跳至主要内容
临床试验/CTRI/2025/11/097886
CTRI/2025/11/097886尚未招募不适用

Efficacy of Self managed Psychoeducation based Pain management program in Reducing Pain Intensity in Patients with Chronic Low Back Pain

Senior Research Fellowship (SRF) from the University Grants Commission (UGC)1 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31日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
Visual analogue scale (VAS)

研究概览

简要总结

Chronic low back pain can substantially reduce a patient’s quality of life, affecting physical functioning, emotional well-being, and the capacity to engage in occupational and social activities. Individuals experiencing chronic low back pain often endure significant distress in their daily lives.. Additionally, patients from middle to low socioeconomic backgrounds may face challenges in attending regular sessions designed to manage their chronic low back pain, due to factors such as travel costs, limited awareness, and poor accessibility. Multiple treatment options exist for such patients that may be invasive (surgical) or non-invasive (conservative) in nature.  The program offers a cost-effective, non-invasive, and accessible treatment option for these patients that incorporates psychotherapy and psychoeducation techniques. Notably, there is a paucity of research on Indian patients with chronic low back pain. The subjective pain experience of the patient may be influenced by social, psychological, and cultural factors, necessitating more studies within the Indian context

研究设计

研究类型
Interventional
分配方式
Na
盲法
Participant Blinded

入排标准

年龄范围
13.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Patients suffering from low back pain for more than 12 weeks ii.
  • Cooperative patients.

排除标准

  • Participants with existing pregnancy ii.
  • Participants with a past history of psychiatric disorders (such as anxiety, depression, PTSD) iii.
  • Participants with a history of spinal surgery.

结局指标

主要结局

Visual analogue scale (VAS)

时间窗: Upon admission (T1) | 3 months (T2) | 6 months (T3)

次要结局

  • Generalized anxiety scale 7 (GAD 7)(Upon admission (T1))
  • Roland-Morris disability questionnaire (RMDQ)(Upon admission (T1))
  • Patient Health Questionnaire 9(Upon admission (T1))
  • Pain catastrophizing scale (PCS)(Upon admission (T1))

研究者

发起方
Senior Research Fellowship (SRF) from the University Grants Commission (UGC)
申办方类型
Government funding agency
责任方
Principal Investigator
主要研究者

Nityanand Pandey

Banaras Hindu University

研究点 (1)

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