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临床试验/NCT07427433
NCT07427433已完成不适用

Amygdala Insula Retraining in the Management of Multiple Sclerosis Symptoms

Chronic Conditions Research Fund1 个研究点 分布在 1 个国家目标入组 132 人开始时间: 2024年9月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
132
试验地点
1
主要终点
Fatigue Severity Scale

研究概览

简要总结

The goal of this study is to compare a lifestyle intervention and a mind-body intervention against a wait-list control in individuals with multiple sclerosis experiencing persistent symptoms.

Our research questions include:

Are lifestyle and mind-body interventions additive to usual care in MS?

Can these interventions improve MS symptoms and overall quality of life?

详细描述

Multiple sclerosis (MS) is a chronic, immune-mediated neurological condition characterized by inflammation and neurodegeneration within the central nervous system. Despite advances in disease-modifying therapies, many individuals with MS continue to experience persistent and disabling symptoms, including fatigue, cognitive dysfunction, pain, mood disturbance, autonomic dysregulation, sleep disruption, and reduced quality of life. These symptoms often fluctuate and may persist independent of inflammatory disease activity, underscoring the need for adjunctive, non-pharmacologic interventions that target symptom burden and functional outcomes.

This study evaluates two distinct educational interventions designed to support symptom management in individuals with MS: a comprehensive lifestyle education program and a neuroplasticity-based brain retraining program known as Amygdala and Insula Retraining (AIR). Lifestyle-focused interventions targeting stress management, nutrition, sleep, physical activity, and environmental exposures have demonstrated benefits across chronic illness populations and are increasingly recognized as important components of comprehensive MS care. In parallel, growing evidence supports the role of mind-body approaches in modulating autonomic nervous system function, stress, and measurable effects on fatigue, mood, pain, quality of life, and heart rate variability.

AIR is based on the principle that chronic illness and inflammatory stressors may sensitize neural circuits involved in threat detection and interoception, particularly the amygdala and insula, leading to persistent hypervigilance and maladaptive autonomic signaling. In MS, this heightened neural reactivity may contribute to symptom amplification such as increased fatigue, dysautonomia, and reduced stress resilience. AIR aims to de-sensitize these neural pathways through structured neuroplasticity-based cognitive and mindfulness practices, with the goal of interrupting maladaptive feedback loops and supporting improved autonomic and emotional regulation.

In this randomized pilot study, individuals with MS will be assigned to one of three groups: a lifestyle education program, the AIR program, or a wait-list control group. By comparing changes in validated symptom and quality-of-life measures across groups over time, this study aims to generate preliminary data on the feasibility and potential symptom-modifying effects of both interventions, informing the design of larger, controlled trials.

研究设计

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

入排标准

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

入选标准

  • Confirmed multiple sclerosis diagnosis

排除标准

  • Previous experience with brain retaining programs

研究组 & 干预措施

Amygdala insula retraining

Experimental

Mind body amygdala insula retraining intervention delivered virtually + usual care

干预措施: Amygdala insula retraining (Behavioral)

Lifestyle program

Experimental

Mind body lifestyle intervention

干预措施: Lifestyle program (Behavioral)

Control

No Intervention

结局指标

主要结局

Fatigue Severity Scale

时间窗: Baseline (Week 0) to post-intervention (Week 12)

次要结局

  • GAD-7 (anxiety)(Baseline (Week 0) to post-intervention (Week 12))
  • PHQ-9 (depression, with suicidality item excluded)(Baseline (Week 0) to post-intervention (Week 12))
  • MSQ-Revised (exploratory)(Baseline (Week 0) to post-intervention (Week 12))
  • PROMIS Pain Interference 8a(Baseline (Week 0) to post-intervention (Week 12))
  • EQ-5D (quality of life)(Baseline (Week 0) to post-intervention (Week 12))

研究者

发起方
Chronic Conditions Research Fund
申办方类型
Other
责任方
Sponsor

研究点 (1)

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