Hautmann, Christopher http://orcid.org/0000-0001-5155-3762
Rausch, Jana http://orcid.org/0000-0002-8063-0998
Geldermann, Nina
Oswald, Felix http://orcid.org/0000-0003-1270-8885
Gehlen, Danny http://orcid.org/0000-0001-7316-6157
Hellmich, Martin http://orcid.org/0000-0001-5174-928X
Rosenberger, Kerstin Daniela http://orcid.org/0000-0003-3459-3812
Samel, Christina
Woitecki, Katrin
Walter, Daniel http://orcid.org/0000-0002-2430-7117
Adam, Julia http://orcid.org/0000-0002-7469-5461
Dachs, Lydia
Goletz, Hildegard
Halder, Joya
Kinnen, Claudia
Mücke, Kristina
Otte, Janina
Perri, Daniela
Rademacher, Christiane
Schürmann, Stephanie
Viefhaus, Paula http://orcid.org/0000-0003-4929-8138
Wolff Metternich-Kaizman, Tanja
Döpfner, Manfred
Funding for this research was provided by:
Innovation Committee at the Federal Joint Committee (01VSF18027)
Universitätsklinikum Köln
Article History
Received: 13 September 2021
Accepted: 28 September 2021
First Online: 15 October 2021
Declarations
:
: The ethical standards of the study are based on the Declaration of Helsinki [CitationRef removed], the code of conduct of the Federal Chamber of Psychotherapists in Germany (BPtK) [CitationRef removed], and the North Rhine-Westphalia Data Protection Act (DSG NRW) [CitationRef removed]. The study-specific risks are considered no higher than those found in routine care. Other interventions deemed necessary will not be prevented by the study. The trial protocol has been approved by the Ethic Commission of the Medical Faculty of the University of Cologne (ID 18–435). Changes to the trial protocol or complications during the trial will be reported to the ethics committee. If these changes are considered to be of relevance to the participants of the study, they will also be informed. The trial will be stopped if the risk-benefit ratio has to be revised.All study participants (therapists, caregivers, children) will receive information sheets and will be informed by the project staff about the purpose of the study and its procedure as well as the way data is collected, stored, and processed. Therapists and both caregivers have to give their written informed consent to participate in the study. For children, it is required that they submit a declaration of intent. Teachers also provide questionnaire data at the study assessments. However, because all information is gathered as part of the routine care, a separate informed consent is not considered necessary.
: Not applicable.
: CH has received a research grant from the Innovation Committee to conduct the study. MD, KW, DW, JA, LD, HG, JH, CK, DP, CR, SS, and TWMK receive royalties from publishing companies (e.g., Hogrefe, Beltz) for the rating scales or treatment manuals which are used in this study. MD, KW, DW, LD, HG, CK, CR, SS, and TWMK also receive fees for supervising therapists of this study. JR, NG, FO, DG, MH, KDR, CS, KM, JO, and PV all declare that they are not aware of any conflicts of interests.