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临床试验/NCT02000986
NCT02000986撤回不适用

Effect of Non-Pharmacologic Interventions on Risk Factors of Cardiovascular Disease in Survivors of Childhood Leukemia, Lymphoma and Brain Tumor

Virginia Commonwealth University0 个研究点开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Feasibility determined by average attendance and retention

研究概览

简要总结

This clinical trial studies dietary and exercise interventions in preventing cardiovascular disease in younger survivors of childhood cancer. Eating a healthy diet and exercising regularly may reduce the risk of cardiovascular disease in younger survivors of childhood cancer.

详细描述

Participants receive personalized exercise plan and prescription tailored to individual needs and current level of activity and fitness, and they also receive 2 one-hour individual exercise training sessions consisting of 20-30 minutes cardiovascular activity and strength training. Participants receive nutritional education consisting of energy balance, appropriate portion sizes, calorie count, and basic nutrition skills such as label reading every 2 weeks for 12 weeks.

After completion of study treatment, patients are followed for up to 6 months.

研究设计

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

入排标准

年龄范围
11 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of pediatric cancer
  • Patients 3 months to 1 year after completion of therapy

排除标准

  • Patients who are already on antihypertensive or insulin or cholesterol lowering medication
  • Patients who have not been evaluated for exercise tolerance and cleared by their physician for participation
  • Inability to understand program instructions due to language barrier or mental disability
  • Unable to participate in the outlined exercise program due to a physical disability

结局指标

主要结局

Feasibility determined by average attendance and retention

时间窗: At 3 months

Acceptability will be determined by responses on feedback measures and qualitative analysis of exit interviews.

次要结局

  • Feasibility determined by average attendance and retention from the blood pressure at enrollment(At 6 months)
  • Acceptability level at time of enrollment(At 6 months)

研究者

申办方类型
Other
责任方
Sponsor

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