search
Back to results

Life After STroke - the LAST Study (LAST)

Primary Purpose

Cerebral Infarction, Cerebral Hemorrhage

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Long term follow up by a coordinating physiotherapist
Standard care
Sponsored by
Norwegian University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Infarction focused on measuring Stroke, Physiotherapy, Motor training, Rehabilitation

Eligibility Criteria

18 Years - 95 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of stroke according to WHO's definition of stroke
  • Living in the city of Trondheim or the municipalities of Asker or Bærum
  • Included 2.5 - 4 months after stroke
  • Modified Rankin Scale 0 - 4
  • Living at home
  • Mini Mental State Examination > 20 or > 16 if aphasia
  • Provide informed consent

Exclusion Criteria:

  • Are already included in the study
  • Are included in other experimental studies
  • Unstable coronary function
  • Uncompensated heartfailure
  • Other diseases that make it difficult to complete the intervention

Sites / Locations

  • Bærum Hospital
  • St. Olavs Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Long term follow up program

Standard care

Arm Description

Outcomes

Primary Outcome Measures

Motor Assessment Scale
A measure of over all motor function

Secondary Outcome Measures

Barthel Index
A measure of activities of daily living
Modified Rankin Scale
A measure of dependency/independency
Berg Balance Scale
A measure of balance related to basic movement tasks
Timed Up and Go
A measure of balance related to transfer and walking
Sit to stand test
A measure of dynamic muscle strength according to a sit to stand task
Six minute walk test
A measure of endurance
Stroke Impact Scale
A measure of health related quality of life after stroke
EuroQol 5D
A simple measure of health related quality of life for the general population
Fatigue Severity Scale
A measure of the presence of fatigue
One simple question on fatigue from the HUNT3 questionnaire
A simple question used to assess tiredness in teh general Norwegian population
Hospital Anxiety and Depression Scale
A measure of anxiety and depression
Mini Mental State Examination
A measure of cognitive function
Montreal Cognitive Assessment
A measure of cognitive function related to vascular dementia
falls
Serious falls will be recorded from the patients hospital records
Readmission to hospital
Number of readmissions to hospital will be recorded from the patients medical records
Death
Information about death will be collected from the Norwegain Death Registry
Fractures
Information about fractures during follow up will be collected from the patients medical records
Cardiovascular events
Information about any cardiovascular events will be collected from the patients medical record
Cerebrovascular events
Information about any cerebrovascular events during follow up will be collected from teh patient's medical records
International Physical Activity Questionnaire
A measure of physical activity over the last week
Physical activity assessed by ActivPAL sensor system
A sensor system to assess the amount of physical activity during a 4-7 day period
Three simple questions on physical activity from the HUNT questionnaire
A simple measure of physical activity
Health costs
Information about the use of health services will be collected by reviewing the patients' hospital records and records in primary health care system.
National Institutes of Health Stroke Scale
A measure of stroke severity
Modified Ashworth Scale
A measure to rate the degree of spasticity after stroke
Gait speed
A simple measure of maximum gait speed across a 10 metres distance
Trailmaking test A and B
A simple measure of executive cognitive function
DS-14
A standard assessment of negative affectivity, social inhibition, and type D personality, which might be related to poor cardiovascular prognosis.

Full Information

First Posted
October 31, 2011
Last Updated
April 9, 2020
Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital, Asker & Baerum Hospital, The Research Council of Norway, Helse Midt-Norge
search

1. Study Identification

Unique Protocol Identification Number
NCT01467206
Brief Title
Life After STroke - the LAST Study
Acronym
LAST
Official Title
Life After STroke - the LAST Study. A Norwegian Multi Centre Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
November 2011 (Actual)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital, Asker & Baerum Hospital, The Research Council of Norway, Helse Midt-Norge

