# Study protocol for a mixed methods convergent investigation of family domestic and sexual violence in multiple sclerosis and broader neurology in Australia

**Authors:** Cassie Nesbitt, Genevieve Rayner, Kristen Timmens, Christina Kazzi, Rubina Alpitsis, Emma Foster, Jason Ray, Joanne Crosby, Helmut Butzkueven, Anneke Van Der Walt, Vilija G. Jokubaitis, Yordanis Enríquez Canto, Yordanis Enríquez Canto, Yordanis Enríquez Canto

PMC · DOI: 10.1371/journal.pone.0344667 · PLOS One · 2026-03-13

## TL;DR

This study explores how family, domestic, and sexual violence affects people with multiple sclerosis and other neurological conditions in Australia, aiming to improve healthcare responses.

## Contribution

The study introduces a mixed-methods approach to investigate FDSV in neurology, adapting global frameworks like LIVES and MARAM for clinical practice.

## Key findings

- Estimates prevalence and forms of FDSV among people with MS.
- Identifies social, clinical, and contextual factors linked to FDSV in neurological populations.
- Documents current neurology practices for recognizing and responding to FDSV.

## Abstract

People with disabilities experience disproportionately high rates of family, domestic, and sexual violence (FDSV), yet recognition and response in neurological healthcare, including multiple sclerosis (MS), remain underexplored. The study is informed by evidence-based frameworks for healthcare responses to family, domestic, and sexual violence, including the World Health Organization’s Listen, Inquire, Validate, Enhance safety, Support access (LIVES) approach and Victoria, Australia’s Multi-Agency Risk Assessment and Management (MARAM) framework. These models share core principles of trauma-informed practice, structured risk assessment, and coordinated response, providing a foundation for investigating how such approaches can be applied and adapted within neurological care.

This study aims to estimate the prevalence and describe the forms of FDSV experienced by people with MS, identify associated social, clinical, and contextual factors, and document current neurology practices for recognising and responding to FDSV. Comparative qualitative analysis across MS, epilepsy, and headache will assess whether findings are condition-specific or shared across neurology to inform future strategies.

A convergent mixed-methods design will be applied across six study arms. Quantitative components include screening approximately 1,000 people with MS, registry linkage, and surveys with at least 100 participants assessing trauma exposure, wellbeing, and disability-related violence. Qualitative interviews with people with MS, epilepsy, and headache, and clinicians (n ≈ 64 total) will explore experiences, clinical practice, and barriers and enablers to implementing evidence-based frameworks. Data will be integrated through triangulation to identify convergent and divergent patterns.

Findings will provide foundational evidence on how MS and other neurological conditions intersect with experiences of FDSV, guiding trauma-informed training, policy, and practice across neurology.

Australian New Zealand Clinical Trials Registry (ANZCTR), ACTRN390279.

## Linked entities

- **Diseases:** multiple sclerosis (MONDO:0005301), epilepsy (MONDO:0005027)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** Depression (MESH:D003866), type 2 diabetes (MESH:D003924), obesity (MESH:D009765), ACE (OMIM:300909), epilepsy (MESH:D004827), Trauma (MESH:D014947), IPV (MESH:C563733), neurological conditions (MESH:D019636), headache (MESH:D006261), CIS (MESH:D059466), distress (MESH:D012128), FDSV (MESH:D050035), emotional or psychological abuse (MESH:D000067073), abuse (MESH:D019966), cardiovascular disease (MESH:D002318), physical (MESH:D059445), MS (MESH:D009103), somatic disorders (MESH:D013001), disabilities (MESH:D009069), vision or hearing impairments (MESH:D054062), chronic neurological conditions (MESH:D002908), conditions (MESH:D020763), neglect (MESH:D058069), physical and or sexual abuse (MESH:D000082002), inflammatory (MESH:D007249), head injury (MESH:D006259), Anxiety (MESH:D001007), family violence (MESH:D000073376), Fatigue (MESH:D005221), chronic pain (MESH:D059350), neurology (MESH:D009461), hypertension (MESH:D006973)
- **Chemicals:** PONE-D-25-65254R1 (-), Alcohol (MESH:D000438), DMT (MESH:D004130)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12987488/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987488/full.md

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Source: https://tomesphere.com/paper/PMC12987488