Diet workshop for improving protein intake after bariatric surgery
Evaluation of the Implementation of a Diet Workshop on the 15th Postoperative Day Following Bariatric Surgery on the Protein Intake of the Patient
This study tests whether a dietary workshop can help people who had bariatric surgery improve their protein intake for better recovery and health.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 88 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Clermont-Ferrand Academic / other |
| Locations | 1 site (Clermont-Ferrand) |
| Trial ID | NCT05695040 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a dietary workshop conducted on the 15th postoperative day for patients who have undergone bariatric surgery. The workshop focuses on enhancing protein intake, which is crucial for recovery and overall health post-surgery. Participants will be assessed on their ability to incorporate dietary recommendations into their recovery process. The study aims to determine if this intervention can lead to better nutritional outcomes for patients.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 scheduled for bariatric surgery, such as sleeve gastrectomy or bypass surgery.
Not a fit: Patients who follow a diet excluding animal proteins, such as vegetarians and vegans, may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve protein intake and nutritional recovery for patients after bariatric surgery.
How similar studies have performed: While specific similar studies were not mentioned, dietary interventions post-surgery have shown promise in improving recovery outcomes in other contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male or female * Over 18 years of age * Scheduled for bariatric surgery such as sleeve gastrectomy or bypass surgery. * Able to give informed consent to participate in the research. * Enrolled in a Social Security system. Exclusion Criteria: * Inability to travel to participate in the workshop. * Patients with a diet excluding animal proteins (vegetarians, vegans). * Pregnant and lactating women. * Inability to comply with protocol recommendations. * Incapacitated patients. * Major deprived of liberty * Refusal to participate.
Where this trial is running
Clermont-Ferrand
- CHU clermont-ferrand — Clermont-Ferrand, France (Recruiting)
Study contacts
- Principal investigator: Jessica RODA — University Hospital, Clermont-Ferrand
- Study coordinator: Lise Laclautre
- Email: promo_interne_drci@chu-clermontferrand.fr
- Phone: 334.73.754.963
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.