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Cardiovascular Rehabilitation - Effectiveness of the Tulppa Program

Primary Purpose

Coronary Heart Disease

Status
Active
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Tulppa rehabilitation
Sponsored by
Rehabilitation Foundation, Finland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Heart Disease focused on measuring Rehabilitation, Coronary heart disease, Cardiovascular diseases, Risk factors, Life-style changes, Efficacy

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Study group: Patients diagnosed with coronary heart disease taking part in the Tulppa cardiac rehabilitation program at Pirkanmaa, South Karelia and Päijät-Häme health districts
  • Control group: Patients diagnosed with coronary heart disease, living in the area of Turku or Hyvinkää which are health districts that do not provide Tulppa rehabilitation.

Exclusion Criteria:

  • Acute and severe mental health problems, alcohol abuse, major limitations in physical activities

Sites / Locations

  • Rehabilitation Foundation

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Tulppa rehabilitation

Control group

Arm Description

8-10 weekly 3-hour group sessions and two follow-up sessions (6 and 12 months).

Control group does not receive Tulppa rehabilitation during the study.

Outcomes

Primary Outcome Measures

Health related quality of life
Health related quality of life is assessed with the finnish version of RAND-36-Item Health Survey (36-Item Short Form Survey Instrument - SF-36; Aalto, Aro & Teperi, 1999). The RAND-36 is a generic health-related survey consisting of 36 items with eight sub-scales: 1. general health, 2. bodily pain, 3. physical functioning, 4. role limitations/physical, 5. role limitations/emotional, 6. vitality, 7. mental health, and 8. social functioning. The total score is a sum of the eight subscales and the range is 0 - 100. Higher scores on the scale indicate a better quality of life.
Modified North Karelia CVD risk score
The limit values to calculate the CVD risk score were originally developed during the North Karelia project (Puska et al., 2009) and were further elaborated by Ketola (2001). The modified CVD risk score consists of six risk factors: Body mass index (BMI) Smoking Physical inactivity Systolic blood pressure Diastolic blood pressure Total cholesterol. The total score of the index is a sum of the 6 risk factors and the range is 0-16, the cut-off point indicating high risk of CVD is 4.5. Higher scores on the scale indicate a higher risk of cardiovascular disease. Subscore outcomes of the CVD risk score are defined as secondary outcome measures below.

Secondary Outcome Measures

The 6-Min Walk Test
The 6-min Walk Test (6MWT) measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface. The goal is for the individual to walk as far as possible in six minutes.
Blood pressure
Blood pressure is expressed in terms of the systolic and diastolic pressure and is measured in millimeters of mercury (mmHg).
Waist circumference
Waist circumference is measured halfway between the costal margin and iliac crest in centimeters.
Body mass index
The body mass index (BMI) is calculated as weight in kilograms divided by height in meters squared (kg/m2).
Lipid profile
Triglycerides, LDL-, HDL- and total cholesterol level will be measured with laboratory test
Blood glucose level
Fasting plasma glucose (mmol/l) will be measured with laboratory test
Physical inactivity
Physical inactivity is assessed with one question about the frequency per week of physical exercise causing swetting and /or some shortness of breath (1 = 3 or more times/week, 2 = 1-2 times/week, 3 = 1 time/week, 4 = sometimes, 5 = never)
Smoking
Smoking is evaluated with one question about number of cigarettes/day (0 = not at all...8 = 30 or more cigarettes/day)
Alcohol use
Alcohol use is measured with two questions: How often do you have drinks containing alcohol? (0 = never, 1 = monthly or less, 2 = 2-4 times a month, 3 = 2-3 times a week, 4 = 4 times a week or more) How many drinks containing alcohol do you have on a typical day when you are drinking? (1 = 1-2 drinks, 2 = 3-4, 3 = 5-6, 4 = 7-9, 5 = 10 drinks or more)
Dietary habits
Dietary habits are evaluated with 3 questions: Do you eat regular meals? (2 = yes, 1 = I don´t know, 0 = no) Do you use low-fat foods? (2 = yes, 1 = I don´t know, 0 = no) Do you eat enough good / healthy fat? (2 = yes, 1 = I don´t know, 0 = no)
Depression
Depression will be measured using The finnish Depression Scale DEPS (Salokangas, R. K., Poutanen, O & Stengard, E.,1995). 10 items, the items are rated from 0 to 3 (0 = not at all... ...3 = very much) and the range of the total score is 0-30. Higher scores on the scale indicate a higher probability of depression.
Anxiety
Anxiety will be assessed with the state-anxiety sub-scale of the Endler Multidimensional Anxiety Scales (EMAS-State) (Endler, N. S., Parker, J. D. A., Bagby, R. M., & Cox, B. J., 1991). The State-anxiety sub-scale consists of 20 items evaluated on a five-point Likert scale (score range 20-100). EMAS-State assesses two components of state-anxiety : a cognitive worry component and an autonomic-emotional component. Both components consist of ten items. In this study the 10 items of a cognitive worry component is used. Higher scores indicate a higher level of cognitive worry.

