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临床试验/NCT07042646
NCT07042646已完成不适用

The Effect of Sexual and Reproductive Health Training on Sexual Function and Quality of Sexual Life in Women With Physical Disabilities: A Pilot RCT Study From a Turkiye Perspective

Amasya University1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2024年9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
已完成
入组人数
26
试验地点
1
主要终点
Quality of Sexual Life

研究概览

简要总结

This pilot randomized controlled trial will be carried out with women with physical disabilities registered at a disability center. A total of 49 participants will be randomly assigned to either the intervention group or the control group. Following a three-week follow-up period, the study will be completed, with a total of 26 participants: 16 in the intervention group and 10 in the control group . SRH training will be provided to the intervention group once a week, for a total of three sessions. At the beginning and end of the study, both groups will be administered a survey including demographic information, the Sexual Quality of Life Questionnaire-Female (SQLQ-F), and the Female Sexual Function Index (FSFI).

详细描述

Background: Ensuring that women with disabilities, who are among disadvantaged groups, maintain and improve their sexual and reproductive health (SRH) on equal terms with other women is of great importance. The purpose of this study is to examine the impact of SRH training provided to women with physical disabilities on their sexual function and quality of sexual life, as well as to assess the feasibility and acceptability of the educational intervention.

Method: This pilot randomized controlled trial will be carried out with women with physical disabilities registered at a disability center. A total of 49 participants will be randomly assigned to either the intervention group or the control group. Following a three-week follow-up period, the study will be completed, with a total of 26 participants: 16 in the intervention group and 10 in the control group . SRH training will be provided to the intervention group once a week, for a total of three sessions. At the beginning and end of the study, both groups will be administered a survey including demographic information, the Sexual Quality of Life Questionnaire-Female (SQLQ-F), and the Female Sexual Function Index (FSFI).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Those who were female between the ages of 18-65, physically disabled, married, did not have a mental health problem, did not have a communication barrier, and volunteered were included in this study.

排除标准

  • •being a man
  • •having a disability other than physical disability

研究组 & 干预措施

Intervention group

Experimental

Sexual and Reproductive Health Training program received the intervention group.

干预措施: Sexual and Reproductive Health Training program (Behavioral)

Control group

No Intervention

no intervention was the control group.

结局指标

主要结局

Quality of Sexual Life

时间窗: 1 months

The scale has 6 sub-dimensions: desire, arousal, lubrication, orgasm, satisfaction, and pain (Rosen et al., 2000). Each item is scored from 0 to 5. The highest score that can be obtained from the scale is 95.0, and the lowest score is 4.0.

次要结局

  • Sexual Function(1 months)

研究者

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

Gozde Yıldız Daş Geçim

Assist. Prof.

Amasya University

研究点 (1)

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