Skip to content

Oxford Cognitive Screen (OCS)-care: a study for developing and evaluating a care pathway for cognitive problems after stroke

A randomised controlled pilot study for developing and evaluating a care pathway for cognitive problems after stroke (the OCS-care project)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN50857950
Enrollment
400
Registered
2014-03-27
Start date
2014-03-01
Completion date
Unknown
Last updated
2018-02-12

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

Conditions

Stroke Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

Standard care arm only (within 2 months of stroke): 1. MOCA. This is a 15min paper-and-pencil test currently used as a cognitive screening tool in dementia and as a short screen in acute stroke units

Sponsors

University of Oxford (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Stroke patients up to 90 years of age, plus their main carer Patients: 1. Having had a stroke 2. Sufficient concentration to take part in paper and pencil tests for 1 hour (judged by the multi-disciplinary team in the hospital) 3. Sufficient language comprehension to pass the first orienting tests in the OCS. Within 2 months of the stroke 4. Male or female adults up to 90 years of age 5. Willing and sufficiently able to give informed consent to take part in the study Carers: 1. Being the primary carer of stroke patient enrolled in the study 2. Willing and able to give informed consent;Inclusion criteria: Stroke patients up to 90 years of age, plus their main carer Patients: 1. Having had a stroke 2. Sufficient concentration to take part in paper and pencil tests for 1 hour (judged by the multi-disciplinary team in the hospital) 3. Sufficient language comprehension to pass the first orienting tests in the OCS. Within 2 months of the stroke 4. Male or female adults up to 90 years of age 5. Willing and sufficiently able to give informed consent to take part in the study Carers: 1. Being the primary carer of stroke patient enrolled in the study 2. Willing and able to give informed consent

Exclusion criteria

Exclusion criteria: 1. Too unwell to take part (judged by the multi-disciplinary team in the hospital) 2. Insufficient concentration to take part in paper and pencil tests for 1 hour (judged by the multi-disciplinary team in the hospital) 3. Insufficient language comprehension to pass the first comprehension tests in the OCS (picture pointing) 4. Outside of 2 months of the stroke;Exclusion criteria: 1. Too unwell to take part (judged by the multi-disciplinary team in the hospital) 2. Insufficient concentration to take part in paper and pencil tests for 1 hour (judged by the multi-disciplinary team in the hospital) 3. Insufficient language comprehension to pass the first comprehension tests in the OCS (picture pointing) 4. Outside of 2 months of the stroke

Design outcomes

Primary

MeasureTime frame
NIHSS score measured at baseline, at 6 months post stroke;NIHSS score measured at baseline, at 6 months post stroke

Secondary

MeasureTime frame
Oxford Cognitive Screen and the Montreal Cognitive Assessment measured at baseline, at 6 months post stroke;Oxford Cognitive Screen and the Montreal Cognitive Assessment measured at baseline, at 6 months post stroke

Countries

United Kingdom

Contacts

Public Contact; ;

;

;;

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026