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临床试验/NCT02752282
NCT02752282Unknown不适用

Anticipatory Counseling on LNG-IUS Continuation, Utilization and Satisfaction

University of Washington6 个研究点 分布在 1 个国家目标入组 178 人开始时间: 2016年3月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
178
试验地点
6
主要终点
Change in LNG-IUS knowledge, satisfaction and continuation from baseline

研究概览

简要总结

This study is a counseling intervention for new LNG-IUS users. The study explores the use of video technology to deliver anticipatory counseling on LNG-IUS side-effects, adjustment periods and bleeding changes to women newly using the LNG-IUS for contraceptive purposes. The primary aim is to understand if anticipatory counseling delivered via video can increase LNG-IUS satisfaction and continuation of the device in the first 6 months of use.

详细描述

Enhanced anticipatory counseling detailing side effects when initiating progestin-only injectable contraception improved its continued use among women.While continuation rates at one year among levonorgestrel intrauterine system (LNG-IUS) users are considerably higher than those for progestin-only injectable users in the United States (80% versus 56%), enhanced anticipatory counseling could have an impact on the 20% of LNG IUS users who choose to discontinue the method within one year of use. For this reason, the investigators propose a study that would develop and pilot-test an anticipatory counseling intervention detailing unscheduled bleeding and other side effects such as pelvic pain or cramping among new LNG IUS users and compare this with a "control," using video technology. The investigators have chosen video technology for the counseling intervention to ensure that all participants receive the exact same information about LNG side effects, which would be not possible using a face-to-face clinician-participant counseling model.

The investigators propose three phases for this study. In Phase 1, a systematic literature search evaluating effective components in videos used for contraceptive counseling and the development of two separate video scripts will lead to: (1) an intervention, detailing expected side effects and safety of the LNG IUS, and (2) a similar-looking "control," detailing only recommended screening guidelines for women, as well as information about LNG IUS safety. This phase of the study uses focus groups prior to the development of the video interventions, initially with family planning experts for content accuracy and cultural sensitivity, and secondarily with new LNG IUS users for acceptability. Findings from this phase will be used to fine-tune the scripts prior to the development of the videos.

In Phase 2 of the study, the investigators will pilot a trial in the clinical setting to evaluate the anticipatory counseling video intervention and its impact on LNG-IUS knowledge, continuation, health care utilization, and satisfaction. After receiving comprehensive contraceptive counseling from their clinicians, women who choose to have the LNG IUS inserted will be given a brochure that asks them to participate in an online study. After signing-on to an innovative website, participants will be randomized to either an intervention or control video and complete short questionnaires related to demographics, baseline menstruation, satisfaction, and LNG IUS knowledge before and after viewing their assigned video. Women will be followed for six months. They will be asked to complete a short online survey at three and six months regarding LNG IUS continuation, health care utilization, and satisfaction. Findings from this study will serve to design a future, appropriately powered randomized controlled trial assessing LNG IUS continuation, utilization, and satisfaction rates at 12 months.

In Phase 3, we will use the findings from Phase 2 to develop a similar protocol and recruit up to 178 women at three sites across the US to test the same primary aims of the video: LNG-IUS continuation, utilization, and satisfaction over a 12 month period. In phase 3, subjects will be randomized to watch either the control or intervention video.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women aged 18 and over who are deemed appropriate candidates be their healthcare providers and choose to use LNG-IUS, either Mirena or Skyla.
  • Within five days of FIRST using either Mirena or Skyla
  • Willing to answer online questions before and after watching the assigned video (intervention or control)
  • Willing to complete short online questionnaire at three and six months
  • Has working email and/or phone number
  • Able to understand verbal and written English
  • Appropriate LNG-IUS candidates whoa re being treated for other pre-existing medical disorders while using the LNG IUS may continue to take their medications as directed by their healthcare provider.

排除标准

  • Women aged less than 18 years old
  • Initiated LNG-IUS method more than five days from enrollment date.
  • Within six weeks postpartum
  • Breastfeeding
  • Using LNG-IUS for treatment other than contraception
  • Do not have access to the Web
  • Have neither working email or phone number
  • Does not understand written or verbal English
  • Inappropriate candidates for LNG IUS as deemed by healthcare provider

研究组 & 干预措施

Control Video

Sham Comparator

Participants in this study arm will be assigned to watch a short educational video about new pap screening guidelines for women. Intervention: Cancer Screening Guidelines.

干预措施: Cancer Screening Guidelines (Other)

Intervention Video

Active Comparator

Participants in this group will be assigned to watch a short educational video providing anticipatory counseling on their LNG-IUS' side effects and expected changes in bleeding. Intervention: Anticipatory Counseling

干预措施: Anticipatory Counseling (Other)

结局指标

主要结局

Change in LNG-IUS knowledge, satisfaction and continuation from baseline

时间窗: 6 months

Using standardize questionnaires we will assess any significant differences in LNG-IUS knowledge, satisfaction or continuation after 6 months between control arm and intervention arm subjects.

次要结局

  • LNG-IUS user self-reported LNG-IUS healthcare utilization during study period(baseline, 3 months, 6 months)
  • Percent of subjects in Phase II who complete all 3 surveys on-time over 6 months compared by recruitment method and site(6 months)
  • LNG-IUS user self-reported satisfaction with video counseling(6 months)
  • Number of subjects reporting LNG-IUS discontinuation during the study time frame (6 months) by reason for LNG-IUS removal(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Emily Godfrey

Associate Professor, Family Medicine

University of Washington

研究点 (6)

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