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临床试验/NCT05857761
NCT05857761进行中(未招募)不适用

Post-traumatic Headache: Phenotyping and Exploring Pathophysiological Insights and Novel Treatment Strategies

University of Aarhus2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2023年8月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
62
试验地点
2
主要终点
Change in the number of headache days of moderate to severe intensity

研究概览

简要总结

The overall aim of the study is to advance the knowledge on the characterization and underlying pathophysiological mechanisms of persistent post-traumatic headache (PTH) with a direct impact on the ability to diagnose and manage PTH effectively. The investigators also aim to evaluate the efficacy of repetitive transcranial magnetic stimulation (rTMS), a novel intervention on PTH.

详细描述

Post-traumatic headache (PTH) is one of the most common and persistent symptoms following mild traumatic brain injury (mTBI), with an estimation of 18-22% developing persistent (> 3 months) PTH. PTH is highly disabling. Unfortunately, its typical characteristics and pathophysiology are poorly understood leading to its complicated and diverse management.

There is no agreement on the clinical presentation of PTH.This is largely due to the scarcity of longitudinal prospective data on large cohorts of PTH. Describing headache phenotypes longitudinally might improve disease characterization, facilitate better classification and provide evidence based-criteria of diagnosing PTH. Furthermore, exploring biomarkers associated with mTBI may provide new knowledge on the poorly understood pathophysiology of post commotional symptoms (PCS) and PTH. Additionally, there are indications of somatosensory disturbances and impaired endogenous analgesic systems in PTH patients. Assessment of somatosensory signs and symptoms in relation to pain complaints and functioning of endogenous analgesic system may also aid in better understanding of pain mechanisms in these patients. Functioning of endogenous analgesic system can be assessed using conditioned pain modulation (CPM) paradigms. Further, a curious observation in concussion patients with face and/or head pain is that they perceive painful/affected area (head and/or face region) as "swollen" or "different" without any clinical signs or obvious physical differences. Hence, such "illusions" represent body image distortions or perceptual distortion (PD) of the head or face region, and may contribute to the chronification of pain. PD can significantly affect psychosocial well-being of patients as the face/head region is a key feature of one´s identity. Unfortunately, such a distressing phenomenon has not been investigated before in these patients. Currently, no strong evidence-based treatment guidelines for PTH exist. Neuromodulation using repetitive transcranial magnetic stimulation (rTMS) targeting involved brain regions and functional networks has recently been employed to treat several chronic pain conditions including migraine. Thus, rTMS could offer an optimal new treatment strategy for PTH, as there is an evidence of brain network dysfunction in these patients.

The overall aim is to advance the knowledge on the characterization and underlying pathophysiological mechanisms of persistent PTH. The aim is also to measure the prevalence of perceived size changes (PD) of head and/or face region in patients with mild traumatic brain injury and its association with pain/PTH and other post commotional symptoms (PCS). The investigators will also evaluate the efficacy of rTMS on PTH. Deep phenotyping of PTH will be performed. Blood samples from mTBI patients will be examined for the biomarkers of PCS and PTH and the association between the biomarkers and the symptom levels of PCS, in particular PTH frequency and intensity will be evaluated. Baseline biomarker levels in the blood samples from patients with mTBI will be compared to biomarker levels in blood samples from anonymous healthy age- and sex matched controls (blood donors) or published reference intervals from the litterature. Additionally, the association between somatosensory function including CPM and the PTH frequency and intensity will be examined. Further, the effect of rTMS on headache severity and frequency (primary outcome) and somatosensory function, PD and other PCS (secondary outcome) after 1 and 3 months of stimulation will be evaluated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

盲法说明

A computer will randomize participants to either participate in the active- or the sham group. At end of treatment participants will be asked to answer if they have received sham- or active treatment in order to assess the success of participant-blinding.

