跳至主要内容
临床试验/NCT02704897
NCT02704897已完成不适用

Can a Smartphone-delivered Tool Facilitate the Assessment of Surgical Site Infection, and Result in Earlier Treatment? A Randomized-controlled Trial in Emergency Surgery Patients.

University of Edinburgh4 个研究点 分布在 1 个国家目标入组 492 人开始时间: 2016年6月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
492
试验地点
4
主要终点
Time from surgery to treatment for surgical site infection

研究概览

简要总结

This study aims to evaluate if a smartphone-delivered tool can help assess for wound infections, and if this improves access to care and results in earlier treatment. Participants will be randomised to one of two groups. The intervention group will receive the smartphone-delivered wound assessment tool (SWAT), to access if they have concerns about their wound. The trial period is 30 days.

详细描述

Surgical site infection (SSI) is defined by the Centre for Disease Control and Prevention (CDC) as an infection in the skin and soft tissues of a surgical wound, within 30 days of the operation. It is a common problem, and complicates 2-10% of general surgery operations. The majority of cases are diagnosed outside of hospital and can be treated with oral antibiotics.

Interest in the use of technology in medicine is increasing, with the potential that more advanced technology will help facilitate communication between clinicians and patients, aid in the assessment of patients, and improve clinical decision making. Over two-thirds of people now own smartphones, and regularly use them to access the internet. The investigators wish to use a smartphone delivered questionnaire to help assess SSI and see if this improves access to care and time to treatment.

The investigators will be recruiting emergency surgery patients with smartphones at the Royal Infirmary and Western General Hospitals in Edinburgh.

Participants will be divided into two groups. One group will receive the wound assessment tool, if they are concerned about their wound, they can use the tool to answer a series of questions. If their answers suggest SSI, a clinician will contact them to advise further assessment and treatment. The participants will also be asked to respond to the tool three times during the trial (to collect responses from those without symptoms), and upload photos of their wounds to a secure database.

The second group of participants will receive normal post-operative care.

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
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Emergency Abdominal Surgery Patients
  • Smartphone Owners
  • Able to give valid consent

排除标准

  • Significant visual impairment

结局指标

主要结局

Time from surgery to treatment for surgical site infection

时间窗: Outcome assessed at 30 day follow-up

Measured in days from surgery to commencing antibiotic treatment

次要结局

  • Service Usage(Assessed at 30 day follow-up)
  • Access to Services(Assessed at 30 day follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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