Long-term Follow-up After Stroke (The LAST-long Trial)
NCT03859063 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 301
Last updated 2025-09-16
Summary
Despite the improved treatment of acute stroke over the past decades, those suffering from stroke still are at an increased risk of functional and cognitive decline in the long term. The most common consequences of stroke are functional impairments, cognitive impairments, depression and fatigue. These are also regarded as barriers to achieve optimal adherence to the guidelines regarding secondary prevention. The primary aim of this project is to evaluate the effectiveness of a multimodal individualized intervention to prevent functional decline in the long term after stroke.
Conditions
Interventions
- BEHAVIORAL
-
Intervention
Participants randomized to the intervention arm will be followed with monthly meetings by a stroke coordinator for 18 months. The stroke coordinator will assess the patients risk factors within the domains of physical function, cognitive function, social function, medication and lifestyle factors and make a treatment plan targeting the individual needs for further follow-up.
- BEHAVIORAL
-
Control
Community based follow-up as usual
Sponsors & Collaborators
-
St. Olavs Hospital
collaborator OTHER -
University Hospital, Akershus
collaborator OTHER -
Asker & Baerum Hospital
collaborator OTHER -
Alesund Hospital
collaborator OTHER -
Norwegian University of Science and Technology
lead OTHER
Principal Investigators
-
Jorunn Helbostad, phd prof · Norwegian University for Science and Technology
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-04-11
- Primary Completion
- 2024-09-30
- Completion
- 2024-12-31
Countries
- Norway
Study Locations
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