CClinicalTrials.gg
Status unknownNCT02220179Updated Jun 2, 2015

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

An interventional study of The Resilience Program in Children and Adolescents in Foster Care and Residential Care, sponsored by Poul Bak. Status unknown at 1 site in Denmark. Open to participants aged Up to 23 Years. Per ClinicalTrials.gov, last updated 2015-06-02.

Sponsored by Poul Bak · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Jun 2015), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
9,000
Allocation
Randomized
Ages
Up to 23 Years
Sex
All
01

Study 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'.

Read the detailed description

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

02

Conditions studied

  • Children and Adolescents in Foster Care and Residential Care
03

In context

Lead sponsor

This is the only study on the registry with Poul Bak as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 23 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

Exclusion Criteria:

  • Request for legal protection against contacts from researchers.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
9,000 participants (estimated)

Study arms

  • No intervention
    control

    service as usual

  • Experimental
    Intervention group 1

    Participants are offered access to the web based resilience program

    Behavioral: The Resilience Program

  • 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

Interventions

  • BehavioralThe Resilience Program

    Se the CONSORT trial protocol at http://myresilience.org/ at the subsite 'about us'

06

What researchers measure

Primary outcomes

  1. National Test in Danish Reading

    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.

    Time frame: Outcome data will be collected on the average 2 years after intervention

Secondary outcomes

  1. The frequency of Care collapse

    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.

    Time frame: Outcome data will be collected on the average 2 years after intervention

Other outcomes

  1. Questionnaire data

    Se the trial CONSORT protocol at http://myresilience.org/ at the subsite 'about us'

    Time frame: data collected august 2015

07

Study locations

1 site
  • Aarhus University
    Aarhus, 8000, Denmark
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02220179
Lead sponsor
Poul Bak
Collaborators
TRYG Foundation
Responsible party
Poul Bak (MD, University of Aarhus) — Sponsor-investigator
First posted
Aug 19, 2014
Start date
Aug 2014
Primary completion
Aug 2017 (estimated)
Completion
Aug 2017 (estimated)
Last update
Jun 2, 2015

Study contacts

Poul L Bak, MD
principal investigator · University of Aarhus

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2015. You cannot join it, but the record below documents what was studied.

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