跳至主要内容
临床试验/NCT02698332
NCT02698332已完成不适用

Effect of a Diagnostic Algorithm for Urinary Tract Infection on Appropriate Use of Antibiotics and Diagnostics in General Practice - a Cluster Randomized Trial

University of Copenhagen1 个研究点 分布在 1 个国家目标入组 1,550 人开始时间: 2016年3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
入组人数
1,550
试验地点
1
主要终点
Difference in appropriate primary choice of treatment in the two groups.

研究概览

简要总结

The aim of this study is to investigate the effect of diagnostic algorithm for urinary tract infection (UTI) on appropriate prescribing of antibiotics and use of diagnostics for patients with symptoms of urinary tract infection consulting their general practitioner.

70 general practices participating in an observational study regarding UTI are randomized to either receiving a diagnostic algorithm or not receiving anything additional.

The study is observational on the patient level and interventional on the practice level.

详细描述

STUDY DESIGN AND SETTING Cluster randomized controlled single blinded study of a diagnostic aid in general practice RECRUITMENT OF GENERAL PRACTICES Recruitment of general practices was done through online advertisement in email newsletters for general practice, invitation by post of 200 practices and invitation of 44 general practices already participating in a medical audit project regarding UTI (ref til Gloria). Only practices in the Capital Region of Denmark could participate.

RANDOMIZATION AND BLINDING Randomization was performed using an online random number generator and an employee not part of the investigation team sent out the diagnostic algorithm to the intervention group. The practices were asked not to reveal their allocation to the investigators in case of contact. Allocation was concealed to the investigators until after analysis of the primary outcomes.

INTERVENTION AND CONTROLS The practices in the intervention group received a laminated diagnostic algorithm by post and got access to a smart-phone integrated web-page, which could calculate post-test probabilities based on pre-test probabilities and accuracy of diagnostic tests .The diagnostic algorithm consists of three parts, one about urine dipstick, one about point-of-care microscopy and one about urine culture . The practices were instructed, use of the algorithm was voluntary. Control practices did not receive a diagnostic algorithm and did not have access to the smart-phone integrated web-page.

RECRUITMENT OF PATIENTS The practices were told to register diagnostics and treatment on the first 20-40 patients presenting in general practice with symptoms of UTI regardless of age, sex and comorbidity. For each patient, the practice sent a urine sample to the microbiological department as reference.

INCLUSION AND EXCLUSION CRITERIA Inclusion criteria were all patients with symptoms of UTI who had not formerly participated in the study and where urinalysis was performed. The only exclusion criterion was acute admission to hospital.

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
Double (Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •All patients presenting in general practice with symptoms of UTI who has not formerly participated in the study.

排除标准

  • •Acute admission to hospital.

研究组 & 干预措施

Algorithm for UTI

Active Comparator

Practices in this groups receives a diagnostic algorithm for UTI by post

干预措施: Algorithm for UTI (Device)

Control

No Intervention

Practices in this group does not receive anything in addition to instructions in the observational registration.

结局指标

主要结局

Difference in appropriate primary choice of treatment in the two groups.

时间窗: 3 months

Difference in price of point-of-care diagnostics used in the two groups

时间窗: 3 months

次要结局

  • Difference in appropriate choice of treatment on the day after consultation (day ) in the two groups(3 months)
  • Difference in correct decision to treat on the day of consultation (day 1) in the two groups(3 months)
  • Difference in appropriate final choice of treatment in the two groups.(3 months)
  • Difference in appropriate choice of treatment on the day of consultation (day 1) in the two groups(3 months)
  • Difference in correct decision to treat on the day after consultation (day 2) in the two groups(3 months)
  • Number of diagnostics used in the two groups(3 months)
  • Practice satisfaction with participation in the project in the two groups(4 months)
  • Practice acceptance of the algorithm in the intervention group(4 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Anne Holm

MD PhD-fellow

University of Copenhagen

研究点 (1)

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