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Arab American Women's Health Study

2018年10月1日 更新者:Mark A. Lumley、Wayne State University
This study evaluates how Arab American women's cultural values and sexual health are related to their physical and emotional health. The study will also examine whether engaging in a sexual health interview affects women's physical and emotional health.

研究概览

地位

完全的

详细说明

Sexuality is an important aspect of health, in part because emotional conflicts over sexuality as well as unwanted sexual experiences can impact physical and psychological health; yet no studies have examined sexual health among Arab American women in the U.S. These women face the task of negotiating their heritage culture and the American culture in which they reside. This may result in bicultural identity conflict for some women as they try to negotiate these two identities, which may have implications for sexuality and sexual health due to the two cultures' disparate views on sexuality. Confidential discussion of these sensitive topics with a knowledgeable interviewer may yield beneficial effects.

The overall goal of the current study is to fill the gap in the literature on Arab American sexual health by examining how sexual health is related to physical and psychological health. This will be accomplished using both: a) correlational findings about sexual, physical, and psychological health from information gathered through self-report questionnaires and a 60-minute women's health interview; and b) an experimental test of the effects of the women's health interview on physical and psychological health. A sample of young adult Arab American women will be assessed at baseline via questionnaires for various constructs (sexual attitudes, cultural and religious identity, and physical and mental health), and then randomized to either an immediate or delayed health interview, with a 5-week follow-up reassessment.

It is hypothesized that lower sexual well-being, negative sexual self-schemas, and unwanted sexual experiences will correlate with more somatic and psychological health symptoms and lower satisfaction with life. It is also hypothesized that participants who have the immediate interview will report greater reduction in somatic and psychological symptoms and a greater willingness to discuss sexual health with medical providers compared to participants who are not interviewed (i.e., have a delayed interview after follow-up assessment).

研究类型

介入性

注册 (实际的)

134

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Michigan
      • Detroit、Michigan、美国、48201
        • Wayne State University

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 35年 (成人)

接受健康志愿者

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Arab American or Chaldean
  • Female
  • Age 18-35

Exclusion Criteria:

  • Non-English speaking

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Immediate Interview
A 60-minute interview about women's health conducted immediately after baseline questionnaires.
A women's health interview that obtains information about physical, mental, and sexual health, particularly relatively private sexual health-related attitudes and experiences, as well as conflicts and stress related to sexuality.
其他名称:
  • Women's Health Interview
无干预:Delayed Interview
The interview is conducted after the follow-up questionnaires are completed, rather than after baseline.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Patient Health Questionnaire
大体时间:Change from baseline to 5-week follow-up
Physical symptoms
Change from baseline to 5-week follow-up

次要结果测量

结果测量
措施说明
大体时间
Brief Symptom Inventory
大体时间:Change from baseline to 5-week follow-up
Psychological symptoms
Change from baseline to 5-week follow-up
Satisfaction with Life Scale
大体时间:Change from baseline to 5-week follow-up
Satisfaction with life
Change from baseline to 5-week follow-up
Sexual Self-Schema Scale
大体时间:Change from baseline to 5-week follow-up
Sexual self-schemas
Change from baseline to 5-week follow-up
Sexual Self Disclosure Scale (Catania)
大体时间:Change from baseline to 5-week follow-up
Self-reported ease or difficulty with disclosing information about sexuality
Change from baseline to 5-week follow-up
Sexual Self Disclosure Scale (Herold & Way)
大体时间:Change from baseline to 5-week follow-up
Degree of past sexual disclosure
Change from baseline to 5-week follow-up
Female Sexual Function Index
大体时间:Change from baseline to 5-week follow-up
Female sexual function
Change from baseline to 5-week follow-up
Sexual Satisfaction Scale for Women
大体时间:Change from baseline to 5-week follow-up
Sexual satisfaction
Change from baseline to 5-week follow-up

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Mark Lumley, PhD、Wayne State University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2017年9月28日

初级完成 (实际的)

2018年5月24日

研究完成 (实际的)

2018年5月24日

研究注册日期

首次提交

2017年10月2日

首先提交符合 QC 标准的

2017年10月2日

首次发布 (实际的)

2017年10月6日

研究记录更新

最后更新发布 (实际的)

2018年10月2日

上次提交的符合 QC 标准的更新

2018年10月1日

最后验证

2018年10月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • 064917B3E

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

Immediate interview的临床试验

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