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临床试验/NCT05335967
NCT05335967已完成不适用

Development and Effectiveness Evaluation of a Self-management Program for Prostate Cancer Survivors

National Taipei University of Nursing and Health Sciences2 个研究点 分布在 1 个国家目标入组 85 人开始时间: 2022年5月20日最近更新:
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
85
试验地点
2
主要终点
Cancer related self-efficacy

研究概览

简要总结

Objectives: This project aims to develop a self-management program for survivors with prostate cancer experiencing urinary incontinence following radical prostatectomy and determine its effectiveness.

Methods: The investigators will develop a self-management program and conduct a study on survivors with prostate cancer experiencing urinary incontinence following radical prostatectomy. And the investigators will test the effectiveness of the self-management program. After completing a pretest, participants will be randomly assigned to the experimental or control group. The self-management group will receive the self-management program for 12 weeks, whereas the information group will receive an information package on a healthy diet. Posttests will be administered 12 and 16 weeks after the pretest. The study variables will include physical symptoms and bothers, cancer-related self-efficacy, social participation, demoralization, and resilience.

详细描述

Objectives: This project aims to develop a self-management program for survivors with prostate cancer experiencing urinary incontinence following radical prostatectomy and determine its effectiveness.

Methods: The investigators will develop a self-management program and conduct a study on survivors with prostate cancer experiencing urinary incontinence following radical prostatectomy. And the investigators will test the effectiveness of the self-management program. After completing a pretest, participants will be randomly assigned to the experimental or control group. The self-management group will receive the self-management program for 12 weeks, whereas the information group will receive an information package on a healthy diet. The self-management program is included a self-management application, a self-management manual, and professional support. The information package consists of a manual on a healthy diet and a multimedia film on a healthy diet. Posttests will be administered 12 and 16 weeks after the pretest. The study variables will include physical symptoms and bothers, cancer-related self-efficacy, social participation, demoralization, and resilience. The statistical analyses will consist of independent sample t-tests, Chi-squire, and generalized estimating equation analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Prostate cancer survivors will include if they fit the following:
  • •Received radical prostatectomy and suffering from urinary incontinence for at least one week
  • •Eastern Cooperative Oncology Group 0-1 point, able to walk entirely independently
  • •Have a smartphone or a tablet with a wireless network
  • •Their intimate partner or one of the family members willing to learn together
  • •Agreed to participate in the study and completed the informed consent form

排除标准

  • •Prostate cancer survivors will be excluded if they had one or more of the following:
  • •A request, with the consideration of family members, that the medical team not tell the patient about the diagnosis or condition of the disease
  • •A history of psychiatric illness, such as dementia, depression; schizophrenia, or bipolar disorder
  • •Suffer from other types of cancer and actively undergoing treatment

研究组 & 干预措施

Self-management group

Experimental

The experimental group will receive the self-management program for 12 weeks.

干预措施: Self-management program (Behavioral)

Information group

Other

The control group will receive an information package on a healthy diet.

干预措施: Information package (Other)

结局指标

主要结局

Cancer related self-efficacy

时间窗: 16 weeks after the pretest

The Mandarin version of the Cancer Survivors' Self-Efficacy Scale (CSSES) will be used to evaluate the cancer-specific self-efficacy of participants.The total score ranges from 11 to 110; the lower the score, the worse the self-efficacy.

Cancer related self-efficacy

时间窗: Pre-test

The Mandarin version of the Cancer Survivors' Self-Efficacy Scale (CSSES) will be used to evaluate the cancer-specific self-efficacy of participants.The total score ranges from 11 to 110; the lower the score, the worse the self-efficacy.

Cancer related self-efficacy

时间窗: 12 weeks after the pretest

The Mandarin version of the Cancer Survivors' Self-Efficacy Scale (CSSES) will be used to evaluate the cancer-specific self-efficacy of participants.The total score ranges from 11 to 110; the lower the score, the worse the self-efficacy.

次要结局

  • Urinary symptoms and bothers(16 weeks after the pretest)
  • Social participation(16 weeks after the pretest)
  • Demoralization(16 weeks after the pretest)
  • Resilience(16 weeks after the pretest)
  • Urinary symptoms and bothers(Pre-test)
  • Urinary symptoms and bothers(12 weeks after the pretest)
  • Social participation(Pre-test)
  • Social participation(12 weeks after the pretest)
  • Demoralization(Pre-test)
  • Demoralization(12 weeks after the pretest)
  • Resilience(Pre-test)
  • Resilience(12 weeks after the pretest)

研究者

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

Ching-Hui Chien

RN, PhD, Professor

National Taipei University of Nursing and Health Sciences

研究点 (2)

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