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临床试验/NCT05839210
NCT05839210招募中不适用

Lifestyle Intervention of Food and Exercise for Lymphoma Survivors (LIFE - L)

University of Miami1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2023年4月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
140
试验地点
1
主要终点
Percentage of Participants Completing Intervention Sessions

研究概览

简要总结

The purpose of this study is to investigate if a mediterranean diet and exercise program for Lymphoma patients during chemotherapy can improve treatment completion and reduce treatment-related side effects.

研究设计

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

入排标准

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

入选标准

  • 18 years of age or older
  • Any sex/gender
  • Able to provide consent
  • Able to read or understand English or Spanish
  • Diagnosis of untreated Non-Hodgkin or Hodgkin lymphoma, requiring at least 6 cycles of chemotherapy, being treated with one of the following therapies at discretion of PIs:
  • R-CHOP or R-CHOP-like regimen
  • BV-AVD or ABVD or checkpoint inhibitor+AVD
  • ECOG Performance Status grade of <2
  • a. PI approval needed if ECOG = 2
  • Approval from treating oncologist, confirmed via email or in writing
  • Delivery of chemotherapy treatments at one of the following institutions:
  • Sylvester Comprehensive Cancer Center (including satellite/network sites)
  • University of Miami Hospital/UHealth Tower
  • Internet access on a smart phone, tablet, or computer
  • Willing to be randomized to a Mediterranean diet/home-based physical activity intervention or waitlist-control group.

排除标准

  • Individuals younger than 18 years of age
  • Unable to provide consent
  • Unable to read or understand English or Spanish
  • Any contraindication for diet change or exercising as determined by physician
  • Currently following a vegan or ketogenic diet, or consuming more than 5 servings of fruit and vegetables per day for the prior month
  • Engaging in >150 minutes of moderate to vigorous physical activity on average per week for the prior month
  • History of dementia or major psychiatric disease
  • History of recent (≤1 yr) stroke, myocardial infarction or congestive heart failure

研究组 & 干预措施

LIFE-L Group

Experimental

Participants already undergoing chemotherapy treatment as per standard of care for 6 cycles will meet weekly via phone for 30-45 minutes with a health coach that will provide education on a Mediterranean diet and an exercise program.

干预措施: LIFE-L Mediterranean Diet (Behavioral)

LIFE-L Group

Experimental

Participants already undergoing chemotherapy treatment as per standard of care for 6 cycles will meet weekly via phone for 30-45 minutes with a health coach that will provide education on a Mediterranean diet and an exercise program.

干预措施: LIFE-L Home-Based Exercise Program (Behavioral)

LIFE-L Group

Experimental

Participants already undergoing chemotherapy treatment as per standard of care for 6 cycles will meet weekly via phone for 30-45 minutes with a health coach that will provide education on a Mediterranean diet and an exercise program.

干预措施: Supportive Materials (Behavioral)

Control Group

Other

Participants in this group already undergoing 6 cycles of chemotherapy will receive study materials and two 30-45 minutes health coaching sessions four weeks post- intervention.

干预措施: Supportive Materials (Behavioral)

结局指标

主要结局

Percentage of Participants Completing Intervention Sessions

时间窗: Up to 26 weeks (Post-Intervention)

Percentage of intervention session completion at the end of treatment will be assessed, using a threshold of greater than or equal to (\>=) 80-percent.

Change in percentage of participant satisfaction

时间窗: 4 weeks (post-intervention), up to 30 weeks

The change in percentage of participant satisfaction rate at the end of study participation will be assessed, using a threshold of greater than or equal to (\>=) 80-percent. Participant satisfaction will be assessed via exit interviews.

Percentage of Survivors who participate

时间窗: Up to 12 months

Percentage of survivors who agree to participate out of the total number of participants recruited will be assessed using a threshold of greater than or equal to (\>=) 50-percent.

次要结局

  • Average Relative Dose Intensity (RDI)(Up to 30 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tracy E Crane, PhD, RDN

Associate Professor

University of Miami

研究点 (1)

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