Feasibility of Using Smart Scales for Weight Gain Prevention in African American Breast Cancer Survivors: a Randomized Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 35
- 试验地点
- 2
- 主要终点
- Proportion of participants with completed assessments at 6 months
研究概览
简要总结
The purpose of this study is to test the feasibility of two 6-month behavioral interventions for weight gain prevention (self-regulation plus activity monitoring or self-regulation) among African American breast cancer survivors along with a delayed control group. Participants will be 45 African American post-treatment breast cancer survivors. Intervention content will be delivered online with one face-to-face individual meeting. Weight, clinical and psychosocial measures will be assessed at baseline, 3 and 6 months. It is hypothesized that it is feasible to deliver the two weight gain prevention interventions among African American breast cancer survivors, and participants in the two intervention groups will have a lower magnitude of weight gain at 6-month follow-up relative to those in the delayed control group.
详细描述
Breast cancer is the most commonly diagnosed cancer among African American women in the United States, and in North Carolina (NC), African American women are more likely to die from breast cancer compared to women of other races/ethnicities. Given this disparity and with approximately 90,000 African American breast cancer survivors in NC, it is important to identify modifiable factors that can help improve survival among this population. Behavioral interventions that promote weight management among breast cancer survivors can help reduce risks for prevalent comorbidities, such as cardiovascular disease and diabetes, and potentially improve prognosis and survival. While lifestyle interventions have shown promise in improving body weight in breast cancer survivors, none have focused on weight gain prevention in African American breast cancer survivors, nor evaluated the use of frequent self-weighing as a self-regulation strategy.
Regular self-weighing has been effectively used as an approach for weight maintenance that helps individuals monitor daily weight fluctuations and make small changes in energy balance behaviors. Given that the frequency of self-weighing among breast cancer survivors is unknown, and the importance of self-regulation behaviors for weight maintenance is well established, extending previous work to prevent weight gain among breast cancer survivors is a critical next step for optimizing cancer outcomes. It is unknown whether self-weighing and activity monitoring is a feasible strategy for breast cancer survivors to monitor weight changes and regulate their energy balance. Thus, this three-arm, pilot randomized controlled trial will evaluate two behavioral self-regulation interventions for weight gain prevention (self-regulation or self-regulation plus activity monitoring) compared to a delayed control group among 45 female African-American post-treatment breast cancer survivors. Participants will be randomly assigned to one of three groups: Self-regulation intervention with activity monitoring (n=15); Self-regulation intervention (n=15); and Delayed control (n=15).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Female, age 18 or older
- •Self-identify as African American or black
- •Diagnosed with stage I-IIIA breast cancer within the last 10 years
- •Body mass index of 20-45 kg/m²
- •Completed cancer treatment (except endocrine treatment) with full recovery of any treatment associated toxicities to ≤ Grade 1 or baseline
- •No evidence of progressive disease or second primary cancers
- •Have the ability to read, write and speak English
- •Have access to the Internet and a computer on at least a weekly basis
- •Possession and usage of an Internet e-mail address or willingness to sign up for a free email account
- •Willing to be randomized
- •Physician approval to participate
排除标准
- •History of heart attack or stroke within past 6 months
- •Untreated hypertension, hyperlipidemia, or diabetes, unless permission is provided by their health care provider
- •Treatment of diabetes with insulin, due to the concerns about hypoglycemia
- •Health problems which preclude ability to walk for physical activity (e.g., lower limb amputation)
- •Report a diagnosis of psychiatric diseases (schizophrenia, bipolar disorder, depression leading to hospitalization in the past year), drug or alcohol dependency.
- •Report a past diagnosis of or treatment for a Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition-Text Revision (DSM-IV-TR) eating disorder (anorexia nervosa or bulimia nervosa)
- •Plans for major surgery (including breast reconstruction) during the intervention time frame
- •Have lost and maintained a weight loss of > 10 pounds within the past 6 months or currently participating in another weight loss program
- •Currently using prescription weight loss medications
- •Currently pregnant, pregnant within the past 6 months, or planning to become pregnant within the next 6 months
- •Inability to attend 3 assessment visits (baseline, 3 months, and 6 months) at the University of North Carolina Weight Research Program center
结局指标
主要结局
Proportion of participants with completed assessments at 6 months
时间窗: 6 months
Proportion of participants who complete all 6-month online and in-clinic assessments.
次要结局
- Change in hemoglobin A1c(Baseline, 6 months)
- Change in waist circumference(Baseline, 6 months)
- Change in blood pressure(Baseline, 6 months)
- Weight change(Baseline, 6 months)
- Change in triglycerides(Baseline, 6 months)
- Change in dietary intake(Baseline, 6 months)
- Change in physical activity(Baseline, 6 months)
- Change in cholesterol(Baseline, 6 months)
- Proportion of participants with completed assessments at 3 months(3 months)