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临床试验/NCT01721200
NCT01721200已完成不适用

"Learning About Biologics"

Geisinger Clinic2 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2012年11月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
125
试验地点
2
主要终点
The Proportion of Subjects Who Are Classified as Having Made an Informed Value Concordant Choice at 2 Weeks

研究概览

简要总结

This study is a randomized controlled trial designed to examine the efficacy of an educational decision support tool for patients with rheumatoid arthritis who continue to have active disease despite use of traditional disease modifying drugs. The study will take place at Geisinger Medical Center in Danville, PA. Eligible subjects will be identified by the treating physician and those providing consent will be randomized to usual care versus use of the decision support tool.

详细描述

Data suggest that undertreatment of rheumatoid arthritis (RA) patients may be in part due to inadequate decision support when they face whether or not to start biologic therapy. No proven way exists to inform or support RA patients who are candidates for biologic therapy. Communicating information about biologic medication is particularly challenging because of the sheer number of risks to disclose, the difficulty explaining the risks of extremely rare adverse events (AEs), and the tendency for people to discount (or underweight) future benefits.

Dr Liana Fraenkel at Yale University is the Primary Investigator and developer of this theory-based high quality decision support tool to effectively inform RA patients who are candidates for biologics. Dr. Eric Newman will be Principal Investigator for the project which will be conducted at Geisinger Medical Center. All subjects enrolled will complete a baseline survey and then will be randomized to use of the decision support tool or to usual care. Those randomized to usual care will be offered the opportunity to access the tool once enrollment is closed and all follow-up visits have been completed.

Outcomes will be assessed at two and six weeks after the baseline visit by the Geisinger Telephone Survey and Interviewing Facility. This facility is equipped with 12 computers and runs two shifts a day. The Survey Unit uses a state-of-the-art Windows based Computer Assisted Telephone Interview (CATI) system to administer surveys and collect research data. The group holds 12 interviewer licenses for the CATI system. Trained and experienced interviewers are available to make the calls from 9 am to 9 pm Monday through Friday and from 10 am to 2 pm on Saturdays.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects must be at least 18 years of age
  • Able to speak and read English
  • Meet the revised American College of Rheumatology criteria for the diagnosis of RA
  • Have active disease warranting initiation of a new biologic (or small molecule if and when FDA-approved) therapy as determined by their rheumatologist

排除标准

  • Fail to meet the inclusion criteria
  • Have a current infection
  • Have cancer of any type diagnosed within the past five years (except non-melanoma skin cancer)
  • Have a history of lymphoma, leukemia, or melanoma
  • Have a chronic inflammatory disease (in addition to rheumatoid arthritis) requiring treatment with immunosuppressive medications
  • Have chronic liver disease due to hepatitis C or B
  • Are HIV positive
  • Have a positive screening test for tuberculosis (tuberculin skin test or interferon-gamma release assay) or radiographic lesions suggestive of inactive tuberculosis and have not completed an adequate course of chemoprophylactic therapy
  • Are hearing or visually impaired
  • Are scheduled for surgery

研究组 & 干预措施

Decision Support Tool

Other

This study will examine the efficacy of a web-based educational decision support tool.

干预措施: Decision Support Tool (Other)

Usual Care

Other

Usual Care Group will receive their biologic drug teaching from their rheumatologist.

干预措施: Usual Care (Other)

结局指标

主要结局

The Proportion of Subjects Who Are Classified as Having Made an Informed Value Concordant Choice at 2 Weeks

时间窗: 2 weeks

We classified subjects as having made an informed choice to escalate care if they answered at least 75% of the knowledge questions correctly and had low decisional conflict as defined by a score of 25 or lower on the combined subjective knowledge and values clarity subscales.

次要结局

  • To Test Uptake(8 weeks)
  • Changes in Willingness(8 weeks)
  • To Test Screening and Recruitment Procedures(8 weeks)
  • Acceptability to Physicians(8 weeks)
  • Changes in Perceived Knowledge(8 weeks)
  • Patient-physician Communication(8 weeks)
  • Use of Biologics(8 weeks)
  • To Test Adherence to the Intervention(8 weeks)
  • Changes in Knowledge(8 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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