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临床试验/NCT05796180
NCT05796180已完成不适用

The Effect of Sexual Health Counseling Based on the BETTER Model on Postpartum Sexual Life Quality: A Randomized Controlled Study

Lokman Hekim University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年11月18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
发起方
入组人数
60
试验地点
1
主要终点
VAS satisfaction scale

研究概览

简要总结

In this study, the investigators wanted to examine the effect of sexual health counseling to women in the postpartum period on the quality of life of the participants.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Primiparous,
  • Weeks of gestation 37 weeks and over,
  • Who had a singleton pregnancy,
  • Having a sexual partner/partner,
  • Having started sexual intercourse before starting training,
  • Without a diagnosed chronic disease (DM, HT, Heart disease, etc.),
  • Labour week 37 weeks and over
  • 18 years or older,
  • Able to speak and understand Turkish,

排除标准

  • Edinburgh Postpartum Depression Scale score of 12 and above,
  • To have received training on sexual health and family planning in a hospital or other health institution other than discharge training,

研究组 & 干预措施

Behavioral: sexual health counseling based on the BETTER model

Experimental

Sexual health counseling based on the BETTER model

The content of the research will be discussed by face-to-face interviews with women who gave birth vaginally and applied to the hospital for birth control 8-10 weeks after delivery. Pre-evaluation forms will be applied to women who have agreed to participate in the study to evaluate the inclusion criteria. Women who meet the inclusion criteria will be divided into experimental-control groups using the block randomization method.

An appointment will be made for interviews with the women in the experimental group. It is planned that these meetings will be held in the form of online video calls and will last an average of 45 minutes. The final tests will be held 8 weeks after the online meetings are over.

干预措施: Behavioral: sexual health counseling based on the BETTER model (Behavioral)

Control group: Routine postpartum care

No Intervention

Routine postpartum care

Women who gave birth vaginally and applied to the hospital for postpartum controls 8-10 weeks after delivery will be interviewed face-to-face with the women and the content of the research will be mentioned. Pre-evaluation forms will be applied to the women who accepted to participate in the study to evaluate the inclusion criteria. Women who meet the inclusion criteria will be divided into experimental-control groups using the block randomization method. Women in the control group will receive routine postpartum care administered in the hospital. Women in the control group will receive routine postpartum care administered in the hospital. Post-tests will be administered 8 weeks after the first interview.

结局指标

主要结局

VAS satisfaction scale

时间窗: 8 week

Women's satisfaction with sexual life will be evaluated with the visual analog scale (VAS). It shows that women who score high on the scale, which is scored between 0 (very dissatisfied) and 10 (very satisfied), also have high sexual satisfaction.

Postpartum Sexual Life Quality Scale

时间窗: 8 week

The scale is still under development.

Arizona Sexual Experiences Scale

时间窗: 8 week

The Arizona Sexual Experiences Scale (ASEX) is a 6-point Likert-type self-report scale and consists of 5 questions. This form reveals the capacity to reach orgasm, the feeling of satisfaction, vaginal wetness, arousal and sexual drive. Each question is scored from 1 to 6. The total score ranges from 5 to 30. Low scores indicate that the sexual response is satisfactory, strong and easy, while high scores indicate the presence of sexual dysfunction. The total scale score is formed by the sum of the scores of the scale items in the scale. The cut-off point of the scale was determined as 11. A score of 5 or more for each item indicates that there is a sexual dysfunction related to that item.

次要结局

未报告次要终点

研究者

发起方
Lokman Hekim University
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Nurgül ŞİMAL YAVUZ

Lecturer

Lokman Hekim University

研究点 (1)

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