Ariel University
Ariel, 40700, Israel
NCT Number: NCT06192537
A quasi-experimental design (i.e., "One-Group Pretest-Posttest Design") will be applied among 34 convenient samples of undergraduate students in their first year of nutrition sciences program at Ariel University and Tel-Hai College. The intervention will take place at the simulation centers of the institutions. All participants will be asked to wear an obesity simulation suit (Unisex obesity Simulation suit, Erler-Zimmer, Germany) and to participate in a standardized scenario that simulates meetings between a person with obesity and a 'registered dietitian'. The 'registered dietitian' will be presented by a professional role-player and the scenario will encompass different levels of weight bias. At baseline, 1- and 3-week post-intervention both groups will be asked to fill in a survey using "Qualtrics" software. The survey will include the Anti-Fat Attitudes questionnaire (AFA), the Short-Form of Fat-Phobia scale (F-scale), the Weight-Implicit Association-Test (weight-IAT), and the Jefferson Scale of Empathy. Data on demographics, weight history, and perception, measurement of actual weight and height, and the beliefs about the causes of obesity questionnaire will be collected at baseline.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Ariel, 40700, Israel
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All participants will be asked to wear an obesity simulation suit (Unisex obesity Simulation suit, Erler-Zimmer, Germany) and to participate in a standardized scenario that simulates meetings between a person with obesity and a 'registered dietitian'. The 'registered dietitian' will be presented by a professional role-player and the scenario will encompass different levels of weight bias through dialogue and the use of inappropriate equipment.
Time frame: Change from baseline at three- weeks post-intervention
The 'AFA' indicates explicit anti-fat attitudes toward people with obesity and is composed of 13-items rated on a 10-point Likert scale and divided into three subscales ('dislike', 'fear about fat' and 'willpower'), with higher total scores indicating stronger anti-fat attitudes.
Time frame: Change from baseline at three- weeks post-intervention
The 'F-scale' indicates fat-phobic attitudes toward people with obesity and is composed of 14-pairs of adjectives that are used to describe people with obesity (e.g., 'no willpower' vs. 'has willpower') and ranked on a 1-5 scale according to the point closest to the adjective name that describes their feelings and beliefs. Higher scores indicate stronger fat-phobic attitudes.
Time frame: Change from baseline at three- weeks post-intervention
IAT tool is an indirect measure of implicit bias toward weight which uses the constructs of "fat people" versus "thin people" and the polarized attitudes of "good" and "bad" to detect implicit weight bias.
Time frame: Change from baseline at three- weeks post-intervention
A 20-item scale that is designed to measure empathy in medical students.
Time frame: At baseline
Questions regarding age, gender, occupation, marital status, and religious affiliation.
Time frame: At baseline
Questions regarding self-definition of weight status, the importance of weight to self-confidence, and much control a person has over the weight.
Time frame: At baseline
Questions regarding obesity during childhood, obesity during last decade, family members who struggle with obesity, currently in any process of losing weight.
Time frame: At baseline
Measurement of actual weight in kilograms.
Time frame: At baseline
Measurement of actual height in meters.
Time frame: At baseline
Rating the importance of 20 factors contributing to obesity by using a 5-point Likert-scale response format.
Ariel University
Other
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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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