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临床试验/NCT02129517
NCT02129517已完成不适用

Oncology Nurse IMPACT: Improving Communication With Patients About Clinical Trials

Case Comprehensive Cancer Center1 个研究点 分布在 1 个国家目标入组 1,262 人开始时间: 2014年11月7日最近更新:
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
1,262
试验地点
1
主要终点
Change in nurse's intention to discuss clinical trials with patients

研究概览

简要总结

This pilot, randomized clinical trial studies a web-based tailored educational program in improving nurse communication with patients about clinical trial treatment options. A web-based tailored educational program may empower and prepare nurses to discuss clinical trial treatment options with patients and may also increase patient participation in clinical trials.

详细描述

PRIMARY OBJECTIVES:

I. To develop and pilot test a theory-driven, web-based, tailored, interactive educational program (Oncology Nurse IMPACT: Improving Communication with Patients about Clinical Trials) for oncology nurses to address barriers to discussing clinical trials with patients.

II. To implement Oncology Nurse IMPACT on a national level and conduct a formal program evaluation.

III. To evaluate the mediators and moderators of education program effect on intentions to discuss clinical trials with patients.

OUTLINE: Participants are assigned to 1 of 2 intervention arms.

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
None

入排标准

性别
All
接受健康志愿者
是

入选标准

  • •Currently practicing nurse
  • •Involved in direct patient care
  • •Self-identify in one of the following primary practice roles--case managers, clinical nurse specialists, nurse practitioners, managers/coordinators, nurse navigators, patient educators, and staff nurses
  • •Available email address

排除标准

  • •Research nurses, nurses without direct patient care, and nurse managers/directors (i.e. not involved in direct patient care)
  • •Lack of email address

研究组 & 干预措施

Arm I (IMPACT Intervention)

Experimental

Oncology nurses watch tailored, web-based informational video clips addressing knowledge, attitudes, subjective norms, and perceived behavioral control (barriers of discussing clinical trials with patients). They also watch role-play video clips to help improve perceived behavioral control and address attitudinal barriers.

干预措施: IMPACT intervention (Other)

Arm I (IMPACT Intervention)

Experimental

Oncology nurses watch tailored, web-based informational video clips addressing knowledge, attitudes, subjective norms, and perceived behavioral control (barriers of discussing clinical trials with patients). They also watch role-play video clips to help improve perceived behavioral control and address attitudinal barriers.

干预措施: survey administration (Other)

Arm II (online educational materials)

Active Comparator

Oncology nurses view online clinical trials educational materials developed based upon NCI clinical trials educational materials for health care providers. The educational materials contain text and tables as presented on the NCI Website.

干预措施: Online education materials (Other)

Arm II (online educational materials)

Active Comparator

Oncology nurses view online clinical trials educational materials developed based upon NCI clinical trials educational materials for health care providers. The educational materials contain text and tables as presented on the NCI Website.

干预措施: survey administration (Other)

结局指标

主要结局

Change in nurse's intention to discuss clinical trials with patients

时间窗: Baseline to 3 months post-intervention

Behavioral intention will be assessed using 4 items (3 with 7 point scales, strongly agree/strongly disagree and 1 which asks for an estimated number of patients). An analysis of covariance (ANCOVA) will be used to compare intention scores, adjusting for the pre-intervention intention score as well as age, ethnicity, education, access to clinical trials, and years spent in nursing as well as other key factors found to be significantly imbalanced between groups.

次要结局

  • Change in knowledge, attitudes, normative beliefs, and perceived behavioral control(Baseline to 3 months post-intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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