locations.

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

Educational programme for all nurses

Other

Training and structured support for nominated key nurses

Other

Facultative train-the-trainer module for key nurses

Other

Printed study material

Other

Supportive material (poster, mugs etc.)

Other

Primary outcomes

  1. Proportion of residents with at least one physical restraint assessed through direct observation by blinded research assistants

    Time frame: 12 Months

Secondary outcomes

  1. 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

  2. Falls and fall-related fractures

    Time frame: 12 Months

  3. 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

  1. 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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