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临床试验/NCT04883216
NCT04883216已完成不适用

Investigation of the Characteristics of Chronic Pain Developing After COVID-19 in Patients With COVID-19

Istanbul University1 个研究点 分布在 1 个国家目标入组 776 人开始时间: 2021年3月24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
776
试验地点
1
主要终点
Self-Leeds Assessment of Neuropathic Symptoms & Signs (S-LANSS) Pain Score

研究概览

简要总结

Data on pain after COVID-19 were generally collected from hospitalized patients and only include information on acute pain conditions. However, the characteristics of the chronic pain experienced after COVID-19 are unknown. For this reason, the treatment and recommendations for patients who present with chronic pain after COVID-19 are not clear. Our goal is to determine the characteristics and risk factors of chronic pain developing in COVID-19 patients and to create specific treatment recommendations for these patient groups with further studies.

详细描述

Data on pain developing after COVID-19 were generally collected from hospitalized patients and only include information on acute pain conditions seen after the ilness. It is noteworthy that headache and musculoskeletal pain were seen common in first few weeks. However, the characteristics (mechanical, inflammatory, central sensitization, anxiety-related, etc.) of the chronic pain experienced are unknown. For this reason, the treatment and recommendations for patients who present with chronic pain after COVID-19 are not clear. Our goal is to determine the characteristics and risk factors of chronic pain developing in COVID-19 patients and to create specific treatment recommendations for these patient groups with further studies.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

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

  • Being over the age of 18
  • SARS-CoV-2 infection demonstrated with the PCR test (testing date irrelevant)
  • Pain developed or increased after having COVID-19

排除标准

  • Mental retardation or mental status not eligible to answer the questionnaires

结局指标

主要结局

Self-Leeds Assessment of Neuropathic Symptoms & Signs (S-LANSS) Pain Score

时间窗: up to 1 year

The S-LANSS aims to identify pain of predominantly neuropathic origin, as distinct from nociceptive pain, without the need for clinical examination.

The Hospital Anxiety and Depression Scale (HADS) Score

时间窗: up to 1 year

The Hospital Anxiety and Depression Scale (HADS) is a self-assessment questionnaire that has been found to be a reliable instrument for detecting states of anxiety and depression in the setting of hospital outpatient clinic. The HADS questionnaire has seven items each for depression and anxiety subscales.

Central Sensitization Inventory (CSI)

时间窗: up to 1 year

The Central Sensitisation Inventory (CSI) is a self-report outcome measure designed to identify patients who have symptoms that may be related to central sensitisation (CS) or central sensitivity syndromes (CSS) such as fibromyalgia, neck injury, temporomandibular joint disorder or migraine/tension headaches. CSI includes 25 questions related to common CSS symptoms.

Visual Analog Scale (VAS) for Pain

时间窗: up to 1 year

The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain."

Self-report Demographic Questionnaire

时间窗: up to 1 year

A questionnaire made by the researchers to understand the demographic characteristics of the patients included.

次要结局

未报告次要终点

研究者

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

Mert Zure

Medical Doctor

Istanbul University

研究点 (1)

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