Stroke Circulatory System
Conditions
Interventions
Current interventions as of 30/12/2025:
Study 1: participants will receive one ENRICH review covering assessment, psychoeducation, and self-management of psychological changes after stroke. Consenting
Sponsors
University of Oxford
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: STUDY 1: Healthcare professionals: 1. Currently conducting ENRICH reviews of stroke survivors within Oxford University Hospital (OUH) Early Supported Discharge (ESD) service 2. Able and willing to give informed consent to participate in the study Stroke patients: 1. Confirmed clinical diagnosis of stroke by medical team 2. Aged 18 years or older 3. Ability to concentrate for 10 minutes, as judged by the clinical team 4. Able and willing to give informed consent to participate in the study, OR 5. Favourable consultee advice for adults lacking the capacity to consent Family members/carers: 1. Aged 18 years or older 2. Cohabiting with stroke survivor 3. Able and willing to give informed consent to participate in the study STUDY 2: NHS sites: 1. Existing early supported discharge (ESD) stroke service within NHS England 2. Existing 6-month reviews offered to all stroke patients within the service 3. Capacity for research activity within the clinical team (i.e., capacity for recruitment and to conduct enhanced reviews) Healthcare professionals: 1. Currently working within eligible stroke pathway NHS sites 2. Currently deliver stroke reviews within eligible stroke pathway NHS sites 3. Are able and willing to provide informed consent Stroke patients: 1. Aged 18 years or older 2. Within 4 weeks of confirmed clinical diagnosis of stroke (first-ever or recurrent) 3. Ability to concentrate for 10 minutes, as judged by the clinical team 4. Sufficient English fluency 5. Able and willing to provide informed consent, OR 6. Favourable consultee advice for adults lacking the capacity to consent Family members/carers: 1. Aged 18 years or older 2. Cohabiting with stroke survivor 3. Able and willing to provide informed consent
Exclusion criteria
Exclusion criteria: Exclusion will be based on not meeting the inclusion criteria above, as well as the below for Study 1 and Study 2: Family members/carers: 1. They are a paid or professional carer
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Study 1: ENRICH review acceptability measured by a custom survey and qualitative data within approximately 1 week of receiving one ENRICH review Study 2: Feasibility measured by descriptive statistics on recruitment, attendance, and completion of study measures over the course of the study | — |
Secondary
| Measure | Time frame |
|---|---|
| Study 2: Detailed quality of life measures at 6 months post-stroke as measured by the World Health Organisation-Quality of Life scale and the Quality of Life after Brain Injury Scale | — |
Countries
England, United Kingdom
Contacts
Public ContactNele;Andrea Demeyere;Kusec
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Outcome results
None listed