Evaluation of a training pogramm for patients with coronary heart disease

Evaluation of a training pogramm for patients with coronary heart disease - KHK-Schulung

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00000394

Enrollment

406

Registered

2010-05-18

Start date

2010-02-03

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

coronary heart disease I25

Interventions

Group 1: Patients take part in the training program. The intervention includes in line with other recognized training in disease management programs, the following measures: • Patients attending a tra

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18-90 years 2. Patients with with coronary heart disease (in accordance with RSAV) 3. Ergometry within last 12 weeks 4. Ergometry in accordance with quality standards of the German society for research of cardiovascular diseases 5. ergometric achived power level of minimal 2 minutes 75 watt 6.Willingness and possibility to attend the training

Exclusion criteria

Exclusion criteria: 1. Patients, which are not able to answer questions of the questionnaires independently 2. Severe disease at final stage 3. Life expectancy under 6 months 4. Psychosis , severe dementia, nonexistence of contractual capability 5. Alcohol, drug and medication abuse 6. Participation on other studies

Design outcomes

Secondary

Measure	Time frame
1st Improve awareness of risk factors. Here is a significant improvement in Bochum assessment questionnaire expected. 2nd Improve the ergometric performance (a minute longer at the maximum level). 3rd Improvement of risk factors (self-report) 4th Improve emergency skills (self report) 5th report reduction in the number of cardiovascular endpoints (MI, bypass op, percutaneous coronary intervention, hospitalization because of CHD> 2 days) (self report) 6th Increasing the number of heart group participants (self report) 7th Reduction in body weight	—

Measure

Time frame

1st Improve awareness of risk factors. Here is a significant improvement in Bochum assessment questionnaire expected. 2nd Improve the ergometric performance (a minute longer at the maximum level). 3rd Improvement of risk factors (self-report) 4th Improve emergency skills (self report) 5th report reduction in the number of cardiovascular endpoints (MI, bypass op, percutaneous coronary intervention, hospitalization because of CHD> 2 days) (self report) 6th Increasing the number of heart group participants (self report) 7th Reduction in body weight

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Primary

Measure	Time frame
It will be tested two primary endpoints: 1st Improving physical activity daily 6 months after patients include in the study. Here, the intervention effect is expected from at least two hours per week times more activity (17% improvement in the Freiburg activity questionnaire). 2nd Improvement of disease-related quality of life 6 months after patients include in the study. Here, the intervention effect is expected by at least 0.5 points (10%) improvement in MacNew questionnaire.	—

Measure

Time frame

It will be tested two primary endpoints: 1st Improving physical activity daily 6 months after patients include in the study. Here, the intervention effect is expected from at least two hours per week times more activity (17% improvement in the Freiburg activity questionnaire). 2nd Improvement of disease-related quality of life 6 months after patients include in the study. Here, the intervention effect is expected by at least 0.5 points (10%) improvement in MacNew questionnaire.

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Countries

Germany

Contacts

Public ContactMartin Dürsch

Schwerpunktpraxis für Kardiologie / Angiologie

martin@familie-duersch.de0 69 / 61 09 200

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026