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临床试验/NCT07225023
NCT07225023尚未招募不适用

A Multi-Site Feasibility Trial of Embedded Emergency Department Physical Therapy for Dizziness

Northwestern University2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年12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
尚未招募
入组人数
100
试验地点
2
主要终点
Longitudinal participant surveys (effectiveness): screening-to-enrollment ratio

研究概览

简要总结

This is a multi-site feasibility trial of an embedded emergency department (ED) physical therapy care model for dizziness at two EDs in the Northwestern Medicine and University of Utah Health systems. The study intervention (embedded ED physical therapy) is a reconceptualization of the traditional outpatient physical therapy care model in which we place a physical therapist directly in the ED to initiate timely care for patients with dizziness; we previously evaluated this intervention in a single center randomized trial for low back pain. This multi-site feasibility trial will be comprised of 9 months of active intervention and 12 months of longitudinal data collection. The two sites will be parallel randomized 1:1 to receive either the embedded ED physical therapy condition (intervention, n=1) or usual care (control, n=1) via simple randomization. This trial focuses on feasibility outcomes - such as our ability to enroll participants, deliver the intervention with fidelity, and collect longitudinal patient-reported outcome data and electronic health record data.

详细描述

After a 12-month milestone-driven planning and preparation phase, we will conduct a 21-month randomized feasibility clinical trial of the embedded ED physical therapy intervention at the Northwestern Medicine and University of Utah health systems, comprised of 9 months of active intervention and 12 months of longitudinal data collection. Two hospital EDs (Northwestern Memorial Hospital, University of Utah Hospital) will be randomized to receive either the embedded ED physical therapist intervention (treatment, n=1) or usual care (control, n=1). Following completion of the feasibility trial, the control site will receive the intervention as per standard waitlist procedures for randomized trials. A third hospital ED (Northwestern Lake Forest Hospital) will not participate in randomization or participant enrollment but will contribute baseline electronic health record data to assist in feasibility assessments for a future full-scale trial.

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

入选标准

  • •Emergency Department (ED) visit with primary diagnosis related to dizziness
  • •ED visit occurring at an ED site participating in randomization (Northwestern Memorial Hospital, University of Utah Hospital)
  • •ED visit check-in time during the hours of 8am-8pm
  • •Age greater than or equal to 18 years; there is no age maximum
  • •English or Spanish-speaking

排除标准

  • •Severe neurologic deficit concerning for ischemic or hemorrhagic stroke (i.e., that would necessitate activating a stroke code)
  • •Currently in police custody
  • •Unable to consent
  • •Known pregnancy

研究组 & 干预措施

Embedded Emergency Department Physical Therapy

Experimental

We place a physical therapist directly in the emergency department to initiate timely care for patients with dizziness rather than waiting on an outpatient referral to physical therapy, which can often take weeks to accomplish, if ever at all. The actual techniques and approaches used by the embedded ED physical therapist in this study (e.g., exercises, maneuvers, coaching) are standard-of-care and do not involve investigational interventions, devices, or drugs.

干预措施: Embedded Emergency Department Physical Therapy (Other)

Usual Care

Other

Usual care treatment for dizziness presenting in the emergency department (ED). Usual care consists of any ED testing or treatment not involving an ED physical therapist in accordance with the treating physician's usual and customary practice. This could include diagnostic imaging, patient education and resources, and administration and/or prescribing of medications.

干预措施: Usual Care (Other)

结局指标

主要结局

Longitudinal participant surveys (effectiveness): screening-to-enrollment ratio

时间窗: Baseline

Number of participants who enter screening compared to the number of participants who enroll in the study. Variable type: binary / proportion.

Longitudinal participant surveys (effectiveness): participant retention rate defined as completion of at least one follow-up survey.

时间窗: 12 months

Ratio of participants enrolled to the number who complete at least one follow-up survey.

Electronic Health Record (EHR) extraction (implementation): adoption of Emergency Department (ED) physical therapy

时间窗: Baseline

Adoption is defined as the number of potentially eligible dizziness ED visits have a documented order for a physical therapy evaluation. Cross-sectional at the level of site/Emergency Department during the trial. Variable type: Proportion.

Longitudinal participant surveys (effectiveness): missing data rate for the Dizziness Handicap Inventory

时间窗: 12 months

Rate of missing data for assessments administered between baseline and 12 months. Variable type: binary / proportion.

Electronic Health Record (EHR) extraction (implementation): fidelity of Emergency Department (ED) physical therapy

时间窗: Baseline

Fidelity is defined as the number of dizziness ED visits that have a structured research note documenting use of the protocol. Cross-sectional at the level of site/Emergency Department (ED) during the trial. Variable type: proportion.

Clinician surveys before and after implementation of the intervention (implementation): Normalisation Measure Development Questionnaire (NoMAD) questionnaire scores

时间窗: 1-6 months prior to opening study to accrual and 1-6 months after the last participant enrolls at the site.

1-6 months prior to opening study to accrual and 1-6 months after the last participant enrolls at the site. Variable type: continuous.

次要结局

  • Longitudinal participant surveys (effectiveness): a sum of the missing data rate for the remaining Participant Reported Outcomes (PROs) combined.(12 months)
  • Electronic Health Record (EHR) extraction (effectiveness): rate of subsequent health care encounters.(12 months)
  • Electronic Health Record (EHR) extraction (effectiveness): rate of prescribing sedating medications (including antihistamines and benzodiazepines)(12 months)
  • Electronic Health Record (EHR) extraction (effectiveness): rate of advanced diagnostic imaging(12 months)
  • Clinician surveys before and after implementation of the intervention (implementation): Acceptability of Intervention Measure (AIM)(1-6 months prior to opening study to accrual and 1-6 months after the last participant enrolls at the site.)
  • Clinician surveys before and after implementation of the intervention (implementation): Intervention Appropriateness Measure (IAM)(1-6 months prior to opening study to accrual and 1-6 months after the last participant enrolls at the site.)
  • Clinician surveys before and after implementation of the intervention (implementation): Feasibility of Intervention measure (FIM).(1-6 months prior to opening study to accrual and 1-6 months after the last participant enrolls at the site.)

研究者

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

Howard Kim

Associate Professor

Northwestern University

研究点 (2)

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