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Clinical Trials/NL-OMON49513
NL-OMON49513
Recruiting
Not Applicable

Direct measurement of changes in food intake behaviour in obese women after bariatric surgery or lifestyle intervention - CIBuS

Rijnstate Ziekenhuis0 sites24 target enrollmentTBD
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Conditionsobesitasmorbid obesityoverweight10003018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
obesitas
Sponsor
Rijnstate Ziekenhuis
Enrollment
24
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Rijnstate Ziekenhuis

Eligibility Criteria

Inclusion Criteria

  • •\- Age between 18 and 67 years of age (standard for eligibility for bariatric
  • •\- Patients must be able to adhere to the study visit schedule
  • •\- Independently mobile
  • •\- Patients must be able to give informed consent (IC) prior to any study
  • •\- Surgical (1\) and non\-surgical (2\) groups:
  • •1\. Eligible for bariatric surgery (BMI \> 35 kg/m2 and clinically indicated
  • •bariatric surgery operation in agreement with the IFSO criteria)
  • •2\. Patients with a BMI of 30\-40 kg/m2, who are planning to join the
  • •COOL\-lifestyle program

Exclusion Criteria

  • •Pre\-operatively/lifestyle group: Factors impairing ability to consume meal
  • •o Significant dysphagia
  • •o Gastric outlet obstruction
  • •o Anything factor that prevents subjects from drinking or eating a meal
  • •Post\-operatively: Factors impairing ability to consume meal such as
  • •o Significant and persistent surgical complications or
  • •o Anything that prevents subjects from drinking or eating a meal.
  • •Systemic or gastrointestinal condition which may affect food intake or
  • •preference (including diabetes mellitus)
  • •Pregnancy or lactation, or planning to get pregnant during the study period

Outcomes

Primary Outcomes

Not specified

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