跳至主要内容
临床试验/NCT07125781
NCT07125781已完成不适用

Prevalence of Central Sensitization and Nociplastic Pain in Individuals Diagnosed With Pes Planus: A Multicenter Cross-Sectional Study

Bozok University1 个研究点 分布在 1 个国家目标入组 214 人开始时间: 2024年11月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
214
试验地点
1
主要终点
Pain-DETECT questionnaire

研究概览

简要总结

Background:

Pes planus, commonly known as flatfoot, is a condition characterized by the collapse of the medial longitudinal arch of the foot. While some individuals remain asymptomatic, many experience foot or leg pain, walking difficulties, and functional limitations. In some cases, symptoms persist despite adequate conventional treatment. This suggests that central pain mechanisms, such as central sensitization and nociplastic pain, may contribute to ongoing symptoms. These mechanisms involve changes in the central nervous system that amplify pain perception and can occur even in the absence of active tissue damage. Understanding these mechanisms in pes planus may help guide more targeted and effective treatment strategies.

Purpose:

The aim of this multicenter cross-sectional study was to determine the prevalence of central sensitization and nociplastic pain in individuals with clinically diagnosed pes planus and to compare the findings with age- and sex-matched healthy controls.

Methods:

Between November 2024 and May 2025, a total of 107 patients with pes planus and 107 healthy controls were recruited from three medical centers. Participants completed validated Turkish versions of the Visual Analog Scale for pain intensity, the Foot Function Index for functional limitation, the Pain-DETECT questionnaire for nociplastic pain symptoms, the Central Sensitization Inventory for central sensitization, the Hospital Anxiety and Depression Scale for psychological distress, and the Short Form-12 for quality of life. Data were analyzed using comparative statistical tests and multiple linear regression models to identify factors associated with nociplastic pain and central sensitization in the pes planus group.

详细描述

Pes planus, also referred to as flatfoot, is a common musculoskeletal condition characterized by the flattening or collapse of the medial longitudinal arch of the foot. It affects a considerable portion of the adult population and may be associated with foot pain, functional impairment, and reduced quality of life. In many patients, pain symptoms persist despite adequate structural correction and conventional treatments such as footwear modifications, orthotic support, exercise, or anti-inflammatory medications. This persistence suggests that central mechanisms of pain processing may be involved.

Central sensitization is a phenomenon in which the central nervous system exhibits heightened responsiveness to sensory input, resulting in amplified pain perception even in the absence of ongoing tissue injury. Nociplastic pain is a relatively new classification describing pain arising from altered central nociceptive processing without clear evidence of tissue damage or nerve injury. Both mechanisms are increasingly recognized in chronic musculoskeletal disorders, yet they have been underexplored in individuals with pes planus.

This multicenter cross-sectional study was designed to investigate the prevalence of central sensitization and nociplastic pain in adults with clinically diagnosed pes planus and to compare these findings with healthy controls matched for age and sex. Participants were recruited from three medical centers between November 2024 and May 2025. Inclusion criteria required adults aged 18 to 65 years with lower extremity pain lasting at least six months and a diagnosis of pes planus confirmed by a physical medicine and rehabilitation specialist. Healthy controls had no history of foot or leg pain or relevant musculoskeletal disorders.

All participants completed standardized and validated assessment tools, including the Visual Analog Scale for pain intensity, the Foot Function Index for foot-related disability, the Pain-DETECT questionnaire for nociplastic pain features, the Central Sensitization Inventory for signs of central sensitization, the Hospital Anxiety and Depression Scale for psychological distress, and the Short Form-12 for quality of life. Demographic and clinical information was also recorded.

Statistical analyses compared results between the pes planus and control groups and examined correlations among pain severity, functional impairment, central sensitization, nociplastic pain, and psychological measures. Multiple linear regression models were used to identify independent predictors of nociplastic pain and central sensitization in the pes planus group.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age between 18 and 65 years.
  • •For pes planus group: clinically diagnosed pes planus confirmed by physical medicine and rehabilitation specialists, with persistent lower extremity pain for at least 6 months.
  • •For control group: age- and sex-matched healthy volunteers without current or past foot or leg pain.
  • •Willingness to complete all self-report questionnaires.
  • •Provided written and verbal informed consent.

排除标准

  • •History of diabetes mellitus, hypothyroidism, malignancy, vasculitis, neuropathies, or lumbar radiculopathy.
  • •History of lower limb surgery or trauma.
  • •Recent local injection or extracorporeal shockwave therapy.
  • •Any rheumatologic disease affecting pain perception (e.g., rheumatoid arthritis, ankylosing spondylitis).
  • •Severe psychiatric disorder or cognitive impairment interfering with questionnaire completion.

结局指标

主要结局

Pain-DETECT questionnaire

时间窗: Baseline

The Pain-DETECT questionnaire consists of 9 items with a total score range of 1-38. Scores ≤12 indicate that neuropathic or nociplastic pain components are unlikely, 13-18 indicate uncertainty, and ≥19 indicate probable nociplastic or neuropathic pain. The validated Turkish version, developed by Alkan et al. (2013), demonstrated a sensitivity of 90% and specificity of 67.5% for the ≤12 cutoff, with a negative predictive value of 87%.

Central Sensitization Inventory

时间窗: Baseline

The Central Sensitization Inventory contains 25 items scored 0-4 (0 = never, 4 = always). Total scores ≥40 indicate the presence of central sensitization, with severity categories as follows: 0-29 subclinical, 30-39 mild, 40-49 moderate, 50-59 severe, ≥60 very severe. The validated Turkish version, developed by Keleş et al. (2021), reported 81% sensitivity and 75% specificity for the ≥40 cutoff, with excellent internal consistency (Cronbach's alpha = 0.92) and test-retest reliability (intraclass correlation coefficient = 0.93).

次要结局

  • Hospital Anxiety and Depression Scale(Baseline)
  • Visual Analog Scale(Baseline)
  • Foot Function Index(Baseline)
  • Short Form-12 Health Survey (SF-12)(Baseline)

研究者

发起方
Bozok University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gulseren Demir Karakilic

Assistant Professor, Principal Investigator

Bozok University

研究点 (1)

Loading locations...

相似试验