跳至主要内容
临床试验/NCT07375914
NCT07375914招募中不适用

Comprehensive Biopsychosocial Approach for Acute Low Back Pain Management in the Emergency Department: a Stepped-wedge Cluster-randomized Clinical Trial

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 782 人开始时间: 2026年4月14日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
782
试验地点
1
主要终点
Pain Interference Score at 7 days

研究概览

简要总结

Acute low back pain, the second leading cause of medical consultations in France, poses a major public health challenge, particularly because of its high risk of progressing to chronic low back pain-the leading cause worldwide of years lived with disability. Pharmacological treatments such as paracetamol, opioids, non-steroidal anti-inflammatory drugs (NSAIDs) and muscle relaxants show limited benefit in terms of pain intensity or functional disability. Non-pharmacological treatments, including exercise therapy and psychological support, show promising results but remain hampered by methodological biases and small sample sizes.

A biopsychosocial approach that combines pharmacological treatments, physical therapy, psychological support and social interventions has demonstrated moderate improvements in pain and function for chronic low back pain but remains insufficiently studied for acute presentations. French guidelines advocate a combined strategy involving paracetamol, NSAIDs, physical activity and psychosocial risk assessment. However, a French multicentre retrospective study highlighted marked heterogeneity in clinical practice, along with a low adoption rate (<10 %) of these recommendations in emergency departments, underscoring the need to strengthen adherence to evidence-based management strategies. We hypothesise that a multimodal intervention targeting physicians (guideline reminders) and patients (information on disease progression and multidisciplinary care plans), to enable the systematic implementation of all aspects of a biopsychosocial approach in emergency departments, could reduce short-term pain and disability in patients with acute low back pain.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged 18 to 55 presenting to a participating emergency department, and
  • Presenting with acute non-traumatic low back pain, newly developed or worsened within the past 7 days.
  • Moderate to severe pain, defined as a score of ≥4 on a 0-10 numerical rating scale.
  • Provision of informed consent after being given the information sheet.
  • Patients covered by social security (excluding AME).

排除标准

  • Presence of a 'red flag' according to HAS guidelines, including: motor neurological deficit or cauda equina syndrome, non-mechanical pain, trauma, active neoplastic disease or history of inflammatory rheumatism, suspected osteoarticular infection, recent spinal surgery with worsening symptoms, suspected acute vascular pathology, prolonged use of medications or corticosteroids, significant structural spinal deformity, or deterioration of general health.
  • Inability to attend the 3-month follow-up.
  • Poor command of French.
  • Patient under guardianship/curatorship or deprived of liberty.
  • Pregnant or breastfeeding women

研究组 & 干预措施

Control group

No Intervention

Usual care - Standard care for acute non-specific low back pain at clinician's discretion

Intervention group

Experimental

Biopsychosocial approach

干预措施: Biopsychosocial intervention (Other)

结局指标

主要结局

Pain Interference Score at 7 days

时间窗: 7 days

Pain interference score at 7 days, assessed using the Pain Interference subscale of the Brief Pain Inventory - Short Form (BPI-SF). The score is calculated as the mean of 7 items (each rated 0-10) and reported on a 0-100 scale

次要结局

  • Pain intensity at 7 days, measured by the BPI SF intensity score.(7 days)
  • Total amount of opioids consumed(7 days and 3 months)
  • Number of pain-free days after the emergency department visit(7 days)
  • Number of days off work(7 days and 3 months.)
  • Functional disability(3 months)
  • Patient satisfaction and quality of life(3 months)
  • Number of X-rays, CT scans, and MRI scans of the spine performed(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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