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Methods: Forty patients will be allocated into two groups: laparoscopic (n = 20) or open surgery (n = 20).
In NEYNL, there are 150 trainees that will be allocated into 20 groups of 7-8 trainees.
Following surgery, patients will be allocated into study groups based on histological findings (Fig. 1): Group A: Patients whose tumours have no adverse histological features will not receive any adjuvant treatment as per standard of care.
The following baseline measures of outcome will be recorded: Numerical pain rating scale on a 0 10 scale [ 14]; A back specific disability scale (Roland Morris Disability Scale) [ 15]; A patient specific measure of disability (Patient Specific Functional Scale)[ 16]; Immediately after completing baseline measures participants will be allocated into treatment groups.
When the envelope contains a green card, the participant will be allocated into the experimental group.
When the envelope contains a red card, the participant will be allocated into the control group.
The 20 PHCCs will be allocated into intervention or control groups by using a stratified randomizing sequence by number of caregivers, generated by a computer (EPIDAT 3.1).
In this randomised, controlled multicentre study in general practice in Southern Norway, 270 patients will be allocated into one of two treatment groups, using a web-based application based on block randomisation.
Recruited practices will be allocated into intervention arms using block randomization.
Participants will be allocated to three groups according to the group number printed inside the envelopes.
Participants will be allocated to the group by the Study Coordinator, and will be aware of the allocated group.
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CEO of Professional Science Editing for Scientists @ prosciediting.com