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临床试验/NCT05929469
NCT05929469已完成不适用

PATH to Health: An Exploration of Digital Behavioral Weight Loss Approaches

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 99 人开始时间: 2023年10月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
99
试验地点
2
主要终点
Feasibility- Rate of early nonresponse

研究概览

简要总结

The purpose of this initial pilot and feasibility study is to test different digital, behavioral weight loss approaches, with or without human support, using a sequential, multiple assignment, randomized trial (SMART) design. All participants in this pilot trial will receive a 3-month mobile health (mHealth) program. The dose of human support will vary by first- and second-line randomizations. The feasibility, acceptability, and preliminary outcomes for each of the treatment sequences will be assessed.

详细描述

Ninety-nine adults, ages 18-65, with overweight or obesity, will be randomized in total. All participants will receive an mHealth program (App) for program duration that includes activity tracking with a Fitbit, weight tracking with a smart scale, and an app for diet tracking. At baseline, participants will be randomized to either a a) Fully Automated Kick-Off, or b) Human-Enhanced Kick-Off. "Early responders" will continue with to use App, alone. After 4 weeks, "early non-responders" in both arms will be re-randomized once to one of two augmented interventions with human support: Counseling or Check-In. Assessments will occur at baseline, 1 week, 4 weeks, and 3 months to explore feasibility, acceptability, and preliminary outcomes (weight, self-monitoring adherence, behavioral goal adherence).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Current age: 18-65 years
  • Lives in North Carolina
  • Body mass index (BMI) of 27.5-45 kg/m^2
  • Ability to read, write, and speak English
  • Ownership of iPhone with a data and texting plan
  • Ability to commit to the required counseling sessions (0-5 sessions, based on randomization)
  • Is not living a participant or staff member on this trial
  • Willingness to be randomized to any of the treatment sequences

排除标准

  • Weight loss of more than 10 pounds in the last 6 months that was maintained
  • A history of weight loss surgery
  • Pre-existing medical condition(s) that prevent them from adhering to a supervised exercise routine
  • Have Type 1 Diabetes or are currently taking medicine for Type 2 Diabetes
  • Have recently been diagnosed or treated for cancer
  • Currently pregnant, pregnant within the past 6 months, or plan to become pregnant in the next 6 months
  • Report taking prescription or over the counter medication with a known impact on metabolism or weight
  • Report a history of an eating disorder
  • History of psychotic disorder or bipolar disorder, or have been hospitalized for depression or other psychiatric disorder within the past 12 months
  • History of alcohol or substance abuse
  • Current participation in another weight loss program that may interfere with participation in this study

结局指标

主要结局

Feasibility- Rate of early nonresponse

时间窗: 4 weeks

The rate of early response will be calculated as the number of individuals deemed "early responders" divided by the total number of participants randomized.

Feasibility- Percentage of participants with missing data at 4 weeks

时间窗: 4 weeks

The percentage of participants with missing data at 4 weeks will be calculated as the number of participants who do not complete the 4-week weight assessment divided by the total number of participants randomized.

次要结局

  • Weighing Self-Monitoring Adherence(Baseline to 3 months (daily))
  • Dietary Self-Monitoring Adherence(Baseline to 3 months (daily))
  • Change in Physical Activity(Baseline, 3 months)
  • Change in Diet(Baseline, 3 months)
  • Acceptability- Rate of attendance at human support sessions(Up to 3 months)
  • Weight Change- Percent weight change from baseline to 3 months(Baseline, 3 months)
  • Weight Change- Percent weight change from 4 weeks to 3 months(4 weeks, 3 months)
  • Acceptability- Overall program satisfaction rating(3 months)
  • Activity Goal Adherence(Baseline to 3 months (daily))
  • Weight Change- Percent weight change from baseline to 4 weeks(Baseline, 4 weeks)
  • Acceptability- Attrition(Up to 3 months)
  • Physical Activity Self-Monitoring Adherence(Baseline to 3 months (daily))
  • Dietary Goal Adherence(Baseline to 3 months (daily))
  • Change in Motivation(Baseline, 1 week, 4 weeks, 3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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