Herrmann-Lingen, Christoph http://orcid.org/0000-0002-7813-7045
Albus, Christian
de Zwaan, Martina
Geiser, Franziska
Heinemann, Katrin
Hellmich, Martin
Michal, Matthias
Sadlonova, Monika
Tostmann, Ralf
Wachter, Rolf
Herbeck Belnap, Birgit
Clinical trials referenced in this document:
Documents that mention this clinical trial
Efficacy of team-based collaborative care for distressed patients in secondary prevention of chronic coronary heart disease (TEACH): study protocol of a multicenter randomized controlled trial
https://doi.org/10.1186/s12872-020-01810-9
Funding for this research was provided by:
Bundesministerium für Bildung und Forschung (01KG2011)
Projekt DEAL
Article History
Received: 2 November 2020
Accepted: 2 December 2020
First Online: 10 December 2020
Change Date: 23 December 2020
Change Type: Update
Change Details: The original publication was missing the supplementary file. The article has been updated to include this file.
Ethics approval and consents to participate
: This study protocol, Version 1.0, was approved by the Ethics Committee of the University of Göttingen Medical Center (#31/4/20) and all participating sites, i.e. the Ethics Committees at the Universities of Bonn (#347/20), Cologne (#20-1397_1), and Leipzig (#363/20-lk), the Medical University of Hannover (#9253_BO_K_2020), and the Medical Association of Rhineland-Palatinate (#2020-15252_1). Patient recruitment only started after ethical approval has become available at the respective sites. TEACH has a two-step enrollment process (see “InternalRef removed”). Study staff explains both the screening and study procedures to patients in detail, and gives patients ample time and opportunity to obtain answers to any open questions. Patients are informed that their participation is voluntary and that they may withdraw at any time without having to give reasons and without penalty or loss of benefits to which they are otherwise entitled. In addition, the patient receives a "Patient Information Sheet”, which contains all the important information about the study in writing. Written informed consent is obtained from each participant before any trial-related procedures are performed and patients receive a copy of the signed and dated written consent form.
: Not applicable.
: During the last 3 years, CHL has received lecture honoraria from Novartis and Pfizer and royalties for the German version of the Hospital Anxiety and Depression Scale from Hogrefe Huber Publishers. CA has received honoraria from Bayer Vital, UCB and Boehringer Ingelheim. MM has received lecture honoraria from DAIICHI SANKYO. RW has received honoraria from Bayer, Bristol-Myers Squibb, Boehringer Ingelheim, CVRx, Medtronic, Novartis, Pfizer, Sanofi und Servier. His research is supported by Deutsche Forschungsgemeinschaft (DFG), European Union and German Federal Ministry of Education and Research (BMBF). BHB received compensation from West Virginia University, Morgantown, WV, USA for her consultant work. MdZ, FG, KH, MH, MS, and RT report no competing interest.