Full Information

First Posted
January 10, 2018
Last Updated
November 2, 2021
Sponsor
Rehabilitation Foundation, Finland
Collaborators
Finnish Heart Association
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1. Study Identification

Unique Protocol Identification Number
NCT03437616
Brief Title
Cardiovascular Rehabilitation - Effectiveness of the Tulppa Program
Official Title
Cardiovascular Rehabilitation - Effectiveness of the Tulppa Program - a Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Active, not recruiting
Study Start Date
February 19, 2018 (Actual)
Primary Completion Date
December 14, 2020 (Actual)
Study Completion Date
December 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rehabilitation Foundation, Finland
Collaborators
Finnish Heart Association

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
This study investigates the effectiveness of a Finnish Tulppa outpatient rehabilitation program. Tulppa is a group-based secondary prevention program for patients with vascular diseases. The program is developed by the Finnish Heart Association. The intervention is implemented at the local primary health care centers in 12 health districts in Finland. A longitudinal controlled study is used to investigate the effects of the intervention on participants' level of cardiovascular risk factors (e.g. lipids, blood pressure, body mass index), functional capacity (e.g. 6 minute walk test), life style as well as psychosocial factors (e.g. smoking, diet, physical activity, health-related quality of life and depression). The data will be collected at baseline (i.e. before the intervention), and 6 and 12 months after the intervention started. The participants (n = 300) are patients diagnosed with coronary heart disease. The study group (n = 150) is recruited from participants of Tulppa rehabilitation in three health care districts (Pirkanmaa, South Karelia, Päijät-Häme). The control group (n = 150) is recruited from two health care districts (Turku and Hyvinkää) that do not provide Tulppa rehabilitation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease
Keywords
Rehabilitation, Coronary heart disease, Cardiovascular diseases, Risk factors, Life-style changes, Efficacy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Longitudinal controlled study: The intervention group (n=150) participates in Tulppa rehabilitation program and the control group (n=150) do not participate in Tulppa rehabilitation.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tulppa rehabilitation
Arm Type
Experimental
Arm Description
8-10 weekly 3-hour group sessions and two follow-up sessions (6 and 12 months).
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Control group does not receive Tulppa rehabilitation during the study.
Intervention Type
Behavioral
Intervention Name(s)
Tulppa rehabilitation
Intervention Description
The intervention includes health education on e.g. healthy diet, weight management, physical activity and psychosocial coping as well as peer discussions and physical exercises.
Primary Outcome Measure Information:
Title
Health related quality of life
Description
Health related quality of life is assessed with the finnish version of RAND-36-Item Health Survey (36-Item Short Form Survey Instrument - SF-36; Aalto, Aro & Teperi, 1999). The RAND-36 is a generic health-related survey consisting of 36 items with eight sub-scales: 1. general health, 2. bodily pain, 3. physical functioning, 4. role limitations/physical, 5. role limitations/emotional, 6. vitality, 7. mental health, and 8. social functioning. The total score is a sum of the eight subscales and the range is 0 - 100. Higher scores on the scale indicate a better quality of life.
Time Frame
Changes between baseline, 6 months and 12 months
Title
Modified North Karelia CVD risk score
Description
The limit values to calculate the CVD risk score were originally developed during the North Karelia project (Puska et al., 2009) and were further elaborated by Ketola (2001). The modified CVD risk score consists of six risk factors: Body mass index (BMI) Smoking Physical inactivity Systolic blood pressure Diastolic blood pressure Total cholesterol. The total score of the index is a sum of the 6 risk factors and the range is 0-16, the cut-off point indicating high risk of CVD is 4.5. Higher scores on the scale indicate a higher risk of cardiovascular disease. Subscore outcomes of the CVD risk score are defined as secondary outcome measures below.
Time Frame
Changes between baseline, 6 months and 12 months
Secondary Outcome Measure Information:
Title
The 6-Min Walk Test
Description
The 6-min Walk Test (6MWT) measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface. The goal is for the individual to walk as far as possible in six minutes.
Time Frame
Changes between baseline, 6 months and 12 months
Title
Blood pressure
Description
Blood pressure is expressed in terms of the systolic and diastolic pressure and is measured in millimeters of mercury (mmHg).
Time Frame
Changes between baseline, 6 months and 12 months
