跳至主要内容
临床试验/NCT06840847
NCT06840847已完成不适用

Sexual Coercion in Breast Cancer Patients Treated With Luteinizing Hormone-Releasing Hormone Agonists (LHRHa )

Canan Kas2 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2024年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
79
试验地点
2
主要终点
LHRHa

研究概览

简要总结

The use of luteinizing hormone-releasing hormone agonists(LHRHa) to suppress ovarian function is a common strategy for treating premenopausal, hormone receptor-positive breast cancer. However, this approach can lead to more severe and prolonged menopausal symptoms, which can further impact intimate relationships and sexual function. Sexual coercion, encompassing both overt and subtle forms of pressure, is a significant global public health concern that threatens individual well-being.

详细描述

Objective

The use of luteinizing hormone-releasing hormone agonists(LHRHa) to suppress ovarian function is a common strategy for treating premenopausal, hormone receptor-positive breast cancer. However, this approach can lead to more severe and prolonged menopausal symptoms, which can further impact intimate relationships and sexual function. Sexual coercion, encompassing both overt and subtle forms of pressure, is a significant global public health concern that threatens individual well-being.

Methods: This study is a randomized controlled study. In this study, the validated Turkish version of the Sexual Coercion in Intimate Relationship Scale was utilized to investigate whether patients receiving LHRHa therapy experienced higher rates of sexual sexual coercion compared to those taking tamoxifen. The study included 40 patients using LHRHa and 39 patients using tamoxifen. The instrument assessed partner sexual coercion across three subdomains: resource manipulation/sexual coercion, commitment manipulation, and defection threat.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Factorial
主要目的
Health Services Research
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • being over 18 years of age
  • willingness to participate in this study
  • having received treatment for breast cancer
  • having a history of breast cancer surgery
  • having an active relationship with a spouse or partner.

排除标准

  • having any neuropsychiatric disorder
  • having any mental illness
  • having a history of gynecological surgery
  • currently receiving active chemotherapy or less than 3 months since completing chemotherapy
  • receiving treatment for metastatic disease
  • The use of selective serotonin reuptake inhibitors

结局指标

主要结局

LHRHa

时间窗: for 10 months

It was examined whether patients receiving LHRHa treatment were exposed to sexual pressure.

Tamoxifen

时间窗: for 10 months

It was examined whether patients receiving tamoxifen treatment were exposed to sexual pressure.

次要结局

未报告次要终点

研究者

发起方
Canan Kas
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Canan Kas

PhD, MSc, RN, Assistant Professor

Kastamonu University

研究点 (2)

Loading locations...

相似试验