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临床试验/NCT05842031
NCT05842031暂停不适用

Assessment of Patient Experience and Needs for Patients Undergoing Invasive Inguinal Lymph Node Procedures for Penile Cancer

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年4月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
暂停
入组人数
20
试验地点
1
主要终点
Decision Regret Scale (DRS) questionnaires

研究概览

简要总结

To learn more about the patient experience undergoing inguinal (in the groin) lymph node procedures for penile cancer during and after surgery.

详细描述

Objectives

Primary Objective:

To understand the lived experience of patients undergoing invasive inguinal lymph node procedures.

Secondary Objective:

To determine factors that influence decisions and improve experience for patients who need invasive inguinal lymph node procedures.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • •-Patients diagnosed with penile cancer who have undergone invasive inguinal node procedures (ILND and/or DSNB) and are at least 6 months post-procedure

排除标准

  • •Patient's ≤18 years of age
  • •Patients who have not undergone invasive surgical procedures involving the inguinal lymph nodes
  • •Non-English-speaking patients For interviews: people who are physically and/or cognitively incapable of participating in a 60minute telephone interview as determined by a clinical provider or the patient.

研究组 & 干预措施

Semi-structured interviews

Participants with penile cancer who have undergone invasive inguinal lymph node procedure will be recruited to participate in study via telephone recruitment.

干预措施: Quality of Life Questionnaires (Behavioral)

Semi-structured interviews

Participants with penile cancer who have undergone invasive inguinal lymph node procedure will be recruited to participate in study via telephone recruitment.

干预措施: Patient Educational Needs (Behavioral)

Semi-structured interviews

Participants with penile cancer who have undergone invasive inguinal lymph node procedure will be recruited to participate in study via telephone recruitment.

干预措施: Symptom Management (Behavioral)

结局指标

主要结局

Decision Regret Scale (DRS) questionnaires

时间窗: through study completion; an average of 1 year

Score Scale ranges (1-5) 1. Strongly Agree 2. Agree 3. Agree nor Disagree 4. Disagree 5. Strongly Disagree

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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