跳至主要内容
临床试验/NCT00499759
NCT00499759已完成不适用

In-Hospital Individualized Prescriptive Exercise Intervention for Acute Leukemia Patients Undergoing Chemotherapy

UNC Lineberger Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2006年2月1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
10
试验地点
2
主要终点
Effects of an individualized prescriptive exercise intervention

研究概览

简要总结

RATIONALE: An individualized exercise program may be effective in lessening fatigue and depression and improving quality of life in patients undergoing chemotherapy for leukemia.

PURPOSE: This clinical trial is studying how well individualized exercise programs work in patients receiving chemotherapy for newly diagnosed acute or relapsed myeloid leukemia or lymphoblastic leukemia.

详细描述

OBJECTIVES:

Primary

  • Determine the effects, in terms of fitness and blood parameters, fatigue levels, and quality of life, of an individualized prescriptive exercise intervention in patients with newly diagnosed acute or relapsed myeloid or lymphoblastic leukemia undergoing chemotherapy.

Secondary

  • Determine the feasibility of developing an exercise program for these patients.
  • Assess the changes in cardiovascular endurance, muscular strength, selected blood parameters, and response of inflammatory proteins to exercise in these patients.
  • Evaluate fatigue, depression, and quality of life of these patients.

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
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • DISEASE CHARACTERISTICS:
  • Newly diagnosed acute or relapsed myeloid or lymphoblastic leukemia
  • Currently receiving re-induction therapy or designated for chemotherapy treatment
  • Expected hospital stay of 3-4 weeks or longer
  • Participation in the study must be approved by the physician directly responsible for the patient's care while at University of North Carolina Hospitals
  • PATIENT CHARACTERISTICS:
  • No condition that would compromise the patient's ability to participate in the exercise rehabilitation program, including any of the following:
  • Immune deficiency
  • Acute or chronic bone, joint, or muscular abnormalities
  • Acute or chronic respiratory disease
  • Cardiovascular disease
  • PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics

排除标准

  • 未提供

结局指标

主要结局

Effects of an individualized prescriptive exercise intervention

时间窗: 6 weeks

All patients will participate in an individualized prescriptive exercise intervention 3 to 4 times per week (depending on the physical status of each patient during each week) for a period of 6 weeks. The exercise intervention will begin on week 1 of the study, the day after the first battery of initial assessments is concluded. Each exercise session will be divided into two bouts. One bout will be administered in the morning and the second one late in the afternoon

次要结局

  • Number of subjects experiencing fatigue, depression, and quality of life issues(6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验