Enhanced reviews of psychological changes after stroke

Not Applicable

• Conditions: Stroke; Circulatory System

• Registration Number: ISRCTN16018388
• Lead Sponsor: niversity of Oxford

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-07-26
• Last Update Posted: 5 August 2024
• Study Completion: 2027-04-30

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 170

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 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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Study 1: ENRICH review acceptability measured by a custom survey and qualitative data within approximately 1 week of receiving one ENRICH review<br><br>Study 2: Feasibility measured by descriptive statistics on recruitment, attendance, and completion of study measures over the course of the study<br>

Secondary Outcome Measures

Name	Time	Method
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