跳至主要内容
临床试验/NCT06044285
NCT06044285招募中不适用

Ultra Crave: A Biopsychobehavioral Investigation of Withdrawal From Ultra-Processed Food in Humans

University of Michigan2 个研究点 分布在 1 个国家目标入组 210 人开始时间: 2023年8月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
210
试验地点
2
主要终点
Craving of ultra-processed (UP) foods

研究概览

简要总结

This study experimentally investigates whether a reduction in ultra-processed (UP) food intake (1) causes aversive withdrawal symptoms in humans, (2) increases the motivational salience of UP food cues and, if so, (3) whether these factors undermine the ability to adhere to a low-UP diet. The following aims and hypotheses are tested:

Aim 1: To investigate whether aversive physical, cognitive, and affective withdrawal symptoms emerge in response to reduced UP food intake compared to a high-UP diet, and whether this predicts failure to adhere to a low-UP diet.

H1a: Reducing UP food intake will result in aversive physical, cognitive, and affective withdrawal symptoms, as indicated by 1) ecological momentary assessment (EMA) reports of aversive withdrawal symptoms, and 2) heart rate reactivity and subjective distress to an in-lab stressor.

H1b: Aversive symptoms of UP food withdrawal will predict greater UP food intake and higher blood glucose levels when trying to adhere to a low UP diet.

Aim 2: To investigate whether increased motivational salience of UP food cues emerges in response to reduced UP food intake, and whether this predicts failure to maintain a low-UP diet.

H2a: Reducing UP food intake will result in increased motivational salience of UP food cues, as indicated by 1) EMA reports of UP food craving, 2) heart rate reactivity and subjective craving in a simulated fast-food restaurant, 3) heightened reinforcement value for UP food relative to other reinforcers, and 4) greater reward-related neural response to UP food cues.

H2b: Increased motivational salience of UP food cues will predict greater UP food intake and higher blood glucose levels when trying to adhere to a low UP diet.

详细描述

The study will include a combination of in-person, at-home, and virtual activities over the course of ~14 days (contingent on scheduling, this duration may vary and particularly between in-person visits #1 and #2). Participants complete three in-lab visits. Visit 1 and 2 will each followed by a week of remote data tasks (e.g., EMA, continuous glucose monitoring, physical activity and sleep tracking (Fitbit), and two 24-hour dietary recall interviews).

During in-lab visit #1, participants will complete questionnaires, behavioral tasks, and interviews, and will have body composition measurements taken (height, weight, Inbody scan). Participants will complete the remote tasks for the following week while eating their typical diet (i.e., baseline period).

During in-lab visit #2, participants will complete questionnaires, interviews, and body composition measurements (height, weight, Inbody scan). Participants are randomly assigned to one of three conditions--control (i.e., high UP), self-guided low UP, or meals provided low UP--and will follow instructions about how to eat consistent with their condition during week 2 of remote data collection (i.e., dietary intervention period).

During in-lab visit #3, participants will complete questionnaires, behavioral tasks, body composition measurements (height, weight, InBody scan), and an fMRI scan.

Participants are contacted 1- and 3-months later to complete a short follow-up survey and provide information about their current diet.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Participants and outcome assessors will be blinded to the participants' condition. The study coordinator will oversee the randomization protocol.

入排标准

年龄范围
22 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 22 to 60 years of age
  • English-speaking
  • Must own an Android or iPhone Smartphone
  • Live within a 1-hour radius of the laboratory
  • endorsement of > 4 symptoms on the YFAS 2.0 completed during eligibility screener; at the time of consent, symptom count must remain above threshold for food addiction (this discrepany is based on a previously found tendency during pilot testing to overestimate food addiction symptoms at the time of screening)
  • Willing and able to follow specific dietary instructions provided by the study team
  • Willing and able to attend 3 in-person lab visits
  • Willing to complete 4 phone interviews about foods eaten in the past 24 hours
  • Willing to report daily intake of food
  • Like the taste of chocolate milkshake (for fMRI scan eligibility only).

