Skip to content

From risk to response: recognising and responding to family domestic and sexual violence in Multiple Sclerosis (MS) and broader neurology

From risk to response: recognising and responding to family domestic and sexual violence (FDSV) in Multiple Sclerosis and broader neurology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12625001257459
Enrollment
10
Registered
2025-11-12
Start date
2025-08-04
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study will look at experiences of family, domestic, and sexual violence in people with multiple sclerosis and other neurological conditions. Participants will complete one-time screening, surveys, and optional interviews about their experiences and care, with this information linked to medical records and the MSBase registry. Outcomes of multiple sclerosis will be followed for three years. The study aims to understand how violence affects health and wellbeing, whether it worsens MS through other illnesses and the psychological impact of trauma, and to improve how neurology recognises and responds to violence. Lessons from MS are expected to inform responses across the wider field of neurology.

Interventions

Family, domestic, and sexual violence exposure is assessed once at enrolment through structured screening and once via validated surveys post-enrolment. Retrospective MSBase and clinical data (EDSS, relapses, MRI, comorbidities, neuropsychology scores, medications) are collected at enrolment to capture prior disease course. Prospective MS outcomes are then recorded through routine MSBase and clinical follow-up every 3–12 months for 3 years. Qualitative interviews are conducted once per participa

Family, domestic, and sexual violence exposure is assessed once at enrolment through structured screening and once via validated surveys post-enrolment. Retrospective MSBase and clinical data (EDSS, relapses, MRI, comorbidities, neuropsychology scores, medications) are collected at enrolment to capture prior disease course. Prospective MS outcomes are then recorded through routine MSBase and clinical follow-up every 3–12 months for 3 years. Qualitative interviews are conducted once per participant. a) Condition/exposure The study observes people with Multiple Sclerosis (MS) and examines exposure to family, domestic, and sexual violence (FDSV). b) Observational data collected Data captured includes MS outcomes (EDSS, relapses, MRI), comorbidities, neuropsychology scores, medications, and prospectively recorded clinical data every 3–12 months. Retrospective data will also be collected from prior outpatient visits documented in the MSBase database. c) Procedures for participants Participants are not required to undertake any additional clinical procedures beyond their usual outpatient neurology visits. The study involves collation of routinely recorded clinical data supplemented by standardised surveys/questionnaires where relevant. d) Frequency and duration of observation Data is collected prospectively at routine visits every 3–12 months over a three-year period. Retrospective data will be extracted from existing medical records in MSBase and outpatient records prior to enrolment. Retrospective data Retrospective data includes MS outcomes (EDSS, relapses, MRI findings), comorbidities, neuropsychology scores, and medication history recorded at prior outpatient neurology visits. This information will be extracted from the MSBase database and site clinical records.

Sponsors

Monash University
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Multiple Sclerosis

Exclusion criteria

Unable to participate independently Recent lived experience of family violence and unsafe as per MARAM risk indicators Unstable mental illness Under influence of drugs and or alcohol Pregnant or breastfeeding Non medicare eligible

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026