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临床试验/NCT02135211
NCT02135211已完成不适用

Feasibility and Acceptability of a Lifestyle Intervention for Patients Receiving Surgical Treatment for Lung Surgery

Dana-Farber Cancer Institute4 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2012年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
4
主要终点
Feasibility and acceptability

研究概览

简要总结

The objective of this proposal is to test the feasibility and acceptability of a lifestyle risk reduction intervention for patients with lung cancer receiving surgical treatment. This study will provide the preliminary data needed to conduct a larger randomized controlled trial that tests an innovative, multidisciplinary intervention that has the potential to transform the standard of care for patients receiving surgical treatment for lung cancer.

研究设计

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

入排标准

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

入选标准

  • > 21 years of age
  • English speaking
  • MD approval to participate in study
  • Meets one of the inclusions below:
  • a histological diagnosis of NSCLC undergoing potentially curative treatment
  • OR those undergoing surgical procedures for lung cancer (includes patients undergoing diagnostic testing or those presenting with lung nodules
  • 3.OR patients who have had a surgical procedure for lung cancer within the last six months.
  • May invite a buddy to join study with them defined as a friend, partner, adult child or sibling
  • Buddy Inclusion Criteria:
  • ≥ 21 years of age,
  • English speaking, who is invited by the subject to join as a support person (e.g., friend, partner, adult child or sibling)

排除标准

  • 未提供

研究组 & 干预措施

Lifestyle counseling

Experimental

This is a single arm, quasi-experimental, pre- and post- test study design to test the feasibility and acceptability of a multiple risk factor, lifestyle intervention in patients receiving surgical treatment for lung cancer or those suspected of having lung cancer.

干预措施: Lifestyle counseling (Behavioral)

结局指标

主要结局

Feasibility and acceptability

时间窗: at end of study (4 months post intervention)

The primary outcome measures to establish feasibility and acceptability of the intervention for this study are enrollment rates.

次要结局

  • Interest for this study(baseline, 1 month, & 4 month)

研究者

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

Mary E. Cooley, Phd

Nurse Scientist, PhD, CRNP, FAAN

Dana-Farber Cancer Institute

研究点 (4)

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