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临床试验/NCT05186259
NCT05186259已完成不适用

Modulating Mechanisms in Patients With Chronic Subjective Tinnitus and/or Chronic Pain

University Ghent2 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2021年12月21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
135
试验地点
2
主要终点
Between-group differences in mechanical pain sensitivity by means of pressure detection and pain thresholds (expressed in kgf)

研究概览

简要总结

This is a cross-sectional investigation into modulating mechanisms in patients with chronic subjective tinnitus, which will compare 4 patient groups namely chronic tinnitus with chronic pain, chronic tinnitus without chronic pain, chronic pain without tinnitus and healthy controls.

详细描述

The first aim is to investigate differences in pain-related factors, psychological factors, lifestyle factors and tinnitus-related factors in patients with chronic subjective tinnitus and the comparison with patients suffering from both chronic subjective tinnitus and chronic musculoskeletal pain, chronic musculoskeletal pain only and healthy controls. The primary outcome measures will be pain-related factors and correlations will also be calculated between pain-related factors on the one hand and psychological factors, lifestyle factors and tinnitus-related factors on the other hand.

A second aim is to assess contributing factors to tinnitus severity (measured by the Tinnitus Functional Index) in patients with tinnitus with or without chronic pain. Contributing factors will include pain-related factors, psychological factors, lifestyle factors, and tinnitus-related factors, audiological factors, cognitive factors.

  • Pain-related factors include:
  1. Self-perceived symptoms of central sensitization by means of the Central Sensitization Inventory: The Central Sensitization Inventory is a self-report questionnaire that assesses clinical symptoms indicative for central sensitization.
  2. Experimental measures of central sensitization: Quantitative Sensory Testing Quantitative Sensory Testing (QST) is a psychophysiological assessment of sensory pathways including mechanicaldetection and pain thresholds, cutaneous heat detection and pain thresholds, and endogenous pain facilitation and inhibition.
  3. Self-reported pain processing by means of the Pain Catastrophizing Scale
  4. Self-reported neck pain related disability by means of the Neck Disability Index
  • Psychological factors include:

Self-reported stress, anxiety and depression (Depression, Anxiety and Stress Scale_21 and Beck Depression Inventory), resilience (Connor Davidson Resilience Scale), personality (Big Five Index)

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

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

入选标准

  • Chronic subjective tinnitus patients without chronic pain:
  • Aged between 18-65 years
  • Chronic subjective tinnitus (> 3 months during most of the days (4 or more)and for more than 5 minutes/day)
  • Speaking and understanding Dutch fluently
  • Chronic subjective tinnitus patients with chronic pain:
  • Aged between 18-65 years
  • Chronic subjective tinnitus (> 3 months during most of the days (4 or more)and for more than 5 minutes/day)
  • Speaking and understanding Dutch fluently
  • Persistent musculoskeletal pain lasting more than 3 months
  • Mean pain intensity of more than 3 of 10 on a numeric pain rating scale during the preceding month (the cutoff for clinically relevant pain)
  • Chronic ideopathic neck pain:
  • Aged between 18-65 years
  • Persistent neck pain lasting more than 3 months
  • Mean pain intensity of more than 3 of 10 on a numeric pain rating scale during the preceding month (the cutoff for clinically relevant pain)
  • Healthy controls:
  • Aged between 18-65 years

