Effectiveness of a trans-sectoral gender-specific intervention to improve health behavior in rehabilitants with coronary heart disease.

Not Applicable

• Conditions: Percutaneous coronary interventionBypass-OP; I20.8; Other forms of angina pectoris

• Registration Number: DRKS00003568
• Lead Sponsor: Charité - Universitätsmedizin Berlin, Lehrstuhl für Versorgungssystemforschung

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-02-22
• Study Completion: 2014-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 545

Inclusion Criteria

After ACS, Bypass-OP, PCI.

Exclusion Criteria

Lack capacity to consent, lack of language skills.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change and continuity in the areas of physical activity, dietary habits, smoking, mental health, compliance to medication. Self-reported questionnaire at begin, end of rehabilitation and follow-up at 6 and 12 month after the end of rehabilitation.

Secondary Outcome Measures

Name	Time	Method
Regulation of blood pressure, blood glucose, blood cholesteron. Collection of clinical parameters at begin and end of rehabilitation. Self-reported questionnaire at begin and end of rehabilitation as well as follow-up at 6 and 12 month after end of rehabilitation.