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Completed

NCT Number: NCT06480058

Predictors of Bariatric Surgery Weight Loss

The aim of the observational cross-sectional study is to determine the prevalence and correlates of disordered eating among candidates for bariatric surgery in the BariPredict cohort.

The study aims to answer the following question on whether the prevalence of disordered eating is higher in individuals that are candidates of bariatric surgery compared to the general population with obesity.

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Key information

About this study

Participants referred to Jaber Al Ahmad Al Sabah Hospital, Hawalli, Kuwait, for bariatric surgery were consecutively screened for the study.

A cross-sectional analysis was performed on a subgroup of this cohort with complete baseline data. The analysis investigates the influence of psychological factors associated with obesity before bariatric surgery.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Obesity BMI > 30 kg/m2
  • 18 years and older

Exclusion criteria

  • BMI < 30 kg/m2

Treatment and study plan

Primary outcomes

  1. Eating Disorder Screening

    Time frame: 1 Day

    A validated SCOFF questionnaire will be self-administered to patients attending their first preoperative bariatric surgery appointment. The SCOFF questionnaire is a simple 5-question test developed to assess the possible presence of an eating disorder. The S in SCOFF stands for "sick" (to vomit). The O stands for "one stone" of weight (i.e., 6.35 kg). The letters C, F and F stand for "control", "fat" and "food" respectively. Although the SCOFF is not used for diagnostic purposes, a score of 2 or more positive answers raises the index of suspicion of eating disorders, highlighting the need for a more detailed psychological history .The SCOFF has been previously validated in Arab populations.

Secondary outcomes

  1. Anxiety

    Time frame: 1 Day

    Kuwait University Anxiety Scale (KUAS)

    The Kuwait University Anxiety Scale will be used to measure level of anxiety. The 20-item scale will capture cognitive/affective anxiety (9 items), subjective anxiety or nervousness (7 items), and somatic anxiety (4 items) [4]. Responses use a 4-point Likert scale ranging from 1=rare, 2=sometimes, 3= often, 4= always to measure the level of anxiety . The cut offs to indicate anxiety include 0 - 21 normal, 22 - 42 mild anxiety, 42 - 63 moderate anxiety, 64 - 84 severe anxiety.

  2. Depression

    Time frame: 1 Day

    Beck Inventory

    Psychological screening and assessment for anxiety and depression will be carried by a clinical psychologist using a validated questionnaire. The Beck Depression inventory which includes a 21-item multiple choice self-report inventory will be used to measure depressive symptoms within the last week. Each question includes a set of 4 possible choices of how a participant may feel. Choices are scored from 0 to 3, increasing in intensity. The cut-offs to indicate depression include 0 - 9 minimal depression, 10 - 18 mild depression, 19 - 29 moderate depression, 30 - 63 severe depression.

  3. Obesity

    Time frame: 1 Day

    Height and weight will be measured using standard protocols by a qualified nurse during the patient's preoperative and post-operative appointments. Body Mass Index (BMI) will be calculated using WHO cut-off points to define obesity. Obese patients will be divided into different classes of obesity as the following: obese class I (BMI 30 - 34.9 kg/m2), obese class II (35 - 39.9 kg/m2) and obese class III (BMI > 40 kg/m2).

Sponsors and collaborators

Lead sponsor

Kuwait University

Other

Collaborators

  • Dasman Diabetes Institute
  • Jaber Al Ahmad Al Sabah Hospital

Registry information

Official study title

Determinants of Eating Disorder Risk in Pre-intervention Bariatric Surgery Candidates.

Acronym: BariPredict

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jun 28, 2024
Registry last updated
Jun 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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