Dissemination and Implementation of DIGEST™ as an Evidence-based Measurement Tool for Dysphagia: A Randomized Implementation Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 85
- 试验地点
- 1
- 主要终点
- Adoption of DIGEST in routine clinical documentation for oncology MBS studies
研究概览
简要总结
To improve swallowing outcomes in cancer through clinical implementation of the Dynamic Imaging Grade of Swallowing Toxicity (DIGEST™) as an evidence-based practice (EBP) tool to grade pharyngeal dysphagia (difficulty swallowing) as a toxicity of cancer.
详细描述
Primary Objective Assess the impact of implementation strategies on clinical adoption (reach) of DIGEST for oncology MBS studies.
Secondary Objective Assess the impact of implementation strategies on the fidelity (reliability) of DIGEST adoption for oncology MBS studies
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •A hospital or clinic affiliated with the Veteran's Affairs system, University of Wisconsin system, or Ohio State University system.
- •A minimum average of 10 Modified Barium Swallow (MBS) procedures per month in oncology patients in preceding year.
- •MBS imaging files are recorded and archived as a routine procedure (and accessible to researchers).
排除标准
- 未提供
研究组 & 干预措施
Control Arm 1
The control arm will receive no active implementation strategy.
干预措施: No intervention (Other)
Training Arm 2
Represents a low intensity implementation strategy solely using the DIGEST training program as the intervention.
干预措施: DIGEST Training Program (Other)
Training + Practice Facilitation Arm 3
Represents a higher intensity strategy using the same training program plus practice facilitation.
干预措施: DIGEST Training + Practice Facilitation (Other)
结局指标
主要结局
Adoption of DIGEST in routine clinical documentation for oncology MBS studies
时间窗: Through study completion; an average of 1 year
次要结局
未报告次要终点