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The LAST study is a Norwegian multi site randomised controlled trial that intends to assess the effect of a long term follow up program after stroke. The program consists of a coordinating physiotherapist who will encourage and motivate included patients to perform at least 60 minutes of intensive motor training every week and 30 minutes of physical activity every day for 18 months after inclusion. The primary hypothesis is that patients receiving a long term follow up program after stroke will have better motor function at end of follow up than patients receiving standard care. A total of 390 home dwelling stroke patients living in the municipality of Trondheim, Asker and Bærum will be included at the out-patient clinic at St. Olavs Hospital or Bærum Hospital three months after their stroke. Included patients will be randomised to an intervention group receiving the long term follow up program or to a control group receiving standard care. Motor function, mental health and physical functioning in daily life will be assessed at inclusion and 18 months later. The LAST study is funded by the Norwegian Research Council, the Norwegian University of Science and Technology and the Central Norway Regional Health Authority and will conclude at the end of 2015.
Detailed Description
Supplement to the Life After Stroke - the LAST study ClinicalTrials.gov ID: NCT01467206 Changes in the planned statistical analysis, November 9, 2015 The original plan for statistical analysis was published in; Askim T, Langhammer B, Ihle-Hansen H, Magnussen J, Engstad T, Indredavik B. A Long-Term Follow-Up Programme for Maintenance of Motor Function after Stroke: Protocol of the life after Stroke-The LAST Study. Stroke Res Treat. 2012;2012:392101. doi: 10.1155/2012/392101. Epub 2012 Nov 22. Original plan for statistical analysis Reporting will follow the CONSORT statement for parallel group randomized trials [40]. Descriptive statistics will be performed in order to present the population and the characteristic of the two groups. All analyses will be analysed as intention-to-treat analysis according to the CONSORT instructions. Analysis of covariance (ANCOVA) will be used to study differences between groups according to the primary endpoint, motor assessment scale at 18 months after inclusion. The ANCOVA model will include stroke severity, age, pre stroke disability, treatment group, and motor function at baseline as covariates. Mann-Whitney U test will be used for secondary data not being normal distributed. In all analyses we will control for potential confounding factors, investigate effect modifications, and present both unadjusted and adjusted effects with 95% confidence intervals. Subanalysis will be performed according to the stratification variables (stroke severity, age above 80 and recruitment site) to explore trends within subgroups of patients. Revised plan for statistical analysis Reporting will follow the CONSORT statement for parallel group randomized trials [40]. Descriptive statistics will be performed in order to present the population and the characteristic of the two groups. All analyses will be analysed as intention-to-treat analysis according to the CONSORT instructions. Analysis of covariance (ANCOVA) will be used to study differences between groups according to the primary endpoint, motor assessment scale at 18 months after inclusion. The ANCOVA model will include stroke severity, age, pre stroke disability, treatment group, and motor function at baseline as covariates. Similar ANCOVA analyses will be used for the relevant secondary endpoints. Mann-Whitney U test will be used for secondary data not being normal distributed. Subanalysis will be performed according to the stratification variables (stroke severity, age above 80 and recruitment site), gender, and cognitive status (Mini Mental State below 25), to explore trends within subgroups of patients. Missing values will be handled using single imputation (typically for items on instrument scales), or by multiple imputation, as appropriate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Infarction, Cerebral Hemorrhage
Keywords
Stroke, Physiotherapy, Motor training, Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
380 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Long term follow up program
Arm Type
Experimental
Arm Title
Standard care
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Long term follow up by a coordinating physiotherapist
Intervention Description
Monthly meetings with an coordinating physiotherapist who motivate and encourage the patient to do 60 minutes of weekly exercise and 30 minutes of daily physical activity
Intervention Type
Behavioral
Intervention Name(s)
Standard care
Intervention Description
Standard care as it is given to all stoke patients after stroke
Primary Outcome Measure Information:
Title
Motor Assessment Scale
Description
A measure of over all motor function
Time Frame
18 months after inclusion
Secondary Outcome Measure Information:
Title
Barthel Index
Description
A measure of activities of daily living
Time Frame
18 months follow up
Title
Modified Rankin Scale
Description
A measure of dependency/independency
Time Frame
18 months follow up
Title
Berg Balance Scale
Description
A measure of balance related to basic movement tasks
Time Frame
18 months follow up
Title
Timed Up and Go
Description
A measure of balance related to transfer and walking
Time Frame
18 months follow up
Title
Sit to stand test
Description
A measure of dynamic muscle strength according to a sit to stand task
Time Frame
18 months follow up
Title
Six minute walk test
Description
A measure of endurance
Time Frame
18 months follow up
Title
Stroke Impact Scale
Description
A measure of health related quality of life after stroke
Time Frame
18 months follow up
Title
EuroQol 5D
Description
A simple measure of health related quality of life for the general population
Time Frame
18 months follow up
Title
Fatigue Severity Scale
Description
A measure of the presence of fatigue
Time Frame
18 months follow up
