NCT07872605Completed
Structured Perioperative Nursing Education and Short-Term Outcomes After Metabolic Bariatric Surgery
Structured Perioperative Nursing Education and Short-Term Outcomes After Metabolic Bariatric Surgery: A Nonrandomized, Temporally Allocated Controlled Study
Source: ClinicalTrials.gov · Last updated 13 Oct 2026
Brief summary (registry, in English)
This study evaluated whether a structured, nurse-led perioperative education program, supported by an illustrated Arabic booklet, is associated with better short-term outcomes in adults undergoing metabolic and bariatric surgery (MBS). The main outcome was eating behavior at 6 months after surgery. Other outcomes were knowledge about bariatric surgery, weight loss, quality of life, and recorded postoperative symptoms and events. Patients who received routine hospital care were compared with patients who received the structured education program.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 86 (actual)
- First submitted
- 5 Oct 2026
- Start date
- 1 May 2024
- Primary completion date
- 31 Aug 2025
- Lead sponsor
- General Committee of Teaching Hospitals and Institutes, Egypt
- Diseases
- Obesity
- NCT number
- NCT07872605
What you commit to
- Study type: Interventional
- Participants enrolled: 86
- From 1 May 2024 to the primary completion date, 31 Aug 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Age
- Age below 20 years or above 60 years
Other
- BMI of 35 kg/m² or lower
- Participation in the pilot study used to test the study questionnaires
Who the study is looking for
- Adults aged 20 to 60 years
- Body mass index (BMI) above 35 kg/m²
- Scheduled for any type of metabolic and bariatric surgery at the Experimental and Clinical Surgery Department, Medical Research Institute, Alexandria University
- Willing to participate and able to give written informed consent
Age in the registry: 20 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Medical Research Institute, Alexandria University Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.