Bariatric Surgery
Conditions
Keywords
Bariatric surgery, video education, quality of recovery, surgical fear
Brief summary
The goal of this randomised clinical study is to is to determine the effect of video education given before bariatric surgery procedure on surgical fear and recovery. The main questions it aims to answer \[is/are\]: Video training reduces patients' fear of surgery. Video training improves the quality of recovery for patients. There is a comparison group: Researchers will compare the effect of the given video training to see if it has an impact on surgical fear levels and quality of recovery. In video group (Experiment group), patients will watch a video prepared by researchers before their surgery.
Interventions
OTHERVideo education
A preoperative information video specific to bariatric surgery has been prepared.
OTHERControl Group
Standart care
Sponsors
Bursa Sevket Yilmaz Training and Research Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 53 Years
Healthy volunteers
No
Inclusion criteria
* Individuals who have undergone bariatric surgery, * 18 years of age or older, * volunteer to participate in the study.
Exclusion criteria
* Patients who have previously undergone bariatric surgery, * who do not attend regular post-operative follow-up appointments, * who cannot be contacted by phone, * who have an American Society of Anesthesiologists (ASA) score of III or higher, and who have a psychiatric disorder.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Surgical fear | Patients completed the surgical fear scale twice: once two days before the surgery and once one day before. | It was used to determine the levels of fear in patients before surgery. |
| Quality of recovery | Patients' quality of recovery was assessed twice, on day 1 and day 7 post-surgery. | Quality of Recovery-15 (QoR-15): This scale evaluates five areas-emotional status, physical comfort, psychological support, physical independence, and pain-to assess patients' postoperative surgical recovery. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain | Patients' pain scores were recorded by the patients themselves a total of 3 times, on days 1, 3, and 7 postoperatively, in the mornings before taking analgesics. | Visual analog scale: It was used to measure the postoperative pain levels of patients. |
Countries
Turkey (Türkiye)
Outcome results
None listed