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临床试验/NCT04597151
NCT04597151已完成不适用

Diet Education Among Colorectal Cancer Survivors in the Safety Net Setting: A Pilot Feasibility Study

University of California, San Francisco2 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2020年10月12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
13
试验地点
2
主要终点
Frequency of reasons for not participating in questionnaires

研究概览

简要总结

This pilot trial evaluates the feasibility of a group diet education program for stage I-IV colorectal cancer survivors. Providing a nutrition education program for colon and rectal cancer survivors may help them have better access to the tools necessary to make healthy food decisions that can impact their cancer outcomes.

详细描述

PRIMARY OBJECTIVE:

I. To describe the feasibility and acceptability of a group diet education intervention for colorectal cancer (CRC) survivors at Zuckerberg San Francisco General Hospital (ZSFGH).

SECONDARY OBJECTIVE:

I. To describe perceived barriers to healthy diet among CRC survivors at ZSFGH.

EXPLORATORY OBJECTIVES:

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able to speak and read English or Spanish
  • Diagnosed with stage 1- 4 colorectal cancer within 5 years prior to study enrollment and treated with curative intent
  • Receiving survivorship follow up care at Zuckerberg San Francisco General Hospital (ZSFGH)
  • Able to provide written consent

排除标准

  • Currently receiving chemotherapy, biologic therapy, radiation, or immunotherapy for colorectal cancer

结局指标

主要结局

Frequency of reasons for not participating in questionnaires

时间窗: Up to 17 weeks

Feasibility of measurement tools will be assessed by recording and reporting reasons for not taking part in questionnaires.

Percentage of participants missing questionnaires

时间窗: Up to 17 weeks

Feasibility of measurement tools will be assessed by reporting the percentage of participants whom did not complete the questionnaires

Follow-up response rates

时间窗: Up to 17 weeks

Feasibility of measurement tools will be assessed by follow up response rates (week 6 and week 17)

Percentage of consented patients who remain on the study

时间窗: Up to 17 weeks

Subject retention will be assessed by percentage of consented patients who remain on the study at week 6 and at week 17, and reasons for dropout will be documented.

Number of participants who consent or expressed interest

时间窗: Up to 17 weeks

Subject recruitment will be assessed by number of participants who consent/number of participants who initially expressed interest, and reasons for non-participation will be documented.

Categorical responses to program evaluation survey

时间窗: Up to 17 weeks

Experience (e.g. satisfaction) will be assessed by tabulated responses to program evaluation survey. Qualitative analysis of cleaned and coded transcripts from interviews using a "constant comparison" process through which data are built into conceptual categories and themes will be performed.

Number of sessions attended

时间窗: Up to 17 weeks

Adherence to diet education intervention will be assessed by number of sessions attended and reasons for absence will be documented.

次要结局

  • Frequency of responses to the baseline socio-demographics survey(Up to 17 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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