Abstract

The female orgasm represents one of the most complex functions in the field of human sexuality.The conjunction of the anatomical, physiological, psycho-relational and socio-cultural components contributes to make the female orgasm still partly unclear. The female orgasmic experience, its correlates and the relation with sexual desire, arousal and lubrication as predictors are highly debated in scientific community. In this context, little is known about the impact of female sexual dysfunction (SD) on sexual pleasure expressed by subjective orgasmic intensity, and there are no suitable psychometric tools suited to investigate this dimension. Thus, we validate, in female subjects, a Visual Analogue Scale (VAS) that we named Orgasmometer-F, to verify if SD is accompanied by a lower perceived orgasmic intensity. A total of 526 women, recruited through a web-based platform and from sexological outpatient clinic, were enrolled in the study. They were divided into, on the basis of the Female Sexual Function Index (FSFI) score in two groups: 1) 112women suffering from SD, (SD Group); and 2) 414 sexually healthy women (Control Group). The participants were requested to fill out the Orgasmometer-F, recording orgasmic intensity on a Likert scale from 0 (absence of orgasmic intensity) to 10 (maximum orgasmic intensity experienced). Women with SD experienced significantly lower orgasmic intensity than controls, as measured by the Orgasmometer-F (p < 0.0001). Interestingly, masturbatory frequency was positively correlated with orgasmic intensity, as were the lubrication, orgasm and sexual satisfaction domains of the FSFI. The Orgasmometer-F was well understood, had a good test-retest reliability (ICC = 0.93) and a high AUC in differentiating between women with and without sexual dysfunction (AUC = 0.9; p < 0.0001). The ROC curve analysis showed that a cut-off <5 had 86.5% sensitivity (95% CI 82,8–89,6), 80.4% specificity (95% CI 71.8–87.3), 75.4% positive predictive value (PPV) and 89.5% negative predictive value (NPV). In conclusion, the Orgasmometer-F, a new psychometrically sound tool for measuring orgasmic intensity in female population, demonstrated that SD impair orgasmic intensity.

Highlights

  • Female orgasm is a neuromuscular phenomenon triggered by sexual stimuli, accompanied by anatomical and physiological responses including vasocongestion of the erectile tissues, lubrication, and pelvic contractions that induce intense pleasurable sensations [1,2,3,4,5]

  • There is a larger area involved in sexual stimulation, called the clitourethrovaginal (CUV) complex [15,16,17], a variable, multifaceted morpho-functional area that, when properly stimulated during penetration, could induce orgasmic response

  • Intraclass correlation coefficient (ICC) analysis was performed on Orgasmometer-F repeated measures, collected on day 0 and 14 (n = 35)

Read more

Summary

Introduction

Female orgasm is a neuromuscular phenomenon triggered by sexual (somatic and mental) stimuli, accompanied by anatomical and physiological responses including vasocongestion of the erectile tissues, lubrication, and pelvic contractions that induce intense pleasurable sensations [1,2,3,4,5] This female orgasm is not yet fully understood and defined, because of the great variability in factors including localization [6,7,8], stimulation techniques [9,10], self-image [11,12,13] and quality of romantic relationship [10,14]. There is a larger area involved in sexual stimulation, called the clitourethrovaginal (CUV) complex [15,16,17], a variable, multifaceted morpho-functional area that, when properly stimulated during penetration, could induce orgasmic response

Objectives
Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.