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Clinical Trials/NCT05695040
NCT05695040RecruitingNot Applicable

Evaluation of the Implementation of a Diet Workshop on the 15th Postoperative Day Following Bariatric Surgery on the Protein Intake of the Patient

University Hospital, Clermont-Ferrand1 site in 1 country88 target enrollmentStarted: December 8, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
88
Locations
1
Primary Endpoint
Protein intake

Study Overview

Brief Summary

The objective of the study was to improve protein intake after the implementation of a dietary workshop performed on the 15th postoperative day following bariatric surgery.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Outcomes

Primary Outcomes

Protein intake

Time Frame: 1, 3, 6, and 12 months

Different measurements of protein intake will be performed at 1, 3, 6, and 12 months in order to observe an improvement in the kinetics of protein intake, the objective being to increase protein intake in the year following surgery and not only at a specific time.

Secondary Outcomes

  • Qualitative evaluation of the workshop at 12 months(12 months)
  • Patient's biometric parameters. Muscle function The patient's muscle mass. Undernutrition Nitrogen balance (ancillary ) Medico-economic evaluation(3, 6 and 12 months)

Investigators

Sponsor
University Hospital, Clermont-Ferrand
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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