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临床试验/NCT07225426
NCT07225426进行中(未招募)不适用

Log2LoseAI: Reinforcement Learning to Create a Framework for Personalizing Financial Incentives

University of Utah1 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2026年2月4日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
94
试验地点
1
主要终点
Retention for outcomes

研究概览

简要总结

The purpose of this study is to determine the feasibility of providing personalized incentives for dietary self-monitoring and/or interim weight loss to people enrolled in a weight-loss program

详细描述

In this study, community outpatients will participate in a clinician-facilitated, group-based behavioral weight-loss program for 24 weeks. Dietary self-monitoring data (input by patients via a mobile phone dietary application) and weight data (input by patients via cellular scale) will be collected by a software platform. A reinforcement learning algorithm will use data collected during the trial to predict which participants will respond to a financial incentive. Incentives will be provided to participants predicted to respond, and they will be notified of incentives via text messaging.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Willing to attend virtual baseline and follow-up data collection visits
  • At least 18 years of age
  • Verified obesity as defined as a BMI ≥30 kg/m2
  • Agree to attend 13 biweekly group classes (virtual) delivered by a registered dietitian
  • Agree to review study materials between classes
  • Regular access to an unshared smart phone
  • Reliable access to internet
  • Able to speak and read English
  • Desire to lose weight
  • Able to connect to a video conference call using a smartphone, tablet or computer with a webcam and microphone
  • Ability to download and use Fitbit app daily
  • Have or be willing to create a Gmail address
  • Physical ability to stand on a scale without support

排除标准

  • Weight loss of at least 10lbs in the month prior to screening
  • Weight > 380lbs
  • Currently enrolled or enrolled in the previous month in a clinical, research, or community program focusing on lifestyle change that could affect weight
  • New user of weight loss medication
  • Pregnant, lactating or planning on becoming pregnant during the study
  • History of bariatric procedure or planning to have bariatric procedure in the study timeframe
  • Residing in a nursing home, skilled nursing facility or assisted living facility
  • Impaired hearing
  • Significant dementia, drug or alcohol abuse, or unstable psychiatric illness (e.g., schizophrenia, psychosis)
  • Current treatment for cancer or being treated for cancer (besides basal cell carcinoma or squamous cell) in the last 6 months
  • Use of insulin, sulfonylureas, or meglitinides due to increased risk for hypoglycemia
  • Diuretic medication doses higher than hydrochlorothiazide or chlorthalidone 25 mg daily, furosemide 40 mg daily, torsemide 20 mg daily, bumetanide 1 mg daily, or any use of metolazone; use of potassium-sparing diuretics is acceptable
  • Unstable heart disease in the 6 months prior to screening
  • Chronic kidney disease at stage 4 or higher
  • Exertional chest pain
  • Pain, fainting, or other conditions that prohibit mild/moderate exercise
  • History of ascites requiring paracentesis
  • Inducing vomiting to prevent weight gain or counteract the effects of eating an average of 1 time per week or more in the past 3 months*
  • Not suitable for study participation due to other reasons at the discretion of the investigators

研究组 & 干预措施

Personalized incentives

Experimental

Participants may receive financial incentives for weight loss if their performance suggests they respond to financial incentives.

干预措施: personalized financial incentives (Behavioral)

结局指标

主要结局

Retention for outcomes

时间窗: 25 weeks

number of participants who provide a weight at 25 weeks/number of participants who provide a baseline weight for the intervention

Screening-to-enrollment ratio

时间窗: Week 0

number of potential participants screened for the study/ number of participants who provide a baseline weight for the intervention

次要结局

  • Adherence to calorie logging(24 weeks)
  • Adherence to self-weighing(24 weeks)
  • Body weight(baseline to 25 weeks)

研究者

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

Corrine Voils

Professor

University of Utah

研究点 (1)

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