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临床试验/NCT03629509
NCT03629509Unknown不适用

Implementation of the Begin Exploring Fertility Options, Risks and Expectations (BEFORE) Decision Aid - A Stepped Wedge Cluster Randomized Trial

Unity Health Toronto2 个研究点 分布在 1 个国家目标入组 224 人开始时间: 2018年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
224
试验地点
2
主要终点
Patient-reported outcome questionnaire - Fertility Preservation Questionnaire

研究概览

简要总结

Fertility is of great importance to young women with cancer. Concerns about the ability to become pregnant after cancer treatment may influence treatment decisions and fertility decision-making is challenging. Despite these challenges, there is a lack of fertility decision support tools. Our team developed the Begin Exploring Fertility Options, Risks and Expectations (BEFORE) decision aid for young breast cancer patients in Canada. This study aims to evaluate the implementation of the BEFORE decision aid in hospital settings through a stepped wedge cluster randomized trial.

详细描述

The investigators will conduct a stepped wedge cluster randomized trial to sequentially implement the BEFORE decision aid in clinical settings that are currently recruiting young breast cancer patients for the Reducing the bUrden of Breast cancer in Young women (RUBY) Study (www.womensresearch.ca/ruby-study/).

For this trial 24 participating RUBY sites were grouped into 14 clusters (1 to 3 sites per cluster). The decision aid intervention will be sequentially rolled out over the course of 48 weeks to all clusters. None of the clusters will be switched from control to intervention during the first 6 weeks of the study to establish a baseline. Then two clusters will move from the control to the intervention every 6 weeks (called a 'step'). There will be 7 steps total during the study period. At the end of the 7th step all clusters (i.e., participating RUBY sites) will have received the decision aid intervention. The time-point of when the clusters will be switched from control to intervention will be randomized.

The data collection includes obtaining secondary data collected as part of the RUBY study from all patient participants who were enrolled in RUBY during the study period. The primary outcome is the number of patients reporting that fertility tools were recommended to them, based on RUBY participant responses to a 3-month fertility questionnaire. The investigators hypothesizes that following the implementation of the decision aid intervention a 20% difference will be observed, from 10% in the control to 30% in the intervention, in the number of patients who report that someone in their care team recommended a fertility tool.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Young females diagnosed with histologically-confirmed breast cancer will be eligible to participate if they:
  • are age =18 years and prior to their 41st birthday;
  • are able to provide verbal informed consent and complete the interviews in English or French;
  • completed the 3-month fertility questionnaire as part of the RUBY Study.

排除标准

  • 未提供

研究组 & 干预措施

Pre-Intervention

Other

The BEFORE decision aid will be available for use on the RUBY communication portals (Twitter, Facebook and study portal)

Data will be collected 6 weeks before the implementation of the BEFORE decision aid in RUBY sites to establish a baseline

干预措施: BEFORE decision aid (Behavioral)

BEFORE Decision Aid Intervention

Experimental

Evaluate more intensive strategies to promote use of the BEFORE decision aid through:

  1. We will advertise the availability of the BEFORE decision aid with posters placed in clinic areas at each RUBY site, and will have small handouts available to be distributed in clinic.
  2. We will conduct an educational intervention describing and promoting the use of the BEFORE decision aid and general oncofertility information to nurses and support staff at each RUBY site. This will include an optional 1hr informational webinar, direct outreach and training of nurses/support staff on the use of the tool.

干预措施: BEFORE decision aid (Behavioral)

Post-Intervention

Other

Data will be collected after the BEFORE decision aid has been implemented in each RUBY site regarding the recommendation of fertility resources, most useful/least useful tool, and use of the BEFORE decision aid.

干预措施: BEFORE decision aid (Behavioral)

结局指标

主要结局

Patient-reported outcome questionnaire - Fertility Preservation Questionnaire

时间窗: 3 months from date of randomization

Number of patients reporting that fertility tools were recommended to them following their breast cancer diagnosis

次要结局

  • BEFORE decision aid online survey - Provider Recommendation of Decision Aid(From date of randomization until the end of the study at 48 weeks)
  • BEFORE decision aid online survey - Patient Learning About Decision Aid(From date of randomization until the end of the study at 48 weeks)
  • BEFORE decision aid online survey - Patient Satisfaction(From date of randomization until the end of the study at 48 weeks)

研究者

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

Nancy Baxter

Chief of General Surgery, Scientist

Unity Health Toronto

研究点 (2)

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