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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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11 January 2021 |
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Main ID: |
NCT02906033 |
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Date of registration:
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09/09/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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The Effect of A New Perioperative Practice Model on Patient, Nursing And Organisational Outcomes
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Scientific title:
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The Effect of A New Perioperative Practice Model on Patient, Nursing And Organisational Outcomes |
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Date of first enrolment:
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September 12, 2016 |
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Target sample size:
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490 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02906033 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Health Services Research. Masking: Single (Participant).
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Phase:
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N/A
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Countries of recruitment
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Finland
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Contacts
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Name:
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Kristiina Junttila, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Hospital District of Helsinki and Uusimaa |
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Key inclusion & exclusion criteria
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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
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Arthroplasties, Knee Replacement
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Arthroplasties, Hip Replacement
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Intervention(s)
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Other: New perioperative practice model
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Primary Outcome(s)
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Change from baseline Health Related Quality of Life at three months after the surgical procedure
[Time Frame: Baseline 2-3 weeks prior to, and post-measurement 3 months after the procedure]
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Secondary Outcome(s)
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Quality of perioperative care as experienced by surgical patients
[Time Frame: On average the third postoperative day, depending the time of discharge]
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Change from baseline Surgery-related anxiety at three months after the surgical procedure
[Time Frame: Baseline 2-3 weeks prior to, and post-measurement 3 months after the procedure]
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Secondary ID(s)
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TYH2014211
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U1111-1185-9612
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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