The Effect of Progressive Relaxation Exercises on Bariatric Surgery Period (PREbari)
Obesity, Morbid, Bariatric Surgery Candidate, Anxiety
About this trial
This is an interventional prevention trial for Obesity, Morbid focused on measuring bariatric surgery, Progressive relaxation exercises, anxiety, postoperative pain
Eligibility Criteria
Inclusion Criteria:
- Having bariatric surgery plan (such as sleeve gastrectomy, gastric bypass),
- 18 years and over,
- Do not have any medically diagnosed health problems (neurological, psychiatric, orthopedic) that will prevent learning and practicing progressive muscle relaxation exercises,
- Agreeing to apply progressive relaxation exercises, willing and willing to participate in the study,
- Patients who do not know and practice progressive relaxation exercises before will be included in the study.
Exclusion Criteria:
- Patients younger than 18 and older than 65,
- Patients who do not want to apply progressive relaxation exercises,
- who do not apply them as desired during the study period,
- who have health problems (neurological, psychiatric, orthopedic) that may affect their ability to do the exercises will be excluded from the study.
Sites / Locations
- Başakşehir Çam & Sakura Şehir Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Progressive relaxation exercises group
Control group
Participants will be randomly selected by a computer based system (Block randomization was used to keep the sample size of the groups similar. Random Allocation Software (Ver. 1.0.0) will be used to allocate the patients to groups). Selected participants will be invited to a meeting which will be held face-to-face and in a quiet environment. Progressive Relaxation Exercises will be explained to this group in a step-by-step manner whose surgery date is determined to undergo bariatric surgery by the relevant researcher. After this stage, participants will be followed to do the exercises regularly for a month by a researcher. Patients will fill the Amsterdam Preoperative Anxiety and Information Score Scale preoperatively at the hospital. After the surgery, the patients will be evaluated by the researchers in terms of pain scores and analgesic usage frequency in the recovery room and 1st, 4th, 8th, 12th, 24th, 36th and 48th hours data will be collected in the postoperative service.
This group will be the randomized selected patients who will not get any intervention. Patients will fill the Amsterdam Preoperative Anxiety and Information Score Scale preoperatively at the hospital. After the surgery, the patients will be evaluated by the researchers in terms of pain scores and analgesic usage frequency in the recovery room and 1st, 4th, 8th, 12th, 24th, 36th and 48th hours data will be collected in the postoperative service.