Title
One simple question on fatigue from the HUNT3 questionnaire
Description
A simple question used to assess tiredness in teh general Norwegian population
Time Frame
18 months follow up
Title
Hospital Anxiety and Depression Scale
Description
A measure of anxiety and depression
Time Frame
18 months follow up
Title
Mini Mental State Examination
Description
A measure of cognitive function
Time Frame
18 months follow up
Title
Montreal Cognitive Assessment
Description
A measure of cognitive function related to vascular dementia
Time Frame
18 months follow up
Title
falls
Description
Serious falls will be recorded from the patients hospital records
Time Frame
6, 12 and 18 months
Title
Readmission to hospital
Description
Number of readmissions to hospital will be recorded from the patients medical records
Time Frame
6, 12 and 18 months
Title
Death
Description
Information about death will be collected from the Norwegain Death Registry
Time Frame
6, 12 and 18 months
Title
Fractures
Description
Information about fractures during follow up will be collected from the patients medical records
Time Frame
6, 12 and 18 months
Title
Cardiovascular events
Description
Information about any cardiovascular events will be collected from the patients medical record
Time Frame
6, 12 and 18 months
Title
Cerebrovascular events
Description
Information about any cerebrovascular events during follow up will be collected from teh patient's medical records
Time Frame
6, 12 and 18 months
Title
International Physical Activity Questionnaire
Description
A measure of physical activity over the last week
Time Frame
6, 12 and 18 months
Title
Physical activity assessed by ActivPAL sensor system
Description
A sensor system to assess the amount of physical activity during a 4-7 day period
Time Frame
6, 12 and 18 months
Title
Three simple questions on physical activity from the HUNT questionnaire
Description
A simple measure of physical activity
Time Frame
18 months
Title
Health costs
Description
Information about the use of health services will be collected by reviewing the patients' hospital records and records in primary health care system.
Time Frame
6, 12 and 18 months
Title
National Institutes of Health Stroke Scale
Description
A measure of stroke severity
Time Frame
18 months follow up
Title
Modified Ashworth Scale
Description
A measure to rate the degree of spasticity after stroke
Time Frame
18 months follow up
Title
Gait speed
Description
A simple measure of maximum gait speed across a 10 metres distance
Time Frame
18 months follow up
Title
Trailmaking test A and B
Description
A simple measure of executive cognitive function
Time Frame
18 months follow up
Title
DS-14
Description
A standard assessment of negative affectivity, social inhibition, and type D personality, which might be related to poor cardiovascular prognosis.
Time Frame
18 months follow up
Other Pre-specified Outcome Measures:
Title
VO2-peak
Description
VO2-peak is obtained by use of a symptom limited treadmill test to measure cardiovascular fitness. This measure is only used in the Trondheim arm of the study
Time Frame
18 months follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
95 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of stroke according to WHO's definition of stroke Living in the city of Trondheim or the municipalities of Asker or Bærum Included 2.5 - 4 months after stroke Modified Rankin Scale 0 - 4 Living at home Mini Mental State Examination > 20 or > 16 if aphasia Provide informed consent Exclusion Criteria: Are already included in the study Are included in other experimental studies Unstable coronary function Uncompensated heartfailure Other diseases that make it difficult to complete the intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bent Indredavik, Prof
Organizational Affiliation
National Taiwan Normal University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Torunn Askim, PhD
Organizational Affiliation
National Taiwan Normal University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bærum Hospital
City
Sandvika
Country
Norway
Facility Name
St. Olavs Hospital
City
Trondheim
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
23227428
Citation
Askim T, Langhammer B, Ihle-Hansen H, Magnussen J, Engstad T, Indredavik B. A Long-Term Follow-Up Programme for Maintenance of Motor Function after Stroke: Protocol of the life after Stroke-The LAST Study. Stroke Res Treat. 2012;2012:392101. doi: 10.1155/2012/392101. Epub 2012 Nov 22.
Results Reference
background
PubMed Identifier
29284737
Citation
Askim T, Langhammer B, Ihle-Hansen H, Gunnes M, Lydersen S, Indredavik B; LAST Collaboration Group. Efficacy and Safety of Individualized Coaching After Stroke: the LAST Study (Life After Stroke): A Pragmatic Randomized Controlled Trial. Stroke. 2018 Feb;49(2):426-432. doi: 10.1161/STROKEAHA.117.018827. Epub 2017 Dec 28.
Results Reference
result
PubMed Identifier
32252739
Citation
Dohl O, Halsteinli V, Askim T, Gunnes M, Ihle-Hansen H, Indredavik B, Langhammer B, Phan A, Magnussen J. Factors contributing to post-stroke health care utilization and costs, secondary results from the life after stroke (LAST) study. BMC Health Serv Res. 2020 Apr 6;20(1):288. doi: 10.1186/s12913-020-05158-w.
Results Reference
result
PubMed Identifier
34184251
Citation
Saunders DH, Mead GE, Fitzsimons C, Kelly P, van Wijck F, Verschuren O, Backx K, English C. Interventions for reducing sedentary behaviour in people with stroke. Cochrane Database Syst Rev. 2021 Jun 29;6(6):CD012996. doi: 10.1002/14651858.CD012996.pub2.
Results Reference
derived
PubMed Identifier
31374191
Citation
Gunnes M, Indredavik B, Langhammer B, Lydersen S, Ihle-Hansen H, Dahl AE, Askim T; LAST Collaboration group. Associations Between Adherence to the Physical Activity and Exercise Program Applied in the LAST Study and Functional Recovery After Stroke. Arch Phys Med Rehabil. 2019 Dec;100(12):2251-2259. doi: 10.1016/j.apmr.2019.04.023. Epub 2019 Jul 30.
Results Reference
derived

Learn more about this trial

Life After STroke - the LAST Study

We'll reach out to this number within 24 hrs