Psychometric Properties of the Sexual Event Diary in a Sample of Dutch Women With Female Sexual Interest/Arousal Disorder

被引:5
|
作者
van Nes, Yvonne [1 ]
Bloemers, Jos [1 ,2 ,3 ]
Kessels, Rob [1 ]
van der Heijden, Peter G. M. [4 ,5 ]
van Rooij, Kim [1 ,2 ,3 ]
Gerritsen, Jeroen [1 ,2 ,3 ]
DeRogatis, Leonard [6 ,7 ]
Tuiten, Adriaan [1 ]
机构
[1] Emot Brain BV, Louis Armstrongweg 78, NL-1311 RL Almere, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Utrecht, Netherlands
[3] Univ Utrecht, Rudolf Magnus Inst Neurosci, Utrecht, Netherlands
[4] Univ Utrecht, Dept Social Sci Methodol & Stat, Utrecht, Netherlands
[5] Univ Southampton, Southampton, Hants, England
[6] Johns Hopkins Sch Med, Psychiat, Baltimore, MD USA
[7] Maryland Ctr Sexual Hlth, Lutherville Timonium, MD USA
来源
JOURNAL OF SEXUAL MEDICINE | 2018年 / 15卷 / 05期
关键词
Sexual Event Diary; Dutch; Patient-Reported Outcome; Psychometric Properties; Satisfactory Sexual Event; Sexual Function; Female Sexual Interest/Arousal Disorder; Flypoactive Sexual Desire Disorder; DISTRESS SCALE FSDS; SUBLINGUAL TESTOSTERONE; COMBINATION TABLET; INDEX FSFI; VALIDATION; AROUSAL;
D O I
10.1016/j.jsxm.2018.03.082
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Efficacy of on-demand drugs for women with hypoactive sexual desire disorder or female sexual interest/arousal disorder (FSIAD) should be assessed using a validated instrument that assesses the discrete sexual events during which the on-demand drug is taken, because this type of assessment is more proximate to an on-demand drug's efficacy compared to instruments that assess sexual function over longer periods of time. Aim: The aim of this study was to assess the psychometric properties of the Dutch translation of the previously validated 11-item Sexual Event Diary (SED) for measuring sexual satisfaction and sexual functioning during discrete sexual events. Methods: Psychometric assessment was performed on data of 1,840 SEDs from 139 women with hypoactive sexual desire disorder/FSIAD, collected during a randomized clinical cross-over trial conducted in the Netherlands. Outcomes: Item scores of the SED at the event level, and at subject level, summarized item scores during the placebo run-in period (PRI) and active treatment period, and score changes from PRI to active treatment period. Results: Reliability and convergent validity were confirmed. All item scores showed the ability to discriminate between known groups. Larger mean score changes from PRI were observed in groups with known benefit from the medication, as compared to those with no benefit. Guyatt effect sizes ranged from 0.51 - 1.02, thereby demonstrating ability to detect change. Clinical Translation: The Dutch version of the SED is an excellent instrument for assessing female sexual functioning and sexual satisfaction during discrete sexual events and for assessing these concepts over longer periods of time. Conclusions: Data were collected in a randomized, well-controlled trial. The large number of data points gave high statistical power, and the results confirmed previous findings. Elowever, care is needed when generalizing the SED's validity to other areas of research, eg, recreational drug use and sexual risky behaviors, since the current validation study has not used such data. Consistent with the US-English version, the Dutch version of the SED is a reliable, valid, and responsive instrument, and suitable for use in evaluating effects of on-demand drugs in women with FSIAD. Copyright (C) 2018, International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:722 / 731
页数:10
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