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临床试验/NCT04189263
NCT04189263终止2 期

IIT2018-21-Amersi-BREADS BREADS: Breast Adjuvant Diet Study

Farin Amersi1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2020年2月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
6
试验地点
1
主要终点
Mean change in weight

研究概览

简要总结

This is a randomized controlled trial of a 6-month extreme carbohydrate restricted diet (20 grams total carbs/day) via phone counseling with dietitian plus aromatase inhibitor therapy vs. 6-month control with aromatase inhibitor therapy alone. Visits will occur at screening, 3 months, and 6 months. Anthropomorphic measurements (such as heart rate, weight, and body measurement) and questionnaires will be taken at all three visits. After screening, patients will be randomized to receive the carbohydrate restricted diet coaching immediately (Arm A) or to a control group (Arm B). Patients randomized to Arm A will receive weekly calls for the first 3 months of the intervention, then biweekly calls for the last 3 months of the intervention from the study dietitian. Total duration of the study is expected to be 3 years, though each patient's participation will be approximately 6 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • Histologically confirmed breast cancer
  • Planning to start adjuvant hormonal therapy using an aromatase inhibitor or has started adjuvant hormonal therapy using an aromatase inhibitor
  • Able to read, write, and understand English
  • BMI ≥ 24 kg/m2
  • Age ≥ 18 years
  • ER and/or PR positive (defined as having ≥ 1% staining for ER and/or PR on IHC)
  • Post-menopausal
  • The absence of menstrual cycles in women who have not undergone hysterectomy for at least 12 months preceding cancer diagnosis OR
  • History of a bilateral oophorectomy OR
  • History of a hysterectomy and age >55 OR
  • No menses for <1 year with FSh and estradiol levels in postmenopausal range according to institutional standards
  • ECOG Performance Status 0 or 1
  • Written informed consent obtained from subject and ability for subject to comply with requirements of the study

排除标准

  • Use of hormonal therapy other than aromatase inhibitors
  • History of other malignancy within the past 5 years, except for malignancies with a > 95% likelihood of cure (e.g. thyroid cancer, non-melanoma skin cancer)
  • Already consuming a severe carbohydrate restricted (<20 g carbohydrates per day) diet or vegetarian diet
  • Currently on or plans to start chemotherapy (HER2/neu targeted therapy okay)
  • Medical comorbidities that in the opinion of the investigator limits the patient's ability to complete the study
  • Symptomatic metastases (Metastases allowed if asymptomatic)
  • Current use of appetite suppressant medications
  • Current use of any weight loss medications including herbal weight loss supplements or if patients are enrolled in a diet/weight loss program

研究组 & 干预措施

Dietary intervention

Experimental

Carbohydrate restricted dietary intervention (<20 g carbohydrates/day) + standard of care aromatase inhibitors

干预措施: Carbohydrate restricted dietary intervention (Other)

Dietary intervention

Experimental

Carbohydrate restricted dietary intervention (<20 g carbohydrates/day) + standard of care aromatase inhibitors

干预措施: standard of care aromatase inhibitors (Drug)

No dietary intervention

Active Comparator

Standard of care aromatase inhibitors

干预措施: standard of care aromatase inhibitors (Drug)

结局指标

主要结局

Mean change in weight

时间窗: 6 months

Difference in change in weight between pre- and post- intervention between carbohydrate restricted and control group

次要结局

  • Changes in insulin(6 months)
  • Changes in HbA1c(6 months)
  • Changes in triglycerides(6 months)
  • Changes in cholesterol(6 months)
  • Changes in serum estradiol(6 months)
  • Changes in fasting glucose(6 months)
  • Changes in LDL(6 months)
  • Changes in HDL(6 months)

研究者

发起方
Farin Amersi
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Farin Amersi

Associate Professor, Surgery

Cedars-Sinai Medical Center

研究点 (1)

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