- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03730701
Make my Day - Primary Prevention of Stroke
"Make my Day"- Incorporating Healthy Activity Patterns: A Person-centered, Digital Prevention Program to Support Health Among Persons at Risk for Stroke
Study Overview
Status
Intervention / Treatment
Detailed Description
The study is a randomized controlled pilot trial evaluating the feasibility of a digitally augmented person-centered stroke prevention program with a focus on primary prevention. The program is aiming to enable lifestyle change and to promote healthy activity patterns to decrease risk factors for stroke and in that way prevent future stroke. With activity patterns (individual actions and behaviour) in everyday life we mean a persons overall lifestyle that may or may not contribute to health.
The prevention program is a theoretically grounded, complex intervention tested against a control-group that are receiving usual care. The prevention program is based on activities in people's everyday lives and integrates health and well-being with what people do, as well as with what they want or need to do, in order to thrive and live well. Lifestyle change refers to a conscious change of behaviour and everyday activities in order to promote health. The process of changing behaviour results from an interaction between the person (eg, self-efficacy), the environment (support and material) and the action. In the project, the key behavioural change technique is incorporating engaging everyday activities (EEAs) that contribute to a healthy lifestyle. This might include changing the form of current EEAs or finding new health-promoting EEAs.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Stockholms Län
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Huddinge, Stockholms Län, Sweden, 14183
- Karolinska Institutet
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Persons with increased risk for stroke according to Stroke risk score card
- Persons motivated for participating in an intense digital lifestyle prevention (including the use of a mobile phone with the function to download and use apps),
Exclusion Criteria:
- Persons having had a stroke or TIA
- Persons with a diagnosis of dementia or cognitive impairment
- Drug abuse
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Prevention treatment group
Prevention program with 10 week blended intervention utilizing both a digital health app, group-sessions with peers and a interprofessional team of health-care workers chairing 5+1 themed group-sessions as support to change lifestyle habits in to a pattern of activities (behaviors and actions) in everyday life that can promote health and wellbeing and decrease risk for stroke.
Lifestyle analysis and stroke risk screening before, at follow up and 12 months after the prevention program.
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The prevention program include individual and group intervention sessions supported by a digital platform.
The program will be personally tailored in relation to what the person needs and what to change and the individuals rediness for change.
The digital platform will support the person during and in between sessions by prompting goals and goal-fulfilment, logging activities, step counts and provide a forum for sharing and reflection.
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No Intervention: Standard treatment group
Usal care in Swedish primary health care.
In addition a Lifestyle analysis and stroke risk screening before, at follow up and 12 months after the prevention program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stroke risk score card
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Through the stroke risk score card estimate change in risk for Stroke and how high this risk are. Three colums with different colours. Red, yellow and green. Red is High risk, Yellow is Caution, and Green is Low risk. In total there is 8 points per column. High risk: >3 red points: Ask about stroke prevention right away. Caution: 4-6: A good start. Work on reducing risk. Low risk: 6-8: You're doing very well at controlling stroke risk. |
Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Healthy Activity patterns (PPR profile)
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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PPRP (Daily Experiences of Pleasure, Productivity, and Restoration Profile) is a activity-diary where change is meant to be measured regarding activity patterns in everyday life.
Experiences are scored as 1-7 in four domains (Pleasure, Productivity, Restoration and Health promotion).
For example the domain of health promotion is scored as 1 (very unhealthy) to 7 (very healthy) in regards to different engagements in everyday life.
The higher the value the better.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Questions of Lifestyle habits
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Measuring change in lifestyle habits with a self-percieved questionnaire with open questions and estimations of different lifestyle habits in everyday life regarding dietary, smoking, alcohol, physical activity habits. Participants selects an option on each question or writes an estimated number or answer on what and how they usually do regarding each lifestyle habit. For example if they are or have been smoking and how much. Example of answers options:
And on alcohol consumption. Question: How many standard glases do you drink a normal week? Answer with a self-percieved number, no fixed response options. |
Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Canadian Occupational Performance Measurement (COPM)
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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COPM is a client-centered, semi-structured interview assessment that enables the person to identify and prioritize areas of improvement in everyday life.
To support goal-setting, defined areas is scored between 0-10 guiding prioritizations of areas of which is scored in regards to performance and satisfaction, also scored between 0-10.
Where a higher value is better experience of performance and satisfaction of occupations.
Mean change will be measured.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Weight
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Measure in kilograms with a scale.
Measure includes observation of changes.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Blood pressure
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Measure systolic and diastolic blood pressure with blood pressure machine.
Measure includes observation of changes.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Occupational Balance (OBQ4)
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Self-percieved questionnaire of balance in and between occupations in everyday life.
13 questions.
Answers between 1-4 where 1 is Do not agree at all, And 4 is Agree very much.
Measure includes observation of changes.
Where a higher value is better.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Motivation for lifestyle changes
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Measure motivation for lifestyle changes with questionnare on a scale from 1 to 5 where 1 is does not fit at all and 5 is fits very well. Points: 20 - 25 points: High level of motivation for change. 15 - 20 points: Moderat level of motivation to change. 10 - 15 points: Low level of motivation to change. Below 10 points: Very low motivation to change. The higher value the better. Measure includes observation of changes. |
Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Lisat-11
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Questionnaire on Life satisfaction with 11 questions with a scale 1-6. 1 means unsatisfied and 6 means very satisfied.
Where a higher value is better.
Measure includes observation of changes.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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EQ5D
Time Frame: Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Questionnaire of Quality of Life with two different parts.
Part one includes 5 domains scored from 1 to 3, where a higher value is worse.
For example "worry/depression" 1.
I am not worried/depressed) 2. I am worried or depressed to some degree.
3. I am very much worried and/or depressed.
The second part is a VAS-scale from 1 to 100, where a higher value is better state of health.
Measures includes observation of changes.
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Baseline, within a month after the intervention, 1 year follow-up after baseline.
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Ann-Helen Patomella, PhD, Karolinska Institutet
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MMDPrev1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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