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

Primary Purpose

Dementia

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Educational programme for all nurses
Training and structured support for nominated key nurses
Facultative train-the-trainer module for key nurses
Printed study material
Supportive material (poster, mugs etc.)
Sponsored by
University of Luebeck
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Dementia focused on measuring nursing home care, physical restraints, dementia, implementation research, cluster-randomized controlled trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Witten/Herdecke University
  • Martin-Luther-University Halle-Wittenberg
  • University of Lübeck
  • University of Hamburg

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Updated original programme

Concise updated programme

Optimized usual care

Arm Description

Educational programme for all nurses (90 min. single information session); training and structured support for nominated key nurses (one-day training workshop); provision of printed study material (evidence-based practice guideline; short versions for nurses, legal guardians, and others; information brochures for relatives); supportive material (poster, mugs etc.)

Training and structured support for nominated key nurses (one-day training workshop); nurses' training will be carried out by key nurses as facultative option; key nurses receive an additional train-the-trainer module to apply the educational programme; provision of printed study material (evidence-based practice guideline; short versions for nurses, legal guardians, and others; information brochures for relatives); supportive material (poster, mugs etc.)

Provision of printed study material (evidence-based practice guideline; short versions for nurses, legal guardians, and others; information brochures for relatives) only

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Residents' quality of life (measured by QoL-AD)
Will be measured by QoL-AD for a randomly selected subgroup of 10% of residents
Falls and fall-related fractures
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

Full Information

First Posted
December 16, 2014
Last Updated
May 2, 2017
Sponsor
University of Luebeck
Collaborators
Martin-Luther-Universität Halle-Wittenberg
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1. Study Identification

Unique Protocol Identification Number
NCT02341898
Brief Title
Implementation of a Multicomponent Intervention to Prevent Physical Restraints in Nursing Home Residents (IMPRINT)
Acronym
IMPRINT
Official Title
Implementation of a Multicomponent Intervention to Prevent Physical Restraints in Nursing Home Residents: a Cluster-randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Luebeck
Collaborators
Martin-Luther-Universität Halle-Wittenberg

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia
Keywords
nursing home care, physical restraints, dementia, implementation research, cluster-randomized controlled trial

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
10800 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Updated original programme
Arm Type
Experimental
Arm Description
Educational programme for all nurses (90 min. single information session); training and structured support for nominated key nurses (one-day training workshop); provision of printed study material (evidence-based practice guideline; short versions for nurses, legal guardians, and others; information brochures for relatives); supportive material (poster, mugs etc.)
Arm Title
Concise updated programme
Arm Type
Experimental
Arm Description
Training and structured support for nominated key nurses (one-day training workshop); nurses' training will be carried out by key nurses as facultative option; key nurses receive an additional train-the-trainer module to apply the educational programme; provision of printed study material (evidence-based practice guideline; short versions for nurses, legal guardians, and others; information brochures for relatives); supportive material (poster, mugs etc.)
Arm Title
Optimized usual care
Arm Type
Active Comparator
Arm Description
Provision of printed study material (evidence-based practice guideline; short versions for nurses, legal guardians, and others; information brochures for relatives) only
Intervention Type
Other
Intervention Name(s)
Educational programme for all nurses
Intervention Type
Other
Intervention Name(s)
Training and structured support for nominated key nurses
Intervention Type
Other
Intervention Name(s)
Facultative train-the-trainer module for key nurses
Intervention Type
Other
Intervention Name(s)
Printed study material
Intervention Type
Other
Intervention Name(s)
Supportive material (poster, mugs etc.)
Primary Outcome Measure Information:
Title
Proportion of residents with at least one physical restraint assessed through direct observation by blinded research assistants
Time Frame
12 Months
Secondary Outcome Measure Information:
Title
Residents' quality of life (measured by QoL-AD)
Description
Will be measured by QoL-AD for a randomly selected subgroup of 10% of residents
Time Frame
12 Months
Title
Falls and fall-related fractures
Time Frame
12 Months
Title
Costs within trial period (cost parameters related to the implementation of the intervention as well as outcome-related cost parameters)
Description
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
Other Pre-specified Outcome Measures:
Title
Process evaluation
Description
Different process parameters will be assessed as e.g. relatives' experiences, staff experiences, leaders' experiences and organizational culture
Time Frame
12 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sascha Köpke, Prof. Dr.
Organizational Affiliation
University of Lübeck
Official's Role
Principal Investigator
Facility Information:
Facility Name
Witten/Herdecke University
City
Witten
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
58448
Country
Germany
Facility Name
Martin-Luther-University Halle-Wittenberg
City
Halle (Saale)
State/Province
Sachsen-Anhalt
ZIP/Postal Code
06112
Country
Germany
Facility Name
University of Lübeck
City
Lübeck
State/Province
Schleswig-Holstein
ZIP/Postal Code
23562
Country
Germany
Facility Name
University of Hamburg
City
Hamburg
ZIP/Postal Code
20146
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
31014546
Citation
Abraham J, Kupfer R, Behncke A, Berger-Hoger B, Icks A, Haastert B, Meyer G, Kopke S, Mohler R. Implementation of a multicomponent intervention to prevent physical restraints in nursing homes (IMPRINT): A pragmatic cluster randomized controlled trial. Int J Nurs Stud. 2019 Aug;96:27-34. doi: 10.1016/j.ijnurstu.2019.03.017. Epub 2019 Apr 4.
Results Reference
derived
PubMed Identifier
26195247
Citation
Abraham J, Mohler R, Henkel A, Kupfer R, Icks A, Dintsios CM, Haastert B, Meyer G, Kopke S. Implementation of a Multicomponent intervention to Prevent Physical Restraints In Nursing home residenTs (IMPRINT): study protocol for a cluster-randomised controlled trial. BMC Geriatr. 2015 Jul 21;15:86. doi: 10.1186/s12877-015-0086-0.
Results Reference
derived
Links:
URL
http://www.leitlinie-fem.de/
Description
project homepage

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

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