排除标准

  • participants with a self-reported BMI < 18.5 and > 40
  • Current diagnosis of disorder that may impact study results or the ability to safely complete study tasks (hypothyroidism (uncontrolled by medication), diabetes, etc.)
  • History of food allergies
  • Unable to respond to brief questionnaires within 90-minutes during the day
  • Work night shifts or irregular shifts
  • Restrictive dietary requirements (e.g., vegan) or high levels of picky eating
  • Medications (e.g., insulin, antipsychotic medications) that may impact study results or safe completion of study tasks
  • Diagnosis of severe mental illness (e.g., schizophrenia, bipolar disorder)
  • Diagnosis of a restrictive eating disorder (e.g., Anorexia Nervosa, Bulimia Nervosa, purging disorder) within the last 5 years
  • Current diagnoses of disorders that can impact reward/metabolic functioning
  • 20+ pound weight fluctuation in the last 3-months
  • Prior weight loss surgery (e.g., bariatric surgery)
  • Currently pregnant, breastfeeding, trying to get pregnant, or within 6-months of having given birth
  • High levels or high-risk intake of alcohol or caffeine
  • Use of tobacco or nicotine in the past month
  • Use of THC cannabis within the past week
  • Unwillingness to abstain from THC cannabis, tobacco or nicotine during the main portion of the study (~22 days)
  • fMRI contraindications (e.g., claustrophobia, metal implants).
  • inability to complete a random report within 90 minutes

研究组 & 干预措施

Meals Provided Low UP Food Diet

Experimental

.Participants asked to eat a low UP food diet provided by the study team.

干预措施: Low UP (meals provided) (Other)

Control

Active Comparator

Participants asked to eat as they usually do.

干预措施: Active Control (Other)

Self-Guided Low UP Food Diet

Experimental

Participants asked to eat a low UP food diet according to study provided nutritional guidance.

干预措施: Low UP (self-guided) (Other)

结局指标

主要结局

Craving of ultra-processed (UP) foods

时间窗: Assessed during dietary intervention period for 1 week

Craving of UP foods will be assessed using EMA on a scale from 1 (not at all) to 7 (extremely); higher scores indicate greater craving of UP foods.

Withdrawal Symptoms

时间窗: Assessed during dietary intervention period for 1 week

Withdrawal symptoms (e.g., anger, anxiety) will be assessed using ecological momentary assessment (EMA) on a scale from 1 (not at all) to 7 (extremely); higher scores indicate greater withdrawal symptoms.

Low UP food intake

时间窗: Assessed during dietary intervention period for 1 week

Intake of low UP foods will be assessed using two 24 hour dietary recall interviews.

Self-Reported Low UP food intake

时间窗: Assessed during dietary intervention period for 1 week

Intake of low UP foods will be assessed using EMA reports of food intake. Responses will be coded into high and low UP food intake based on the NOVA classification.

次要结局

  • Reactivity to a stressor(Assessed post-dietary intervention during in-lab Visit 3 (1 day))
  • Self-reported reactivity to a stressor(Assessed post-dietary intervention during in-lab Visit 3 (1 day))
  • Self-reported cue reactivity to a simulated fast food restaurant(Assessed post-dietary intervention during in-lab Visit 3 (1 day))
  • Level of reinforcement value for ultra processed foods(Baseline assessed during in-lab Visit 1 (1 day); assessed again post-dietary intervention during in-lab Visit 3 (1 day))
  • Cue reactivity to a simulated fast food restaurant(Assessed post-dietary intervention during in-lab Visit 3 (1 day))
  • Magnitude of neural reward-related response to tasting a milkshake(Assessed post-dietary intervention during in-lab Visit 3 (1 day))
  • Blood Glucose Level(Assessed during dietary intervention period for 1 week)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ashley Gearhardt

Associate Professor of Psychology, College of Literature, Science, and the Arts

University of Michigan

研究点 (2)

Loading locations...

相似试验