Clinical Implementation and Evaluation for the Family-oriented Care CHIMPS-NET

NCT05106673 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 798

Last updated 2021-11-04

No results posted yet for this study

Summary

Despite the knowledge, that children of mentally ill parents are an important target group to be addressed by preventive and therapeutical interventions, there is often a lack of structured implementation of family-oriented interventions in clinical practice in Germany. Using a randomized controlled multicenter trial design with a large and wide-ranging sample (clinics for adult psychiatry and clinics for child and adolescent psychiatry, university clinics and clinics at the real health care) will examine changes in family-oriented practice and aspects of implementation to get a robust understanding of implementing family-oriented interventions in German clinical practice.

Conditions

  • Mental Health Issue

Interventions

BEHAVIORAL

Optimal pathways to care

The first implementation measure focuses on optimal ways of caring for mentally ill patients who are also parents with children living in the household. The main goals of this intervention are the specific information of the referring physician, the indicated referral of mentally ill parents and the consideration of underage children living in the household in the inpatient referral. The two main components are the evaluation of the attitudes of the medical and psychotherapeutic referrers towards the target group and the intervention as well as the development and implementation of an optimal care pathway. The optimization of the allocation is organized by Silke Pawils (University Medical Center Hamburg-Eppendorf).

BEHAVIORAL

Education and training program for the professionals

The second implementation intervention concerns the improvement of the professionals' attitudes, knowledge and skills. The two main components here being the assessment of the current state in all institutions within the clinical centers and the development and implementation of an education and training program. The employees of the randomized clinical centers in the intervention group will get a three-hour training. This intervention is organized by Svenja Taubner (University Hospital Heidelberg, Germany).

BEHAVIORAL

Systematic screening

The third implementation intervention includes a systematic screening process to improve detection of mentally ill parents with affected children. Employees of the clinical centers fill out two short questionnaires with the parents. This intervention project is organized by Sibylle M. Winter (Charité, Berlin, Germany).

OTHER

TAU

No Intervention: Treatment as usual These clinical centers will be the control group and will not get a specific implementation support during the implementation of CHIMPS.

Sponsors & Collaborators

  • Evangelisches Klinikum Bethel

    collaborator UNKNOWN
  • Charite University, Berlin, Germany

    collaborator OTHER
  • Universitätsklinikum Leipzig

    collaborator OTHER
  • University Hospital, Saarland

    collaborator OTHER
  • Immanuel Klinik Rüdersdorf

    collaborator UNKNOWN
  • LWL Klinik Gütersloh

    collaborator UNKNOWN
  • University Hospital, Aachen

    collaborator OTHER
  • University of Ulm

    collaborator OTHER
  • Universitätsklinikum Köln

    collaborator OTHER
  • University Hospital Freiburg

    collaborator OTHER
  • University Hospital Augsburg

    collaborator OTHER
  • University Medical Center Rostock

    collaborator OTHER
  • University Hospital Tuebingen

    collaborator OTHER
  • Helios Kliniken Schwerin

    collaborator OTHER
  • University of Magdeburg

    collaborator OTHER
  • Universitätsklinikum Koblenz - Landau

    collaborator UNKNOWN
  • HELIOS Hospital, Erfurt, Germany

    collaborator OTHER
  • Goethe University

    collaborator OTHER
  • Universitätsklinikum Hamburg-Eppendorf

    lead OTHER

Principal Investigators

  • Silke Wiegand-Grefe, Prof. Dr. · Universitätsklinikum Hamburg-Eppendorf

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-01
Primary Completion
2023-05-01
Completion
2023-09-01

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05106673 on ClinicalTrials.gov