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Clinical Trials in Sweden / NCT04700969
Active, not recruiting Not applicable

Onset PrevenTIon of Urinary Retention in Orthopaedic Nursing and Rehabilitation

NCT04700969 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2020-12-15
Last updated
2025-03-21

Condition(s) studied

Urinary RetentionHip FracturesHip Arthritis

Investigational drug(s) / intervention(s)

: A support program to facilitate implementation of evidence-based practice for postoperative urinary retention

: A support program to facilitate implementation of evidence-based practice for postoperative urinary retention: A 12-month implementation support program for multi-professional internal facilitator teams

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Orthopaedic units in Sweden performing hip surgery. - Exclusion Criteria: Orthopaedic units in Sweden not performing hip surgery \-

Primary outcome measure(s)

Trial sites (17)

FacilityCityRegionStatus
Sjukhuset Arvika Arvika Sweden
Danderyds sjukhus Danderyd Sweden
Höglandssjukhuset Eksjö Eksjö Sweden
Enköpings lasarett Enköping Sweden
Mälarsjukhuset Eskilstuna Sweden
Karolinska University Hospital, Huddinge Huddinge Sweden
Capio Ortopediska huset Johanneshov Sweden
Karlskoga Lasarett Karlskoga Sweden
Capio Specialistvård Motala Motala Sweden
Vrinnevisjukhuset Norrköping Sweden
Norrtälje Sjukhus Norrtälje Sweden
Nyköpings lasarett Nyköping Sweden
Örebro University Hospital Örebro Sweden
Södertälje sjukhus Södertälje Sweden
Södersjukhuset Stockholm Sweden
Sjukhuset Torsby Torsby Sweden
Västmanlands sjukhus Västerås Sweden

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04700969 on ClinicalTrials.gov ↗ ← All trials in Sweden