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临床试验/NCT02721706
NCT02721706已完成不适用

Cost-effectiveness Study of the CIPA Screening Method for Patients With Nutritional Risk at Hospital Admission

University Hospital of the Nuestra Señora de Candelaria2 个研究点 分布在 1 个国家目标入组 823 人开始时间: 2015年1月1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
发起方
入组人数
823
试验地点
2
主要终点
Cost-effectiveness measured by incremental Cost-effectiveness ratio (ICER)

研究概览

简要总结

Objectives: To evaluate the cost-effectiveness of implementing a malnutrition screening tool "CIPA" at the Hospital Universitario Nuestra Señora de la Candelaria (HUNSC), comparing the impact on health and the healthcare costs of hospitalised patients who are screened for malnutrition and of patients following standard clinical practice. Methodology: The study will consist of a controlled trial on patients admitted to the Internal Medicine and General and Digestive Surgery wards at the HUNSC. In both wards patients will be assigned to a control or to an intervention group. The control group will follow usual hospital clinical care, while the intervention group will be administered the screening tool "CIPA" for early detection of malnutrition cases and they will be treated according to the screening results. The following variables will be evaluated: length of stay in hospital, mortality, readmissions and in-hospital complications. Cost-effectiveness analysis will be undertaken measuring effectiveness by Quality-Adjusted Life Years (QALYs). Cost per patient will be measured by identifying health care resource utilisation, and the cost-effectiveness measure will be the Incremental Cost-Effectiveness Ratio (ICER). Investigators will calculate the incremental cost per QALY gained related to the intervention. This analysis will allow to quantify the costs (incurred and saved) related to the introduction of the malnutrition screening tool CIPA in the hospital context and to measure the health impact of screened patients.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Screening
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

入选标准

  • Formal consent to participate in the study.
  • Patients admitted to the Internal Medicine or General Surgery wards.

排除标准

  • Patients treated with nutritional support before CIPA screening is performed.
  • Patients transferred from other wards.
  • Patients with an expected length of stay less than 72 hours.
  • CIPA screening unfeasible for any reason.
  • Patients with poor short-term prognosis.
  • Bed destination at hospital admission nonrandomized.
  • Patients participating in other investigation study.
  • Pregnancy

研究组 & 干预措施

CIPA screening tool

Experimental

Patients are evaluated by CIPA nutritional screening tool

干预措施: CIPA nutritional screening tool (Other)

usual hospital clinical care

No Intervention

Patients are not subject of CIPA screening tool, and continue the usual hospital clinical care

结局指标

主要结局

Cost-effectiveness measured by incremental Cost-effectiveness ratio (ICER)

时间窗: up to 3 months after Hospital discharge time

次要结局

  • incidence of readmissions(up to 3 months after hospital discharge time)
  • Quality of life measured by quality-adjusted life years (QALYs)(up to 3 months after Hospital discharge time)
  • mean length of stay (days)(through study completion, an average of 13 days)
  • incidence of mortality(up to 3 months after Hospital discharge time)

研究者

发起方
University Hospital of the Nuestra Señora de Candelaria
申办方类型
Other
责任方
Principal Investigator
主要研究者

José Pablo Suárez Llanos

Ph.D, M.D.

University Hospital of the Nuestra Señora de Candelaria

研究点 (2)

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