跳至主要内容
临床试验/NCT06069011
NCT06069011已完成不适用

Improving Access to Quality Care for Children and Adolescents Presenting to the Pediatric Emergency Department With Musculoskeletal Problems: a Pilot Randomized Control Trial

McGill University Health Centre/Research Institute of the McGill University Health Centre2 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2023年9月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
66
试验地点
2
主要终点
Rate of consent

研究概览

简要总结

The goal of this clinical trial is to compare two methods of managing low acuity musculoskeletal complaints in children and adolescents ages 6 to 17.99 years in the pediatric emergency department. The main question it aims to answer is whether delivering care in two methods is feasible. Participants will receive care while in the emergency department and will be followed for a period of 1-month post-presentation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
6 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • aged 6.00-17.99 years of age
  • present to the Montreal Children's Hospital Emergency Department with a suspected MSK complaint, traumatic or not
  • are given a triage score of 3 (urgent), 4 (less urgent), or 5 (nonurgent) according to the Canadian Triage and Acuity Scale (CTAS)
  • are able to communicate in French or English

排除标准

  • present with a major MSK condition requiring urgent care (e.g., open fracture, open wound)
  • a red flag (e.g. progressive neurological disorder, infectious symptoms)
  • a co-morbid unstable condition.

结局指标

主要结局

Rate of consent

时间窗: through study completion an average of 4 weeks post-enrolment

rate of consented patients related to patients approached rate of randomization, feasibility of administration of outcomes

Completed outcome measures

时间窗: through study completion an average of 4 weeks post-enrolment

proportion of participants who complete all outcome measures

次要结局

  • Pain intensity on faces rating scale(through study completion an average of 4 weeks post-enrolment)
  • Pain interference with function PROMIS scale(through study completion an average of 4 weeks post-enrolment)

研究者

发起方
McGill University Health Centre/Research Institute of the McGill University Health Centre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Isabelle Gagnon

Senior Investigator

McGill University Health Centre/Research Institute of the McGill University Health Centre

研究点 (2)

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