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Onset PrevenTIon of Urinary Retention in Orthopaedic Nursing and Rehabilitation (OPTION)

Primary Purpose

Urinary Retention, Hip Fractures, Hip Arthritis

Status
Active
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
: A support program to facilitate implementation of evidence-based practice for postoperative urinary retention
Sponsored by
Örebro University, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Urinary Retention focused on measuring Orthopedics, Implementation, Research utilization

Eligibility Criteria

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

Inclusion Criteria: Orthopaedic units in Sweden performing hip surgery. -

Exclusion Criteria: Orthopaedic units in Sweden not performing hip surgery

-

Sites / Locations

  • Sjukhuset Arvika
  • Danderyds sjukhus
  • Höglandssjukhuset Eksjö
  • Enköpings lasarett
  • Mälarsjukhuset
  • Gävle sjukhus
  • Karolinska University Hospital, Huddinge
  • Hudiksvalls sjukhus
  • Capio Ortopediska huset
  • Karlskoga Lasarett
  • Vrinnevisjukhuset
  • Nyköpings lasarett
  • Södersjukhuset
  • Södertälje sjukhus
  • Sjukhuset Torsby
  • Västmanlands sjukhus
  • Örebro University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

A support program to facilitate implementation of EBP for postoperative urinary retention

Control-No support program

Arm Description

12- month support program. Multi-professional facilitator-teams will be supported by a 12-month support program including seminars and monthly supervision (e-discussion forum and group teleconferences) to develop an awareness of, and skills in facilitating implementation of evidence/EBP in clinical everyday care.

No support program

Outcomes

Primary Outcome Measures

Adherence to UR guidelines in the care of patients undergoing hip surgery.
Adherence to national urinary retention guidelines documented in the patients' medical record

Secondary Outcome Measures

Number of hip surgery patients with UR
Number of hip surgery patients with UR documented in the patients' medical record
Patient participation
The Patient Preferences for Patient Participation tool (The 4Ps)
Costs related to UR
Costs for device and labour for bladder scanning and urinary catheterization
The IFs', staff's, and managers' experience of UR care
Investigated with qualitative interviews
The IFs', staff's, and managers' experience of the facilitation program
Investigated with qualitative interviews
The experience of people undergoing hip surgery, regarding UR, UR care.
Investigated with qualitative interviews
The impact of a knowledge translation support program on the peoples' experience of the above
Investigated with qualitative interviews

Full Information

First Posted
December 23, 2020
Last Updated
April 19, 2022
Sponsor
Örebro University, Sweden
Collaborators
Linkoeping University, Karolinska Institutet
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1. Study Identification

Unique Protocol Identification Number
NCT04700969
Brief Title
Onset PrevenTIon of Urinary Retention in Orthopaedic Nursing and Rehabilitation
Acronym
OPTION
Official Title
Onset PrevenTIon of Urinary Retention in Orthopaedic Nursing and Rehabilitation, OPTION - a Knowledge Implementation Study on a Facilitation Strategy for Multi-professional Clinical Champion Teams
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 15, 2020 (Actual)
Primary Completion Date
May 30, 2023 (Anticipated)
Study Completion Date
May 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Örebro University, Sweden
Collaborators
Linkoeping University, Karolinska Institutet

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Urinary retention (UR) is a common problem in older people undergoing hip surgery. Untreated UR can lead to bladder distention and a permanent damage of the bladder, which can cause both physical and psychical suffering as well as increased costs for society. Even if national and international practice guidelines are in place for handling UR within the health care system, many fail to comply with them. Compliance to clinical practice guidelines are improved if different professions and managers collaborate as a team. In OPTION (Onset PrevenTIon of urinary retention in Orthopedic Nursing and rehabilitation) the investigators will coach multi-professional local facilitator teams in knowledge translation and implementation of UR practice as well as investigate the effects of such evidence-based practice in orthopedic nursing and rehabilitation. Implementation of research-based knowledge in evidence-based practice within an organization is complex with several known interacting factors. In a health care system these factors can be the care context, knowledge (innovation) and how the organization facilitates such implementations. The implementation strategy of OPTION utilize established theories of facilitation of knowledge implementation considering evidence and context with focus on leadership. The intervention consists of seminars and systematic support for implementation of UR-guidelines OPTION combine studies of adherence to evidence based practice regarding UR for patients over 65 years old that has undergone hip surgery and the health economic aspects of it. OPTION also contribute with improvements and increased knowledge regarding strategies to implement evidence based health care that can be used in other areas than UR and hip surgeries.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Retention, Hip Fractures, Hip Arthritis
Keywords
Orthopedics, Implementation, Research utilization

