N/A
N=453
The Effect of A New Perioperative Practice Model on Patient, Nursing And Organisational Outcomes
Arthroplasties, Hip Replacement · Arthroplasties, Knee Replacement
Bottom Line
View on ClinicalTrials.gov: NCT02906033 ↗Enrolled (actual)
453
Serious AEs
—
Results posted
Dec 2021
Primary outcome: Primary: Change From Baseline to Follow-up in Health Related Quality of Life — 0.059; 0.055 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- New perioperative practice model (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Hospital District of Helsinki and Uusimaa
- Primary completion
- Dec 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change From Baseline to Follow-up in Health Related Quality of Life |
0.059; 0.055 | — |
| SECONDARY Change in Surgery-related STATE Anxiety From Baseline to Follow-up |
-4.91; -5.21 | — |
| SECONDARY Quality of Perioperative Care as Experienced by Surgical Patients |
4.85; 4.83; 4.95; 4.90; 4.61; 4.58 | — |
| SECONDARY Change in Surgery-related TRAIT Anxiety From Baseline to Follow-up |
-0.76; -2.05 | — |
Summary
The aim of the study is to improve the surgical patients' care process. The objective is to explore the effect of a new perioperative practice model on 1) patient outcomes (satisfaction, surgery-related anxiety and quality of life), 2) nursing outcomes (organizational engagement), and 3) organization outcomes (timeline of surgical care process).
Eligibility Criteria
Inclusion Criteria
- the patient has been scheduled for a primary elective hip or a knee replacement procedure under spinal anesthesia
- the patient is 18 years of age or older
- the patient is able to participate in the study either in Finnish or Swedish
- the patient is able to give his/her written consent to participate the study
- the patient is willing to participate the study
- the patients operation time is scheduled on Monday through Thursday in the operating department K in the Peijas hospital
Exclusion Criteria
- None
Data sourced from ClinicalTrials.gov (NCT02906033). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.