排除标准

  • Chronic subjective tinnitus with/without chronic pain:
  • Objective tinnitus
  • Subjective tinnitus caused by clear causes such as tumor, trauma, vascular dysfunction, neurological disorder, pulsatile tinnitus
  • Vertigo (Menière's disease, BPPV,...)
  • Progressive middle ear pathology
  • Intracranial pathologies
  • Subjects with prior otologic surgery (for example stapedotomy), active outer or middle ear pathology
  • History of head, neck or shoulder trauma or surgery (< 5 years, or remaining complaints)
  • A history of whiplash trauma
  • Major depression or psychiatric illness (diagnosed by a psychiatrist and being in medicamental or psychiatric treatment)
  • Life threatening, metabolic, cardiovascular, neurologic, systemic diseases
  • Diagnosis of fibromyalgia/chronic fatigue syndrome
  • Pregnancy or given birth in the preceding year
  • Dyslexia, dyscalculia, AD(H)D, language/communication disorder
  • Chronic subjective tinnitus without chronic pain (additional exclusion criteria):
  • No history of chronic pain
  • No pain condition in the last 6 months for which treatment was sought
  • No pain in any region > 2/10 on the testing day
  • Chronic ideopathic neck pain:
  • Ever experienced whiplash trauma or other form of trauma to the head, neck, or upper quadrant
  • Specific causes of neck pain, such as cervical hernias with clinical symptoms
  • Major depression or psychiatric illness (diagnosed by a psychiatrist and being in medicamental or psychiatric treatment)
  • Life threatening, metabolic, cardiovascular, neurologic, systemic diseases
  • Diagnosis of fibromyalgia/chronic fatigue syndrome
  • A history of neck, head or shoulder girdle surgery
  • A history of whiplash trauma
  • Pregnancy or given birth in the preceding year
  • Diagnosis of any TMD, according to the Research Diagnostic Criteria for TMD (RDC/TMD); or concomitant diagnosis of primary headache
  • Healthy controls:
  • Any form of tinnitus and/or hyperacusis
  • Experiencing any type of pain during at least 8 consecutive days with an NRS higher than 2/10 in the preceding year
  • Reported pain on the day of testing (VAS higher than 2/10)
  • Vertigo (Menière's disease, BPPV,...)
  • History of head, neck or shoulder trauma or surgery (< 5 years, or remaining complaints)
  • Wearing a hearing aid device, implant, noise generators or receiving neuromodulation therapy
  • Intracranial pathologies
  • History of head, neck or shoulder trauma or surgery (< 5 years, currently no complaints)
  • Major depression or psychiatric illness (diagnosed by a psychiatrist and being in medicamental or psychiatric treatment)
  • Life threatening, metabolic, cardiovascular, neurologic, systemic diseases
  • A history of whiplash trauma
  • Diagnosis of fibromyalgia/chronic fatigue syndrome
  • Pregnancy or given birth in the preceding year

结局指标

主要结局

Between-group differences in mechanical pain sensitivity by means of pressure detection and pain thresholds (expressed in kgf)

时间窗: At baseline

Pain sensitivity will be assessed by a mechanical stimulus, which is given by the tester with a digital pressure algometer (FDX; Wagner Instruments) at a rate of 1 kg pressure rise per second. The participant is asked to say 'yes' if the point was reached when the pressure stimulus causes a sensation of pain (detection threshold), the tester continues giving pressure until the patient says 'yes' for a second time indicating the feeling of pain reached a 6/10 of the NRS (pain threshold). T Two consecutive measurements with a break of 30 seconds are performed. This protocol is performed at 5 standardized body locations, being: C5-C cervical joint, N. Trigeminus, M. Masseter, M. Extensor carpi radialis longus, M. Tibialis Anterior

次要结局

  • Tinnitus analysis(At baseline)
  • Between-group differences in self-reported signs of central sensitization by means of the Dutch version of the Central Sensitization Inventory (questionnaire)(At baseline)
  • Audiometric assessments(At baseline)
  • Between-group differences in heat pain sensitivity by means of heat detection and pain thresholds (expressed in °)(At baseline)
  • Between-group differences in endogenous pain facilitation by means of a temporal summation protocol (expressed in pain scores (numeric rating scales, NRS)(At baseline)
  • Between-group differences in endogenous pain inhibition by means of conditioned pain modulation protocol (expressed in kgf and °)(At baseline)
  • Between-group differences in self-reported quality of life(At baseline)
  • Between-group differences in self-reported psychological factors(At baseline)
  • Between-group differences in self-reported lifestyle factors(At baseline)
  • Between-group differences in self-reported neck pain related measures(At baseline)
  • Between-group differences in self-reported tinnitus related measures(At baseline)
  • Cognitive functioning(At baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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