此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Improving Contraceptive Counseling in the United States (ICC)

2022年10月31日 更新者:New York University
This project develops a contraceptive counseling protocol (CCP) grounded in scientific evidence and evaluates the CCP for promoting behaviors conducive to preventing unintended pregnancy among women. The project develops and refines the CCP using focus groups and in-depth interviews with (a) key administrators in the national office of Planned Parenthood (b) key administrators in participating Title X clinics, (c) contraceptive counselors, and (d) clients of the health centers. The CCP uses scientifically grounded principles for guiding effective decision making and provider-client communication. Ten Title X clinics are randomly assigned to one of two conditions (5 clinics per condition): (1) treatment as usual (TAU) or (2) implementation of the CCP. Approximately 150 women are selected for study participation in each clinic, yielding about 1,400 participants (half control and half CCP). Immediately following their counseling session, women complete a computer-administered interview that serves as a fidelity check and permits evaluation of the effects of the CCP on variables associated with counseling satisfaction. All women are re-interviewed by phone 6 months later and 12 months later. The effect of the CCP on method-choice effectiveness, method switching, gaps in protection, and use accuracy are evaluated.

研究概览

研究类型

介入性

注册 (实际的)

1418

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

    • New York
      • New York、New York、美国、10001
        • New York University, Silver School of Social Work

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 30年 (成人)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • Must be seeking contraception from clinic on day of recruitment

Exclusion Criteria:

  • Not seeking contraception from clinic on day of recruitment

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:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention
The intervention arm receives contraceptive counseling from counselors who underwent training on the use of evidence informed birth control counseling.
Counselors underwent training on the use of 10 best practices for contraceptive counseling.
其他名称:
  • Improving contraceptive counseling in the United States
无干预:No intervention
The no intervention arm receives contraceptive counseling from counselors who underwent no additional training beyond what they normally receive.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Patient satisfaction with counselors as assessed by 5 point Likert rating scales using questionnaire designed for this study at immediate posttest.
大体时间:immediately after counseling session
immediately after counseling session
Patient satisfaction with counseling session as assessed by 5 point Likert rating scales using a questionnaire designed for this study at immediate posttest.
大体时间:immediately after counseling session
immediately after counseling session
Patient satisfaction with clinic experience overall as assessed by 5 point Likert rating scales using a questionnaire designed for this study at immediate posttest.
大体时间:immediately after counseling session
immediately after counseling session
Patient satisfaction with clinic experience overall as assessed by 5 point Likert rating scales using a questionnaire designed for this study at 6 months.
大体时间:6 months from initial clinic visit
6 months from initial clinic visit
Patient satisfaction with clinic experience overall as assessed by 5 point Likert rating scales using a questionnaire designed for this study at 12 months.
大体时间:one year from initial clinic visit
one year from initial clinic visit

次要结果测量

结果测量
大体时间
Type of contraceptive method currently using (including none and dual use) as assessed by a questionnaire designed for this study (e.g., what method of birth control are you currently using).
大体时间:six months to one year from initial clinic visit
six months to one year from initial clinic visit

其他结果措施

结果测量
大体时间
Method switching for pill users as assessed by a questionnaire designed for this study asking current method used at posttest to determine if it is no longer the pill using questions designed for this study
大体时间:six months to one year from initial clinic visit
six months to one year from initial clinic visit
Gaps in pregnancy protection (number of weeks not using any birth control during contraceptive method switches as assessed by a questionnaire designed for this study using retrospective recall
大体时间:six months to one year from initial clinic visit
six months to one year from initial clinic visit
Counselor behavior (topics covered during counseling) as assessed by a questionnaire designed for this study asking if counselor did or did not address key topics about method use
大体时间:six months to one year from initial clinic visit
six months to one year from initial clinic visit
Pill users retrospective report of the number of missed pills using a questionnaire designed for this study
大体时间:six months to one year from initial clinic visit
six months to one year from initial clinic visit

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:James J Jaccard, PhD、New York 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

2012年10月1日

初级完成 (实际的)

2014年10月1日

研究完成 (实际的)

2015年10月1日

研究注册日期

首次提交

2016年6月2日

首先提交符合 QC 标准的

2016年6月11日

首次发布 (估计)

2016年6月15日

研究记录更新

最后更新发布 (实际的)

2022年11月2日

上次提交的符合 QC 标准的更新

2022年10月31日

最后验证

2016年6月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • FPRPA006057
  • 12-9103 (其他标识符:NYU Committee on Activities Involving Human Subjects)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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.

订阅