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Resilience for Children and Young People in Foster Care and Residential Care in Denmark

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02220179
Recruitment Status : Unknown
Verified June 2015 by Poul Bak, University of Aarhus.
Recruitment status was:  Active, not recruiting
First Posted : August 19, 2014
Last Update Posted : June 2, 2015
Sponsor:
Collaborator:
TRYG Foundation
Information provided by (Responsible Party):
Poul Bak, University of Aarhus

Brief Summary:
In this project we invite 9.000 children and young persons in Denmark and their foster parents and staff at the residential institutions to participate in a cluster randomized controlled intervention study where we aim to test the effectiveness of a web based knowledge and inspiration program about resilience for children, adolescents and adults (called myresilience.org). The complete CONSORT trial protocol is available at http://myresilience.org/ at the subsite 'about us'.

Condition or disease Intervention/treatment Phase
Children and Adolescents in Foster Care and Residential Care Behavioral: The Resilience Program Not Applicable

Detailed Description:
The complete CONSORT trial protocol is available at http://myresilience.org/ at the subsite 'about us'.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 9000 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose: Health Services Research
Official Title: Resilience for Children and Young People
Study Start Date : August 2014
Estimated Primary Completion Date : August 2017
Estimated Study Completion Date : August 2017

Arm Intervention/treatment
No Intervention: control
service as usual
Experimental: Intervention group 1
Participants are offered access to the web based resilience program
Behavioral: The Resilience Program
Se the CONSORT trial protocol at http://myresilience.org/ at the subsite 'about us'

Experimental: Intervention group 2
Participants are offered access to the web based resilience program and are also invited to join a short introduction course about the program
Behavioral: The Resilience Program
Se the CONSORT trial protocol at http://myresilience.org/ at the subsite 'about us'




Primary Outcome Measures :
  1. National Test in Danish Reading [ Time Frame: Outcome data will be collected on the average 2 years after intervention ]
    The National test in danish reading is a standard performance test which is mandatory for all danish student. It is administered for every other year.


Secondary Outcome Measures :
  1. The frequency of Care collapse [ Time Frame: Outcome data will be collected on the average 2 years after intervention ]
    All incidents of collapse in a care relation is registered by the danish authorities. The informations in this register are used for this outcome measure.


Other Outcome Measures:
  1. Questionnaire data [ Time Frame: data collected august 2015 ]
    Se the trial CONSORT protocol at http://myresilience.org/ at the subsite 'about us'



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   up to 23 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • All children and adolescents registered in foster care in Denmark on august 11th 2014.
  • All children and adolescents registered in residential care in Denmark on august 11th 2014.

Exclusion Criteria:

• Request for legal protection against contacts from researchers.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02220179


Locations
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Denmark
Aarhus University
Aarhus, Denmark, 8000
Sponsors and Collaborators
Poul Bak
TRYG Foundation
Investigators
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Principal Investigator: Poul L Bak, MD University of Aarhus
Additional Information:
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Responsible Party: Poul Bak, MD, University of Aarhus
ClinicalTrials.gov Identifier: NCT02220179    
Other Study ID Numbers: DK-res-care
First Posted: August 19, 2014    Key Record Dates
Last Update Posted: June 2, 2015
Last Verified: June 2015