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Brain Connectivity and Perceptive Surfaces in Chronic Low Back Pain (SUPER-RMNf)

2026年7月31日 更新者:Teresa Paolucci、G. d'Annunzio University

Lombalgia Cronica Aspecifica e Superfici Percettive: Rappresentazione Corticale Del Tronco Nella Risposta al Trattamento Riabilitativo - Studio Quasi-sperimentale Non Randomizzato

Rationale:

Chronic Low Back Pain (CLBP) is often associated with "cortical reorganization," where the brain's map of the back becomes less precise. This phenomenon contributes to the persistence of pain and reduced body awareness. While traditional rehabilitation focuses on the physical structure of the spine, neurocognitive approaches use "perceptive surfaces" to provide specific tactile and proprioceptive feedback, aiming to "retrain" the brain's representation of the trunk.

Objective and Hypothesis:

The primary goal of this study is to investigate how the brain responds to stimulation from these perceptive surfaces in patients with CLBP compared to healthy individuals. The investigators hypothesize that using these surfaces will lead to immediate changes in functional brain connectivity, particularly in areas responsible for body awareness and pain processing (somatosensory and salience networks).

Study Procedures:

The study will involve 20 patients with chronic non-specific low back pain and 20 healthy volunteers. All participants will undergo a Functional Magnetic Resonance Imaging (fMRI) session. During the scan, participants will be placed on a specialized perceptive surface. Brain activity and connectivity will be measured at rest and during specific tactile stimulation. Additionally, advanced imaging techniques (SANDI model) will be used to look at the microscopic structure of brain cells (neurons).

Clinical Impact:

By comparing the two groups, the study aims to identify specific "brain signatures" of recovery. This could help clinical professionals understand if perceptive surfaces can effectively restore cortical maps, leading to better personalized rehabilitation strategies for chronic pain.

研究概览

地位

尚未招聘

研究类型

介入性

注册 (估计的)

40

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Chieti (CH)
      • Chieti、Chieti (CH)、意大利、66100
        • ITAB - Istituto di Tecnologie Avanzate Biomediche - Università degli Studi "G. d'Annunzio"
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

是的

描述

Inclusion Criteria:

  • Aged between 18 and 45 years
  • Right-handed dominance
  • Good general health condition
  • Ability to provide written informed consent.

For the patient group:

- Clinical diagnosis of non-specific chronic low back pain with a duration of more than 3 months

For the control group:

- Healthy volunteers without a history of chronic pain

Exclusion Criteria:

  • Contraindications to 3T Magnetic Resonance Imaging, such as pacemakers or non-compatible metallic implants
  • Pregnancy or breastfeeding
  • Presence of significant neurological or psychiatric pathologies
  • Current use of psychoactive medications.
  • Sensory or motor disorders of the lower limbs that prevent interaction with the perceptive surface.
  • Unstable or acute clinical conditions.
  • Inability to remain still during the MRI scanning procedure

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:CLBP Patients

This arm includes 20 participants with a clinical diagnosis of non-specific chronic low back pain (duration > 3 months).

Participants undergo a clinical and functional evaluation through validated scales (VAS, RMDQ, MPQ, Waddell Index, Zung SAS/SDS, BAQ).

The experimental procedure consists of a 3T MRI session including two resting-state fMRI blocks: one in a neutral condition and one while interacting with a "perceptive surface" (postural mat with sensory cones).

Advanced microstructural imaging (SANDI model) is also performed.

The intervention consists of a postural mat equipped with sensory cones of varying elastic memory and elasticity.

This tool is used as a neurocognitive rehabilitation device designed to restore body perception and postural control.

The device is passive, non-magnetic, and made of MRI-compatible latex (inert material).

During the fMRI session, the surface is positioned so that the participant, while lying in the scanner, perceives specific plantar or trunk tactile and proprioceptive stimuli.

有源比较器:Healthy Controls

This arm includes 20 healthy volunteers, aged 18-45, without history of chronic pain.

Participants undergo the same 3T MRI protocol as the clinical group (neutral vs. perceptive surface conditions) to provide a baseline for "normal" cortical representation and connectivity.

Clinical evaluations for this group are limited to demographic data and the Visual Analogue Scale (VAS) for pain/discomfort monitoring during the scan.

The intervention consists of a postural mat equipped with sensory cones of varying elastic memory and elasticity.

This tool is used as a neurocognitive rehabilitation device designed to restore body perception and postural control.

The device is passive, non-magnetic, and made of MRI-compatible latex (inert material).

During the fMRI session, the surface is positioned so that the participant, while lying in the scanner, perceives specific plantar or trunk tactile and proprioceptive stimuli.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Functional Connectivity Changes in Somatosensory and Salience Networks
大体时间:Periprocedural
Periprocedural

次要结果测量

结果测量
措施说明
大体时间
Neuronal Microstructure Mapping (SANDI model)
大体时间:Periprocedural
Periprocedural
Acute Pain Perception (Visual Analogue Scale)
大体时间:Day 1
Minimum Value: 0 Maximum Value: 10 Higher scores mean a worse outcome
Day 1
Functional Disability in CLBP Patients (Roland Morris Disability Questionnaire)
大体时间:Day 1
Minimum Value: 0 Maximum Value: 24 Higher scores mean a worse outcome
Day 1

其他结果措施

结果测量
大体时间
Brainstem Connectivity (PAG)
大体时间:Periprocedural
Periprocedural

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2026年12月1日

研究完成 (估计的)

2027年3月1日

研究注册日期

首次提交

2026年3月11日

首先提交符合 QC 标准的

2026年4月30日

首次发布 (实际的)

2026年5月5日

研究记录更新

最后更新发布 (实际的)

2026年8月4日

上次提交的符合 QC 标准的更新

2026年7月31日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • SUPER-RMNf
  • 447 (其他标识符:Comitato Etico Regione Abruzzo (Submission ID))

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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