跳至主要内容
临床试验/NCT01159678
NCT01159678已完成不适用

Online Psychoeducation for Sexual Dysfunction in Cancer Survivors

University of British Columbia2 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2010年10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
112
试验地点
2
主要终点
Sexual distress

研究概览

简要总结

The purpose of this study is to test an online psychoeducational intervention for men and women with sexual difficulties after surgery for colorectal (men and women) or gynecological (women only) cancer. A psychoeducational intervention is a brief, educational treatment that encourages participants to also pay attention to, and modify, their thoughts, feelings, and behaviour.

详细描述

Experiencing a diagnosis of cancer may dramatically alter the way a person feels about themselves, their body, and their significant relationships at sexual and intimate levels1. Cancer and its treatments affect the physiological, psychological, and sociological realms of a survivor's life and his/her ability to experience sexual health. Sexual health is recognized as an integral aspect of quality of life (QOL) during cancer and is increasingly receiving research and clinical attention. Sexual changes following the treatment of gynaecologic (i.e.: ovarian, endometrial, cervical) and colorectal cancers are common though often not discussed. Moreover, cancer survivors express dissatisfaction that sexual concerns, and treatment of them, are not discussed in the context of their cancer care. Oncologists frequently are faced with patients inquiring about sexual changes with cancer treatment, but are usually not equipped with accurate and comprehensive data on the precise sexual symptoms to expect or where to refer patients with sexual concerns.

The aims of the study are to assess the efficacy of a 12-module online psychoeducational intervention for sexual health (OPES) on (1) the primary endpoint of sexual distress in male and female cancer survivors with sexual problems; (2) the secondary sexuality-related endpoints of sexual desire, arousal (women) or erection (men), orgasm, and sexual pain; (3) on mood, relationship satisfaction, and quality of life; and (4) to assess gender differences in the proportion of survivors improved on sexual distress.

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
19 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • aged 19-70,
  • treatment of gynaecologic or colorectal cancer by one of the surgical oncologists of the gynaecology or colorectal teams of the BC Cancer Agency centres or satellite sites,
  • received treatment in the past 5 years
  • currently in a relationship
  • currently experiencing sexual dysfunction, and
  • able to participate (both physically and emotionally) in completion of an online psychoeducational treatment.

排除标准

  • 未提供

研究组 & 干预措施

online psychoeducation

Experimental

干预措施: online psychoeducation (Behavioral)

结局指标

主要结局

Sexual distress

时间窗: Questionnaires administered 1 week pre-treatment, 1 week post treatment and six months post treatment

measured by self report questionnaires

次要结局

  • Sexual function(Questionnaires administered 1 week pre-treatment, 1 week post- treatment and six months post treatment)

研究者

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

Lori Brotto

Associate Professor

University of British Columbia

研究点 (2)

Loading locations...

相似试验