Title
Waist circumference
Description
Waist circumference is measured halfway between the costal margin and iliac crest in centimeters.
Time Frame
Changes between baseline, 6 months and 12 months
Title
Body mass index
Description
The body mass index (BMI) is calculated as weight in kilograms divided by height in meters squared (kg/m2).
Time Frame
Changes between baseline, 6 months and 12 months
Title
Lipid profile
Description
Triglycerides, LDL-, HDL- and total cholesterol level will be measured with laboratory test
Time Frame
Changes between baseline, 6 months and 12 months
Title
Blood glucose level
Description
Fasting plasma glucose (mmol/l) will be measured with laboratory test
Time Frame
Changes between baseline, 6 months and 12 months
Title
Physical inactivity
Description
Physical inactivity is assessed with one question about the frequency per week of physical exercise causing swetting and /or some shortness of breath (1 = 3 or more times/week, 2 = 1-2 times/week, 3 = 1 time/week, 4 = sometimes, 5 = never)
Time Frame
Changes between baseline, 6 months and 12 months
Title
Smoking
Description
Smoking is evaluated with one question about number of cigarettes/day (0 = not at all...8 = 30 or more cigarettes/day)
Time Frame
Changes between baseline, 6 months and 12 months
Title
Alcohol use
Description
Alcohol use is measured with two questions: How often do you have drinks containing alcohol? (0 = never, 1 = monthly or less, 2 = 2-4 times a month, 3 = 2-3 times a week, 4 = 4 times a week or more) How many drinks containing alcohol do you have on a typical day when you are drinking? (1 = 1-2 drinks, 2 = 3-4, 3 = 5-6, 4 = 7-9, 5 = 10 drinks or more)
Time Frame
Changes between baseline, 6 months and 12 months
Title
Dietary habits
Description
Dietary habits are evaluated with 3 questions: Do you eat regular meals? (2 = yes, 1 = I don´t know, 0 = no) Do you use low-fat foods? (2 = yes, 1 = I don´t know, 0 = no) Do you eat enough good / healthy fat? (2 = yes, 1 = I don´t know, 0 = no)
Time Frame
Changes between baseline, 6 months and 12 months
Title
Depression
Description
Depression will be measured using The finnish Depression Scale DEPS (Salokangas, R. K., Poutanen, O & Stengard, E.,1995). 10 items, the items are rated from 0 to 3 (0 = not at all... ...3 = very much) and the range of the total score is 0-30. Higher scores on the scale indicate a higher probability of depression.
Time Frame
Changes between baseline, 6 months and 12 months
Title
Anxiety
Description
Anxiety will be assessed with the state-anxiety sub-scale of the Endler Multidimensional Anxiety Scales (EMAS-State) (Endler, N. S., Parker, J. D. A., Bagby, R. M., & Cox, B. J., 1991). The State-anxiety sub-scale consists of 20 items evaluated on a five-point Likert scale (score range 20-100). EMAS-State assesses two components of state-anxiety : a cognitive worry component and an autonomic-emotional component. Both components consist of ten items. In this study the 10 items of a cognitive worry component is used. Higher scores indicate a higher level of cognitive worry.
Time Frame
Changes between baseline, 6 months and 12 months
Other Pre-specified Outcome Measures:
Title
Family support
Description
Partner support will be measured with a Finnish 12-item Family Support (FS) scale (Julkunen & Greenglass, 1989; Gustavsson-Lilius M., Julkunen J., & Hietanen P., 2007). The items are rated using a five-step Likert scale (1 = completely disagree… 5 = completely agree) and the range of the total score is 12 - 60. The sum-score of the scale reflects the respondents' perceived degree of emotional and instrumental support received from other family members. Higher scores on the scale indicates higher amount of perceived support from the family.
Time Frame
Baseline, 6 months and twelve months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Study group: Patients diagnosed with coronary heart disease taking part in the Tulppa cardiac rehabilitation program at Pirkanmaa, South Karelia and Päijät-Häme health districts Control group: Patients diagnosed with coronary heart disease, living in the area of Turku or Hyvinkää which are health districts that do not provide Tulppa rehabilitation. Exclusion Criteria: Acute and severe mental health problems, alcohol abuse, major limitations in physical activities
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erja Poutianen, PhD
Organizational Affiliation
Rehabilitation Foundation
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mila Gustavsson-Lilius, PhD
Organizational Affiliation
Rehabilitation Foundation
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Piia Pietilä, MA
Organizational Affiliation
Rehabilitation Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehabilitation Foundation
City
Helsinki
State/Province
Malminkartano
ZIP/Postal Code
00410
Country
Finland

12. IPD Sharing Statement

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Cardiovascular Rehabilitation - Effectiveness of the Tulppa Program

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