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Clinical Trial Summary

The primary aim of this study is to examine the effects of in-bed rotation and early mobilization training given before abdominal surgery on mobility, pain and comfort of patients after surgery. The secondary aim of the study is to examine the effect of mobilization training given before abdominal surgery on the sleep of patients after surgery.


Clinical Trial Description

The primary aim of this clinical trial study is to examine the effects of early mobilization training given before abdominal surgery on mobility, pain and comfort of patients after surgery. The secondary aim of the study is to examine the effect of mobilization training given before abdominal surgery on the sleep of patients after surgery. Research Hypotheses are: H11. There is a difference between the mobility scores of the patients who were given and not given pre-abdominal surgery training. H12. There is a difference between the comfort scores of patients who were given and not given pre-abdominal surgery training. H13. There is a difference between the sleep scores of the patients who were given and not given pre-abdominal surgery training. First, the patient's mobility status in the preoperative period was evaluated with these scales. "Early Mobilization Training" will be given to the patients in the intervention group in the preoperative period. "Early Mobilization Training Material" to be prepared by the researcher will be used as training material. The training content will include information about the techniques and points to be considered about turning from one side to the other in the bed, sitting on the side of the bed, standing on the side of the bed and walking in the patient's room, and the time spent outside the bed on the day of surgery and the first and subsequent days after surgery. After the patient's mobilization on the first day after the operation, the Patient Mobility Scale, the Postoperative Mobilization, the Visual Analogue Scale (VAS) questions questioning the pain and comfort during lying and sitting, and sleep status will be filled. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05657561
Study type Interventional
Source Eastern Mediterranean University
Contact
Status Enrolling by invitation
Phase N/A
Start date February 2, 2022
Completion date December 31, 2023

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