# Stroke Investigation Group in North and Central London (SIGNAL): cohort profile of a prospective large-scale comprehensive stroke registry

**Authors:** Hatice Ozkan, Gareth Ambler, Philip S Nash, Simone Browning, Raafiah Mussa, Alex Leff, Hans R Jäger, Parashkev Nachev, Richard Perry, Edgar Chan, Robert Simister, David J Werring

PMC · DOI: 10.1136/bmjopen-2025-110772 · BMJ Open · 2026-01-30

## TL;DR

The SIGNAL registry is a large-scale stroke study tracking patients in London to understand stroke outcomes and improve care.

## Contribution

SIGNAL is a comprehensive stroke registry collecting detailed demographic, imaging, and long-term follow-up data from a diverse population.

## Key findings

- The registry includes 3931 stroke patients with detailed baseline and 6-month follow-up data.
- Most patients had moderate stroke severity and disability at discharge, with significant non-motor outcomes like fatigue and sleep issues.
- The registry plans to analyze stroke mechanisms and long-term outcomes over ~10 years.

## Abstract

Large-scale stroke registries can provide critical insights into disease mechanisms, progression and healthcare needs, informing prevention and care. However, few collect detailed demographic, brain imaging, and comprehensive long-term follow-up data. To address this, we established the prospective Stroke Investigation Group in North And central London (SIGNAL) registry in 2017.

The SIGNAL registry included 3931 adults aged ≥18 years with confirmed acute stroke (cerebral ischaemia or intracerebral haemorrhage (ICH)) admitted to the University College London Hospital hyperacute stroke unit between January 2017 and 2020, drawn from an ethnically diverse North and Central London population (~1.6 million). Baseline data included demographic, clinical, brain imaging and next-of-kin information. Six month follow-up included measures of functional status and non-motor outcomes (anxiety, depression, fatigue, sleep, pain, language, continence, social participation, cognition) via face-to-face, telephone or postal follow-up methods.

The mean age of individuals included in the SIGNAL registry was 72.1 years, and 1806 (45.9%) were female. The ethnic distribution comprised 2365 (60%) white, 649 (16.5%) black and 511 (13%) Asian. Stroke diagnoses included 3371 (85.8%) with cerebral ischaemia and 560 (14.2%) with ICH. On admission, 2240 individuals (57.0%) had a National Institutes of Health Stroke Scale score >4, indicating moderate stroke severity. At hospital discharge, the median functional outcome, measured by the modified Rankin Scale, was 3 (IQR 1–4), indicating moderate disability. At 6 months, functional outcomes measured with mRS were available for 3755 individuals (95.6%) with a median score of 1 (IQR=0–3) and non-motor outcomes were available for 3080 individuals (92.3%). The most prevalent adverse non-motor outcomes were fatigue 1756 (57%), reduced social participation 1694 (55%) and sleep disturbance 1663 (54%).

Further analyses of SIGNAL registry data will investigating associations between stroke mechanisms, subtypes and neuroimaging features and 6-month functional status, non-motor outcomes and cognitive impairment. Longer term follow-up of survivors for ~10 years is also planned.

## Linked entities

- **Diseases:** stroke (MONDO:0005098)

## Full-text entities

- **Diseases:** heart failure (MESH:D006333), cognitive impairment (MESH:D003072), death (MESH:D003643), cardiovascular disease (MESH:D002318), sleep disturbance (MESH:D012893), limb impairment (MESH:D001259), Hospital (MESH:D003428), constipation (MESH:D003248), atrial fibrillation (MESH:D001281), memory and (MESH:D008569), diabetes mellitus (MESH:D003920), based (MESH:D019292), Depression (MESH:D003866), COVID-19 (MESH:D000086382), communication problems (MESH:D003147), Anxiety (MESH:D001007), acute cerebral ischaemia (MESH:D000208), mood problems (MESH:D019964), pain (MESH:D010146), TIA (MESH:D002546), intracranial vascular stenosis or occlusion (MESH:D008641), infarcts (MESH:D007238), cerebral dysfunction (MESH:D002547), bladder dysfunction (MESH:D001745), reduced (MESH:D001523), Ischaemic stroke (MESH:D002544), hypertension (MESH:D006973), frailty (MESH:D000073496), cerebral ischaemia (MESH:D002545), Acute Stroke (MESH:D020521), ICH (MESH:D002543), small vessel disease (MESH:D059345), SAH (MESH:D013345), bowel dysfunction (MESH:D015212), problems (MESH:D019973), Aphasia (MESH:D001037), white matter hyperintensities (MESH:D056784), fatigue (MESH:D005221), NCL (MESH:C563785)
- **Chemicals:** Org 10 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12863321/full.md

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Source: https://tomesphere.com/paper/PMC12863321