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临床试验/NCT03892850
NCT03892850Unknown不适用

Effectiveness and Safety of the Nursing Prescription in Acute Health Problems of Low Complexity. Randomized Clinical Trial

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina0 个研究点目标入组 374 人开始时间: 2019年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
374
主要终点
no re-attendance during the following 72 hours

研究概览

简要总结

Objective: To compare the efficacy/effectiveness of pharmacological nurse prescription with medical prescription in patients attended in a primary care center for minor acute health problems.

Scope of the study: Multicenter study, with the participation of 8 primary care centers of Catalonia.

Methodology: Randomized blind clinical trial, with experimental group receiving pharmacological nurse prescription and a control group receiving medical prescription. Subjects are individuals who request a same day consultation for minor acute pathologies and meet the selection criteria, with random assignment of 374 subjects, 187 per group.

The efficacy/effectiveness of the prescribed treatment will be considered as a no re-attendance during the following 72h and will be completed with the variables: information and knowledge of the treatment, adverse effects, compliance, satisfaction level and resolution of the health problem. The data collection is done 10 days after the visit by an ad-hoc telephone questionnaire of 11 items, previously tested. The analysis is done using the SPSS software version 21.0, obtaining data of descriptive, multivariate and inferential statistics.

Implications for practice: To evidence the equivalence of pharmacological nurse prescription with medical prescription for minor acute health problems

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Contusion
  • •Diarrhea / vomit
  • •Fever without focality
  • •Urinary distress
  • •Odinophagy
  • •Toothache
  • •Skin Bite
  • •Upper respiratory symptoms
  • •Ankle twist

排除标准

  • •Language barrier
  • •Cognitive deterioration
  • •Sensory deficit
  • •Pregnancy
  • •Immunosuppression
  • •Neoplasia in the last 5 years
  • •Does not participate / Does not sign consent
  • •Breastfeeding period
  • •Reconsult
  • •Resides outside of Spain
  • •Treatment with glucocorticoids in the last 6 months

研究组 & 干预措施

nurse prescription

Experimental

experimental group receiving pharmacological nurse prescription

干预措施: Nurse prescription (Behavioral)

medical prescription

Active Comparator

control group receiving medical prescription

干预措施: Medical prescription (Behavioral)

结局指标

主要结局

no re-attendance during the following 72 hours

时间窗: During next 72 hours

Options: Yes / No

次要结局

  • satisfaction level(after 10 days)
  • compliance(after 10 days)
  • resolution of the health problem(after 10 days)
  • Level of information and knowledge of the treatment(after 10 days)
  • adverse effects(after 10 days)

研究者

发起方
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
申办方类型
Other
责任方
Sponsor

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