NCT02262429终止不适用
Does a Rapid, Comprehensive Oral Nutritional Supplementation Quality Improvement Program (QIP) Reduce 30-Day Readmission in Malnourished Hospitalized Patients?
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 2,386
- 试验地点
- 4
- 主要终点
- Post-discharge readmissions
研究概览
简要总结
Newly admitted patients will be screened for risk of malnutrition. Patients will receive either the feeding protocol or current oral nutrition supplement (ONS) practice, pending location. Patients will continue the nutrition plan taking the supplement post discharge. Study team will follow-up with telephone calls to help support post-discharge ONS compliance. Quality and service utilization data will be gathered for analysis.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- •Patient is ≥ 18 years of age.
- •Patient is screened for malnutrition with an MST score ≥ 2 (see Appendix C).
- •Patient has length of stay of hospital stay > 2 days.
- •Patient is able to consume foods and beverages orally.
- •Patient receives Ensure, Nepro or Glucerna during the course of his or her hospital stay in connection with the QIP.
排除标准
- •Patient is pregnant.
- •Patient is intubated, receiving tube feeding or parenteral nutrition.
- •Patient unable to provide HIPAA authorization and informed consent.
- •Patient is discharged to hospice care.
- •Patient has a condition that would preclude ingestion / absorption of the oral nutritional supplements, including allergic response to any ONS ingredient.
- •Patient has severe dementia or delirium, brain metastases, eating disorder, history of significant neurological or psychiatric disorder.
- •Patient has stated an allergy or intolerance to any of the ingredients in the study products.
结局指标
主要结局
Post-discharge readmissions
时间窗: November 2014 - April 2015, 30 days post discharge
Non-elective readmission 30 days post discharge.
次要结局
- Hospital length of stay(October 2014 - March 2015, up to 6 months)
研究者
研究点 (4)
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