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • mTBI within the last 2 to 4 months according to the diagnostic criteria recommended by the WHO task force
  • age ≥ 18 years at the time of mTBI
  • Rivermead Post-Concussion Symptoms Questionnaire (RPQ) score ≥ 3 (moderate or severe problem) for subitem headache and a diagnosis of persistent PTH attributed to mTBI according to ICHD-
  • Additionally, for study 2 and 3, subjects have to be stable on preventative headache medication. However, subjects are permitted to take ''as needed'' (PRN) medications throughout the study with documentation in a daily headache diary.

排除标准

  • objective neurological findings and/or acute trauma CT scan indicating neurological disease or brain damage
  • previous mTBI within the last 2 years years leading to PCS lasting ≥ 3 months. Additionally, for study 2 and 3,
  • Pre-trauma headache frequency ≥ 10 days in average per month the last 3 months prior to mTBI.
  • past history of TMS therapy or TMS-related contraindications (pacemaker, epilepsy etc.).

研究组 & 干预措施

Active rTMS treatment

Active Comparator

Participants (n=31) will receive active rTMS treatment.

干预措施: Active repetitive transcranial magnetic stimulation (rTMS) (Device)

Sham group

Sham Comparator

participants (n=31) will receive sham rTMS.

干预措施: Sham repetitive transcranial magnetic stimulation (rTMS) (Device)

结局指标

主要结局

Change in the number of headache days of moderate to severe intensity

时间窗: Prior to intervention compared to 1 month after end of treatment.

Change in the number of headache days of moderate to severe intensity from baseline to 1-month post intervention based on a self-reported daily headache diary, a self-reported headache questionaire and Headache Impact test (HIT-6).

A comparison at baseline of the blood biomarker concentrations in the mTBI patients compared to healthy controls

时间窗: Prior to rTMS intervention

Differences in the blood biomarkers (such as neurofilament light chain, calcitonin gene related peptide, pituitary adenylate cyclase-activating polypeptide, cytokines, mRNA, microRNA and circular RNA) at baseline.

Characterization of PTH headache phenotypes using a self-constructed headache questionaire.

时间窗: 3 months after mTBI

Characterization of PTH headache phenotypes into e.g. migraine-like or tension-type like using a self-constructed headache questionnaire.

Changes in the concentration of biomarkers

时间窗: Prior to rTMS intervention, immediately after rTMS intervention and 1 month after end of treatment

Changes in the blood biomarkers (such as neurofilament light chain, calcitonin gene related peptide, pituitary adenylate cyclase-activating polypeptide, cytokines, mRNA, microRNA and circular RNA) and somatosensory function from baseline to immediately after the completion of intervention (rTMS) and 1 month post-rTMS. Associations between total symptomload (Total RPQ score) and blood biomarker concentrations will be investigated.

次要结局

  • Change in Psychological Distress(Prior to intervention compared to 1 and 3 months after end of treatment.)
  • Change in facial perception(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Change in self-reported efficacy of treatment(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Changes in sleep quality(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Changes in the somatosensory function.(prior to rTMS intervention, immediately after rTMS intervention and 1 month after end of treatment)
  • Characterization of PTH headache phenotypes using the Headache Impact Scale.(3 months after mTBI)
  • Changes in headache phenotype using a self-constructed headache questionaire.(3, 9 and 12 months after mTBI)
  • Changes in headache phenotype using the Headache Impact Scale .(3, 9 and 12 months after mTBI)
  • Change in how neck pain affects daily life(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Change in the number of headache days of moderate to severe intensity(Prior to intervention compared to 3 months after end of treatment.)
  • Change in severity of post-concussion symptoms covering physical, cognitive, and emotional symptoms.(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Change in self-reported impact on participation and autonomy(Prior to intervention compared to 1 and 3 months after end of treatment.)
  • Change in illness perception(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Change in Pain Catastrophizing(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Change in the use of medication, non-pharmacological treatment and management strategies.(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Change in health-related quality of life(Prior to intervention compared to 1 and 3 months after end of treatment)
  • Changes in headache impact measured on the Headache Impact Scale.(baseline, 1 months after end of treatment, 3 months after end of treatment)

研究者

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

Charlotte Nygaard

Medical Doctor, PhD student

Regionshospitalet Hammel Neurocenter

研究点 (2)

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