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临床试验/NCT03845283
NCT03845283进行中(未招募)不适用

Optimization and Evaluation of a Tailored Behavioral eHealth/mHealth Weight Loss Intervention for Cardiac Rehabilitation Patients Using the Multiphase Optimization Strategy

The Miriam Hospital2 个研究点 分布在 1 个国家目标入组 198 人开始时间: 2019年5月2日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
198
试验地点
2
主要终点
Weight Change

研究概览

简要总结

Cardiovascular disease (CVD) is the leading cause of death in the United States. Cardiac rehabilitation (CR) is the main treatment for heart attacks and other types of CVD. It is based on science, it saves money, and it is widely-available. Each session (of which there are a few each week for 3 months) combines supervised exercise and instruction. The goals are to improve overall health and reduce cardiovascular risk in individuals with established CVD. CR produces almost no weight loss (WL); if a person has excess weight while in CR (the majority of participants have overweight or obesity), losing weight could really reduce their risk of having another heart attack. The best treatment available for weight loss, in-person behavioral weight loss interventions (BWLs), produce enough WL that they improve health and disease risk/severity. However, in-person BWLs are too much work to be carried out in CR. A previous fully automated 3-month online program, Rx Weight Loss (RxWL), produced good WL in many different settings. Dr. Goldstein aims to tailor RxWL for use in CR. The study will use the Multiphase Optimization Strategy (MOST) to test innovative eHealth/mHealth intervention components that might work well for people when combined with RxWL. The study will include 160 patients (each randomized to receive 0-4 of the components). The components are: (a) a Fitbit with a goal-setting program; (b) a bite counting device; (c) a Web-based virtual reality (VR) intervention ; and (d) virtual meetings. By the 6-month follow-up, the investigators will know if any of those 4 components helped people lose more weight. If a component produced at least 2% WL, it will be studied further by being included in a new intervention to be tested in the next study.

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
Single (Outcomes Assessor)

入排标准

年龄范围
21 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • currently a participant in The Miriam Hospital's or Newport Hospital's outpatient phase II cardiac rehabilitation program
  • medical clearance to participate by the Medical Director
  • a body mass index (BMI) between 27-45 kg/m2
  • must have a personal computer in their home with internet access
  • must read and understand English
  • willing to use technology to assist with weight loss

排除标准

  • currently in another weight loss program
  • taking weight loss medication
  • weight loss of ≥ 5% of body weight in the past 6 months
  • currently pregnant, lactating, < 6 months post-partum, or plans to become pregnant during the next year
  • report of loss of consciousness on the Physical Activity Readiness Questionnaire
  • New York Heart Association Class IV heart failure
  • heart transplant in the last 3 months
  • receipt of left ventricular assist device in the last 2 months
  • a physician diagnosis of dementia
  • a physician prescription for 24 hours of oxygen therapy daily
  • coronary artery bypass surgery in the last 4 weeks
  • current participation in dialysis
  • inability to walk 1 block without stopping
  • report of conditions that in the opinion of the investigators would render them potentially unlikely to follow the protocol including terminal illness, substance abuse, eating disorder, or other significant psychiatric problems

结局指标

主要结局

Weight Change

时间窗: At baseline, 3-, and 6-months after initiating the program

The difference between initial weight and weight at the follow-up assessments. Patients will be asked to step on a scale at the assessment clinic.

次要结局

  • Structured Weekly Moderate-to-Vigorous Physical Activity Minutes(At baseline, 3-, and 6-months after initiating the program)
  • Number of Bites(At baseline, 3-, and 6-months after initiating the program)
  • Weight Control Practices(At baseline, 3-, and 6-months after initiating the program)
  • Weight Loss Self-Efficacy: Weight Efficacy Lifestyle Questionnaire(At baseline, 3-, and 6-months after initiating the program)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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