跳至主要内容
临床试验/NCT04576715
NCT04576715已完成不适用

Promoting Recovery in Children Who Sustain a Mild Traumatic Brain Injury: mTBI Evaluation and Management (TEaM)

Emory University3 个研究点 分布在 1 个国家目标入组 101 人开始时间: 2022年8月19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
101
试验地点
3
主要终点
Time to return to full activity post injury

研究概览

简要总结

The purpose of this study is to evaluate a multi-disciplinary, multi-setting intervention with the goal of improving outcomes for children who have experienced a mild traumatic brain injury (mTBI). The project aims to improve and support mTBI diagnosis and management, and improve critical decision making by clinicians during their interaction with the injured child, their family, and their school.

详细描述

Emergency, urgent care, and primary care providers participating in the study will be block randomized in a 1:1 ratio by practice type to receive the intervention or continue with their standard practice. All enrolled clinicians (both trained and control providers) patients they care for will be screened for inclusion in the trial.

Additionally, a pre/post intervention will be layered upon the randomized educational intervention to evaluate the effects of the information technology decision support tool (i.e. eMR) in isolation of the clinician education intervention. The 32-month mTBI patient enrollment period will be divided into two 16 months segments. The first 16 months will be without the eMR intervention being visible, and the remaining 16 months post eMR screening and decision support deployment in the ED and UC. This study design allows us to evaluate the independent and interactive effects of the decision support tool and educational intervention.

Enrolled children will be followed for up to three months post injury to ascertain the effect of the interventions on the primary aim (reduction of school problems/performance) and secondary aims.

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
None

入排标准

年龄范围
5 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • PROVIDER INCLUSION CRITERIA
  • Actively practicing physician or APP in the CHOA System
  • Primary practice in either ED, UC, and/or PCP

排除标准

  • Inability or unwillingness to provide written/electronic informed consent
  • Unable to fulfill study training / education requirements
  • CHILD INCLUSION CRITERIA - RETROSPECTIVE
  • School age (5-18 yoa)
  • Evaluated in ED / UC / PCP within 72 hours of injury
  • Discharged home from ED / UC / PCP (e.g., not admitted to hospital)
  • CHILD EXCLUSION CRITERIA - RETROSPECTIVE
  • Non-English speaking
  • Known severe developmental delay or known severe psychiatric history
  • Known prior severe brain injury
  • Known mTBI within past 3 months
  • First mTBI visit outside of CHOA network
  • CHILD INCLUSION CRITERIA - PROSPECTIVE
  • Meets above inclusion for retrospective portion plus:
  • mTBI likely present as defined by:
  • Positive diagnosis by clinician or mTBI OR
  • Positive triage screen plus positive symptom checklist
  • CHILD EXCLUSION CRITERIA - PROSPECTIVE
  • Does not meet above exclusion for retrospective portion plus:
  • Requests to Opt-Out via e-mail or first phone contact
  • Inability or unwillingness to provide verbal informed telephone consent/assent

研究组 & 干预措施

TEaM Intervention Group

Experimental

Dedicated Provider Education plus Information Technology Support. The IT support includes addition of an eMR concussion screening, followed by an alert to the provider, followed by a structured assessment / evaluation template.

干预措施: TEaM Intervention (Behavioral)

Control Group

Active Comparator

Standard medical protocol for the management of mTBI in children. This group will not receive interventional Provider Training on the TEaM concussion evaluation examination and utilization of the eMR template.

干预措施: Standard of Care (Behavioral)

结局指标

主要结局

Time to return to full activity post injury

时间窗: Up to 3 months post-intervention

Measured by serial PCSI and return to activity. PCSI Total score (PPCS-Persistent Post-Concussive Symptoms - will be calculated via the PCSI Total Score with scores classified as "Recovered" or "Non-Recovered (PPCS)" based on the Reliable Change Metrics that reflect recovery or not (e.g., for Parent and Adolescent PCSI Total RAPID score \<5 indicates symptom recovery). Total score ranges from 0 to 100%. Lower % with PPCS in Intervention group compared to Control indicates better study outcome.

Change in CLASS survey score

时间窗: 1 week, 2 week and 1 month post return to school

Concussion Learning Assessment and School Survey (CLASS), identifies the types of problems students experienced across all grades. Total score range 0-42 (14 individual items rated 0-3, 0 = no problem, 3 = significant problem). Higher score reflects a greater problem/ worse outcome.

Change in Peds-QL score

时间窗: 1 week, 2 week and 1 month post return to school

Pediatric Quality of Life (PedsQL) scale, includes 23 items, rated 0-4 (assesses different areas of function (physical, emotional, social, school) to determine if the child is having any problems with various tasks in each functional area and if so, how often the difficulty occurs). 4 sub scales (general health 8 items 0-4 scaling, 0-32 total; social 5 items, 0-4 scaling, 0-20; school 5 items, 0-4 scaling, 0-20; emotional 5 items, 0-4 scaling, 0-20, 0=it is never a problem, 4= it is almost always a problem). Higher raw score reflects worse overall quality of life. Items are calculated and transformed into an overall score with a range of 0-to-100 points, with 100 points indicating better HRQoL.

Post-concussion symptom inventory (PCSI) total score at 3 months post injury

时间窗: 3 months post injury

Persistent post-mTBI symptoms as measured by the PCSI total score at 3 months post injury. Total score range, 0-24 (4 symptoms on a 0-6 scaling). Higher score reflects a greater problem/worse outcome.

Change in Post-concussion symptom inventory (PCSI) total score

时间窗: 1 week, 2 week and 1 month post return to school

Change in Post-concussion symptom inventory (PCSI). Total score range, 0-24 (4 symptoms on a 0-6 scaling). Higher score reflects a greater problem/worse outcome.

次要结局

  • Primary Care Physician (PCP) follow up visits(3 months post-intervention)
  • Number of letters sent to school(2 weeks post-injury)

研究者

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

David Wright

Professor

Emory University

研究点 (3)

Loading locations...

相似试验