Department of Health Sciences Research, Division of Health Care Policy & Research, Mayo Clinic, Rochester, MN 55905, USA.
Sex Transm Dis. 2012 Jan;39(1):28-31. doi: 10.1097/OLQ.0b013e318231575f.
Developing effective and safe microbicides requires study procedures (e.g., technology used, abstinence requirements, and product use) that are acceptable to participants.
Thirty women completed 4 study visits including pelvic examination, colposcopy, optical coherence tomography (OCT), and semistructured, qualitative interviews. Additional requirements included abstinence (for approximately 16 days) and twice daily vaginal product use (for 5.5 days). Interviews were audio-recorded, transcribed, and analyzed using framework analysis. Themes addressing OCT experiences, acceptability of abstinence, and vaginal product use were examined.
OCT was viewed favorably as an imaging technology. Some women reported feeling the fiber-optic probe "poking" them and more than one-third spontaneously reported feeling pressure or pinching upon rotation of the speculum in connection with the OCT evaluation. Compliance with vaginal gel use was high, but for many women assigned to use a product containing nonoxynol-9 (vs. placebo), the postproduct use examination was more uncomfortable, relative to the initial examination or 1 week following product discontinuation. Nearly all women experienced product leakage; acceptability of leakage varied. Two women were not abstinent and several more found abstinence challenging. Some women involved their partner in decision making regarding trial enrollment. Strategies to remain abstinent included participating when the partner was away, avoiding early intimacy, and engaging in alternative sexual activities.
Qualitative interviews in early-phase studies provide insights and capture information that would be missed by behavioral inference alone. Understanding participant's experiences is important in order to provide anticipatory guidance and plan future microbicide studies that facilitate adherence with trial requirements.
开发有效且安全的杀微生物剂需要研究程序(例如,使用的技术、禁欲要求和产品使用),这些程序必须被参与者接受。
30 名女性完成了 4 次研究访问,包括盆腔检查、阴道镜检查、光学相干断层扫描(OCT)和半结构化定性访谈。其他要求包括禁欲(大约 16 天)和每天两次阴道产品使用(5.5 天)。访谈进行了录音、转录,并使用框架分析进行了分析。检查了关于 OCT 体验、禁欲可接受性和阴道产品使用的主题。
OCT 作为一种成像技术受到了好评。一些女性报告说感觉光纤探头“戳”了她们,超过三分之一的女性在阴道镜检查时自发报告感到压力或挤压,这与 OCT 评估有关。阴道凝胶使用的依从性很高,但对于许多使用含有壬苯醇醚-9(与安慰剂相比)的产品的女性来说,相对于初始检查或产品停用 1 周后,使用后检查更不舒服。几乎所有女性都经历了产品泄漏;对泄漏的接受程度各不相同。有两名女性没有禁欲,还有更多女性发现禁欲有困难。一些女性让伴侣参与试验入组的决策。保持禁欲的策略包括在伴侣不在时参与、避免早期亲密关系以及从事替代性行为。
早期研究中的定性访谈提供了仅凭行为推断会错过的见解和信息。了解参与者的体验对于提供预期指导和计划未来促进试验要求遵守的杀微生物剂研究非常重要。