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A support program to facilitate implementation of EBP for postoperative urinary retention
Arm Type
Experimental
Arm Description
12- month support program. Multi-professional facilitator-teams will be supported by a 12-month support program including seminars and monthly supervision (e-discussion forum and group teleconferences) to develop an awareness of, and skills in facilitating implementation of evidence/EBP in clinical everyday care.
Arm Title
Control-No support program
Arm Type
No Intervention
Arm Description
No support program
Intervention Type
Other
Intervention Name(s)
: A support program to facilitate implementation of evidence-based practice for postoperative urinary retention
Intervention Description
A 12-month implementation support program for multi-professional internal facilitator teams
Primary Outcome Measure Information:
Title
Adherence to UR guidelines in the care of patients undergoing hip surgery.
Description
Adherence to national urinary retention guidelines documented in the patients' medical record
Time Frame
Change from base line to 1 year after the intervention
Secondary Outcome Measure Information:
Title
Number of hip surgery patients with UR
Description
Number of hip surgery patients with UR documented in the patients' medical record
Time Frame
Change from base line to 1 year after the intervention
Title
Patient participation
Description
The Patient Preferences for Patient Participation tool (The 4Ps)
Time Frame
Change from base line to 1 year after the intervention
Title
Costs related to UR
Description
Costs for device and labour for bladder scanning and urinary catheterization
Time Frame
Change from base line to 1 year after the intervention
Title
The IFs', staff's, and managers' experience of UR care
Description
Investigated with qualitative interviews
Time Frame
Change from base line to 1 year after the intervention
Title
The IFs', staff's, and managers' experience of the facilitation program
Description
Investigated with qualitative interviews
Time Frame
1 year after the intervention
Title
The experience of people undergoing hip surgery, regarding UR, UR care.
Description
Investigated with qualitative interviews
Time Frame
Change from base line to 1 year after the intervention
Title
The impact of a knowledge translation support program on the peoples' experience of the above
Description
Investigated with qualitative interviews
Time Frame
Change from base line to 1 year after the intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Orthopaedic units in Sweden performing hip surgery. - Exclusion Criteria: Orthopaedic units in Sweden not performing hip surgery -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Hälleberg Nyman, PHD
Organizational Affiliation
Örebro University, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sjukhuset Arvika
City
Arvika
Country
Sweden
Facility Name
Danderyds sjukhus
City
Danderyd
Country
Sweden
Facility Name
Höglandssjukhuset Eksjö
City
Eksjö
Country
Sweden
Facility Name
Enköpings lasarett
City
Enköping
Country
Sweden
Facility Name
Mälarsjukhuset
City
Eskilstuna
Country
Sweden
Facility Name
Gävle sjukhus
City
Gävle
Country
Sweden
Facility Name
Karolinska University Hospital, Huddinge
City
Huddinge
Country
Sweden
Facility Name
Hudiksvalls sjukhus
City
Hudiksvall
Country
Sweden
Facility Name
Capio Ortopediska huset
City
Johanneshov
Country
Sweden
Facility Name
Karlskoga Lasarett
City
Karlskoga
Country
Sweden
Facility Name
Vrinnevisjukhuset
City
Norrköping
Country
Sweden
Facility Name
Nyköpings lasarett
City
Nyköping
Country
Sweden
Facility Name
Södersjukhuset
City
Stockholm
Country
Sweden
Facility Name
Södertälje sjukhus
City
Södertälje
Country
Sweden
Facility Name
Sjukhuset Torsby
City
Torsby
Country
Sweden
Facility Name
Västmanlands sjukhus
City
Västerås
Country
Sweden
Facility Name
Örebro University Hospital
City
Örebro
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
34174917
Citation
Eldh AC, Joelsson-Alm E, Wretenberg P, Halleberg-Nyman M. Onset PrevenTIon of urinary retention in Orthopaedic Nursing and rehabilitation, OPTION-a study protocol for a randomised trial by a multi-professional facilitator team and their first-line managers' implementation strategy. Implement Sci. 2021 Jun 26;16(1):65. doi: 10.1186/s13012-021-01135-x.
Results Reference
derived

Learn more about this trial

Onset PrevenTIon of Urinary Retention in Orthopaedic Nursing and Rehabilitation

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