Skip to main content
OpenTrials
Completed

NCT Number: NCT07427433

Amygdala Insula Retraining in the Management of Multiple Sclerosis Symptoms

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?

Completed

Looking for future studies?

Notify Me

Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Luther College Department of Psychology

Decorah, Iowa, 52101, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Confirmed multiple sclerosis diagnosis

Exclusion criteria

  • Previous experience with brain retaining programs

Treatment and study plan

Amygdala insula retraining

Behavioral

Mind body brain retraining intervention

lifestyle program

Behavioral

Mind body lifestyle intervention

Primary outcomes

  1. Fatigue Severity Scale

    Time frame: Baseline (Week 0) to post-intervention (Week 12)

Secondary outcomes

  1. PROMIS Pain Interference 8a

    Time frame: Baseline (Week 0) to post-intervention (Week 12)

  2. EQ-5D (quality of life)

    Time frame: Baseline (Week 0) to post-intervention (Week 12)

  3. GAD-7 (anxiety)

    Time frame: Baseline (Week 0) to post-intervention (Week 12)

  4. PHQ-9 (depression, with suicidality item excluded)

    Time frame: Baseline (Week 0) to post-intervention (Week 12)

  5. MSQ-Revised (exploratory)

    Time frame: Baseline (Week 0) to post-intervention (Week 12)

Sponsors and collaborators

Lead sponsor

Chronic Conditions Research Fund

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Feb 23, 2026
Registry last updated
Feb 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.