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NCT Number: NCT03437616

Cardiovascular Rehabilitation - Effectiveness of the Tulppa Program

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rehabilitation Foundation

Helsinki, Malminkartano, 00410, Finland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Tulppa rehabilitation

Behavioral

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 outcomes

  1. Health related quality of life

    Time frame: Changes between baseline, 6 months and 12 months

    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.

  2. Modified North Karelia CVD risk score

    Time frame: Changes between baseline, 6 months and 12 months

    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 outcomes

  1. The 6-Min Walk Test

    Time frame: Changes between baseline, 6 months and 12 months

    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.

  2. Blood pressure

    Time frame: Changes between baseline, 6 months and 12 months

    Blood pressure is expressed in terms of the systolic and diastolic pressure and is measured in millimeters of mercury (mmHg).

  3. Waist circumference

    Time frame: Changes between baseline, 6 months and 12 months

    Waist circumference is measured halfway between the costal margin and iliac crest in centimeters.

  4. Body mass index

    Time frame: Changes between baseline, 6 months and 12 months

    The body mass index (BMI) is calculated as weight in kilograms divided by height in meters squared (kg/m2).

  5. Lipid profile

    Time frame: Changes between baseline, 6 months and 12 months

    Triglycerides, LDL-, HDL- and total cholesterol level will be measured with laboratory test

  6. Blood glucose level

    Time frame: Changes between baseline, 6 months and 12 months

    Fasting plasma glucose (mmol/l) will be measured with laboratory test

  7. Physical inactivity

    Time frame: Changes between baseline, 6 months and 12 months

    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)

  8. Smoking

    Time frame: Changes between baseline, 6 months and 12 months

    Smoking is evaluated with one question about number of cigarettes/day (0 = not at all...8 = 30 or more cigarettes/day)

  9. Alcohol use

    Time frame: Changes between baseline, 6 months and 12 months

    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)
  10. Dietary habits

    Time frame: Changes between baseline, 6 months and 12 months

    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)

  11. Depression

    Time frame: Changes between baseline, 6 months and 12 months

    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.

  12. Anxiety

    Time frame: Changes between baseline, 6 months and 12 months

    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.

Other outcomes

  1. Family support

    Time frame: Baseline, 6 months and twelve months

    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.

Sponsors and collaborators

Lead sponsor

Rehabilitation Foundation, Finland

Other

Collaborators

  • Finnish Heart Association

Registry information

Official study title

Cardiovascular Rehabilitation - Effectiveness of the Tulppa Program - a Controlled Study

Important dates

Study start
2018
Primary completion
2020
Study completion
2029
First posted
Feb 19, 2018
Registry last updated
Jul 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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