Ignite Creation Date:
2024-05-06 @ 3:45 PM
Last Modification Date:
2024-10-26 @ 1:56 PM
Study NCT ID:
NCT04746157
Status:
COMPLETED
Last Update Posted:
2024-03-15
First Post:
2020-12-18
Brief Title:
A Nursing Support Intervention-based Project for Stroke Survivors
Sponsor:
Institut de Recerca Biomèdica de Lleida
Organization:
Institut de Recerca Biomèdica de Lleida
Study Overview
Official Title:
A Nursing Support Intervention-based Project for Stroke Survivors to Improve Patient Centered Outcomes Measures
Status:
COMPLETED
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PROICTUS
Brief Summary:
Stroke is the second single most common cause of death and the main cause of disability in the European Union EU region Stroke victims face an uncertain future and a life severely affected by disability Although there have been many advances in scientific knowledge and innovation in stroke research improvements in stroke systems of care are still necessary to ensure patient outcomes and improve their quality of life after stroke The main goal of PROICTUS program pro in Greek means before and in Latin means forward movement is to evaluate a nursing support intervention to improve PROMS patient reported outcome measures and the quality of life in stroke survivors Patients will have a directly contact with the lead nurse by telephone so they will receive information about their disease their current situation given them a personalized care and resolving questions that are important for them in their new life situation
Detailed Description:
It is estimated that 6 months after stroke 45 of survivors have some type of functional dependence The impact of stroke is quantified in disability adjusted life-years DALYs where DALY is 1 year of healthy life lost Worldwide the average number of post stroke DALYs is projected to be 609 million by 2030 Although the incidence of stroke disease increases with age rates in young adults are rising suggesting a need for strategies to improve prevention Beyond vital prognosis stroke patients are also at increased risk of poor outcome within the first year of the event including re-hospitalization recurrent event dementia mild cognitive disorder depression and fatigue and all affect quality of life Given these observations an urgent development of acute care provision as well as resources for post-stroke therapeutic strategies are needed PROICTUS not only could improve PROMS patient reported outcome measures and quality of life it is also the tool to increase the adherence to the treatment reduce the risk factors and ensure an adequate secondary prevention Patients will be recruited from the emergency service of the Hospital in a period within 14 days from the index event Half of the selected participants will be part of the PROICTUS interventional project and the other half of the selected patients will receive the usual management All patients will be contacted by a phone call the PROICTUS project will be explained to both arms inform consent obtained and a blood extraction lipid profile and glycosylated haemoglobin will be performed Non interventional group will follow up usual medical care and they will not be contacted by the referent nurse for 12 months After 1 year of the stroke participants of the no intervention group will be contacted by phone and primary outcome measurements obtained
Interventional group will receive a second call 30 days after the stroke In the second call patients will get personalize information about hisher health situation and comprehensive individualized communication For that the main intervention will be direct contact with the lead nurse by telephoneemail
Basal evaluation will be assessed by five surveys PROMIS 57 Profile v21 the EQ-5D-5L survey of treatment adherence survey of adherence to the Mediterranean diet and the Stroke Riskometer These evaluation will be repeated at 90 days and 12 months after stroke This group will also have a tensiometer to measure pressure blood cardiac rate and detected arrhythmias Additionaly participants of this arm could call the nurse two days per week to ask her whatever they need
Acute ischemic stroke represents a very important and still to be solved health and social problem For that this project is a great challenge and many people would beneficiate of its progress
Interventional group will receive a second call 30 days after the stroke In the second call patients will get personalize information about hisher health situation and comprehensive individualized communication For that the main intervention will be direct contact with the lead nurse by telephoneemail
Basal evaluation will be assessed by five surveys PROMIS 57 Profile v21 the EQ-5D-5L survey of treatment adherence survey of adherence to the Mediterranean diet and the Stroke Riskometer These evaluation will be repeated at 90 days and 12 months after stroke This group will also have a tensiometer to measure pressure blood cardiac rate and detected arrhythmias Additionaly participants of this arm could call the nurse two days per week to ask her whatever they need
Acute ischemic stroke represents a very important and still to be solved health and social problem For that this project is a great challenge and many people would beneficiate of its progress
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None