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临床试验/NCT06360341
NCT06360341已完成不适用

Feasibility and Acceptability of an Emergency Department Digital Pain Self-Management Intervention to Improve Acute Low Back Pain Outcomes: A Pilot Randomized Controlled Trial

University of Florida2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年4月15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
30
试验地点
2
主要终点
Improving Self-Management Health Outcomes

研究概览

简要总结

The proposed study aims to evaluate a pilot emergency department (ED) digital pain self-management intervention (EDPSI) focused on improving self-efficacy, knowledge, and skills, thus reducing the transition from acute to chronic low back pain in ED patients discharged with axial acute low back pain (aLBP). The proposed research has significant potential to improve self-efficacy (the confidence in one's ability to manage their condition) which is one of the most potent factors for improved health outcomes.

详细描述

Investigators:

Principal Investigator: Alexandria Carey (University of Florida, PhD Candidate) Co-Investigator/ Supervisory Chair: Ann Horgas

Supervisory Committee Members:

  • Laurie Duckworth
  • Hwayoung Cho
  • Jason M. Beneciuk Previous Co-Investigator (2022-2024): Angela Starkweather

IRB #: 202301946

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

盲法说明

Randomization to RC or Intervention group will not be masked to the Principal Investigator (PI), co-PI, or to participants.

入排标准

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

入选标准

  • Patient subjective chief complaint of acute or subacute axial low back pain, low back injury, mechanical low back pain, non-specific low back pain, back sprain, or back strain Or
  • Provider diagnosis of acute axial low back pain
  • ICD-10 discharge codes:
  • Low back pain, unspecified M54.50
  • Pain of lumbar, acute, for less than 3 months; low back strain (S39.012)
  • Unspecific injury of lower back, initial encounter (S39.92XA) And
  • Are aged 18 years and older
  • Can read and consent to participate in the trial
  • Can read and speak English
  • Can complete study follow-up at prespecified intervals
  • Have access to Wi-Fi
  • Have access to a phone or other smart device (e.g. a smartphone, tablet, or computer) that would allow receiving of phone calls, text messages, Zoom meetings, or emails

排除标准

  • Admission to the hospital
  • Disabilities that would inhibit digital intervention learning (medical, psychiatric, traumatic brain injury, concussion, blindness, or deaf)
  • Prisoners/Incarcerated

结局指标

主要结局

Improving Self-Management Health Outcomes

时间窗: 12-weeks

Feasibility and Acceptability of the pilot study will assess recruitment, retention, engagement, satisfaction, and willingness to recommend. Acceptability and intervention satisfaction will be assessed using the Education Preference and Satisfaction Questionnaire (EPSQ) and study satisfaction and recommendation using the Patient Satisfaction and Healthcare Utilization Questionnaire (PSHU). Preliminary Clinical Efficacy will be assessed for self-management, self-efficacy, pain severity and interference. Self-management will be assessed using the short 13-item Patient Activation Measure (PAM), self-efficacy using the Pain Self-Efficacy Questionnaire (PSEQ), pain severity and interference using the Brief Pain Inventory Short-Form (BPI-SF). Preliminary clinical efficacy of the EDPSI for adults with aLBP will be evaluated using estimates of Minimal Clinically Important Difference (MCID), the smallest change in an outcome that patients perceive as meaningful and indicative of improvement.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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