The Effect of Pain Education on Pain and Comfort
Pain, Postoperative
About this trial
This is an interventional prevention trial for Pain, Postoperative focused on measuring Anorectal diseases, pain, confort, Pain education
Eligibility Criteria
Inclusion Criteria: - Being over 18 years old, literate, having surgery for anorectal diseases, having surgery under spinal anesthesia and volunteering to participate in the research. Exclusion Criteria: using analgesia, mentally ill
Sites / Locations
- Home
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
experimental group
control group
A 'Patient Pain Education Brochure', which was prepared the day before the surgery, was given, and at the same time, the training was given verbally and in writing for an average of 20-30 minutes in the patient's own room. Vital sessions and pain assessment were performed during admission to the ward before the training. Pain was evaluated together with the patient's vital signs at the 15th, 30th, 45th, 60th minutes, 2nd, 4th, 6th, 12th, and 24th hours after the surgery. Comfort assessment was performed at the 24th hour after surgery.
One day before the operation, vital signs and pain were evaluated during hospitalization. Pain was evaluated together with the patient's vital signs at the 15th, 30th, 45th, 60th minutes, 2nd, 4th, 6th, 12th, and 24th hours after the surgery. Comfort assessment was performed at the 24th hour after surgery.