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临床试验/NCT07430891
NCT07430891已完成不适用

Effects of Exercise-Based Obesity Simulation on Weight Bias and Clinical Decision-Making in Health Professions Students: A Randomized Controlled Trial

University of Wisconsin, River Falls1 个研究点 分布在 1 个国家目标入组 107 人开始时间: 2024年2月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
107
试验地点
1
主要终点
Change in Implicit Weight Bias

研究概览

简要总结

This study examines whether an exercise-based simulation can reduce weight bias and improve professional skills among health professions students. Weight stigma in healthcare settings can negatively affect patient communication, clinical decision-making, and patient engagement in health-promoting behaviors.

In this randomized controlled trial, undergraduate health professions students were assigned to one of three groups: (1) a control group completing a communication module and light stretching, (2) an exercise-only group completing treadmill walking, or (3) an exercise group completing treadmill walking while wearing an obesity simulation suit designed to represent additional body weight. The simulation aimed to provide students with an experiential understanding of movement challenges associated with higher body weight.

Participants completed assessments at baseline, one week, and eight weeks after the intervention. Outcomes included measures of implicit and explicit weight bias, empathy, clinical decision-making using patient scenarios, professional behavioral intentions, and reflective learning.

The purpose of this study is to determine whether a brief experiential intervention can reduce weight bias and improve competencies related to patient-centered and weight-inclusive care in health professions education.

详细描述

This randomized controlled trial evaluated the impact of an exercise-based obesity simulation on weight bias and professional competencies among undergraduate health professions students.

Participants (N = 107) were randomized in a 1:1:1 ratio to one of three conditions: (1) control (professional communication module and low-intensity stretching), (2) moderate-intensity treadmill exercise without simulation, or (3) treadmill exercise while wearing an adjustable obesity simulation suit representing approximately 20% additional body mass. The intervention consisted of a single 30-minute session.

Outcomes were assessed at baseline, 1-week follow-up, and 8-week follow-up. The primary outcome was change in implicit weight bias measured using the Weight Implicit Association Test. Secondary outcomes included explicit weight bias (Anti-Fat Attitudes Questionnaire; Fat Phobia Scale), empathy (Jefferson Scale of Empathy - Health Professions Student version), clinical decision-making using structured patient vignettes, behavioral intentions toward future patients, and structured reflective learning.

Physiological and perceptual responses during the intervention (heart rate, perceived exertion, discomfort, and affective valence) were also recorded to examine associations between experiential intensity and learning outcomes.

The study aims to evaluate whether a brief experiential educational intervention can reduce weight bias and improve empathy and clinical reasoning relevant to weight-inclusive care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Undergraduate student enrolled at the University of Wisconsin-River Falls in a health professions-related program or major
  • Age 18 years or older
  • Able to safely participate in moderate-intensity treadmill walking
  • Cleared to participate based on the American College of Sports Medicine (ACSM) preparticipation screening algorithm
  • Willing and able to provide informed consent and complete study assessments at baseline, 1-week, and 8-week follow-up

排除标准

  • Contraindications to exercise or treadmill walking based on ACSM screening (e.g., symptoms suggestive of cardiovascular, metabolic, or renal disease without medical clearance)
  • Current or past eating disorder (self-reported)
  • Body dysmorphic disorder (self-reported)
  • Recent weight-related trauma within the past 12 months (self-reported)
  • Any condition or injury that would make treadmill walking unsafe, as determined during screening

研究组 & 干预措施

Control

Active Comparator

Participants completed a time-matched session consisting of a 10-minute professional communication micro-module (etiquette, active listening, teamwork; no obesity-related content) followed by approximately 20 minutes of low-intensity stretching. The session was designed to control for instructor attention and time without exposure to exercise or obesity simulation.

干预措施: Control (Behavioral)

Exercise-only

Active Comparator

Participants completed a 30-minute treadmill walking session consisting of a 5-minute warm-up (2.5 mph, 0% grade), 20-minute walk (2.5 mph, 6% grade), and 5-minute cool-down. Heart rate and perceived exertion were monitored to ensure moderate-intensity exercise.

干预措施: Exercise-only (Behavioral)

Exercise with Obesity Simulation Suit

Experimental

Participants completed the same 30-minute treadmill protocol as the exercise-only group while wearing an adjustable obesity simulation suit. The suit added approximately 20% of body mass to simulate increased body weight and movement constraints during exercise.

干预措施: Exercise with Obesity Simulation Suit (Behavioral)

结局指标

主要结局

Change in Implicit Weight Bias

时间窗: Baseline, 1-week, and 8 weeks post-intervention

Implicit weight bias was assessed using the Weight Implicit Association Test (IAT). D-scores reflect the strength of automatic pro-thin/anti-fat associations. Higher positive scores indicate stronger implicit anti-fat bias. The primary outcome is the change in IAT D-score from baseline to 8-week follow-up.

次要结局

  • Explicit Weight Bias(Baseline, 1 week, and 8 weeks post-intervention)
  • Empathy Toward Patients(Baseline, 1 week, and 8 weeks post-intervention)
  • Clinical Decision-Making Quality(Baseline, 1 week, and 8 weeks post-intervention)
  • Reflective Learning Quality(1 week post-intervention only)

研究者

发起方
University of Wisconsin, River Falls
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gregory Ruegsegger

Professor

University of Wisconsin, River Falls

研究点 (1)

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