- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06856408
Power of Growth - Digitally Assisted Intervention for the Early Childhood Educators' Self-efficacy Teamwork and Children's Behavioral Challenges. (FinnPoG)
Power of Growth RCT Study
This is an RCT study investigating the efficacy of digital intervention focusing on enhancing positive directing skills for teams of early childhood education (ECE) professionals. The aims are to study 1) changes in the ECEs' self-assessed self-efficacy experience in the intervention group compared to the control group; 2) changes in the behavioral challenges of the children in the ECEs' groups assessed by the parents in the intervention group compared to the control group; and 3) changes in the ECEs' guidance methods in the intervention group compared to the control group. We will also study changes in the wellbeing of ECEs and teamwork in both treatment groups. The sample size will consist of approximately 64 teams of ECEs. Hence, altogether there will be approximately 200 study subjects.
The intervention is aimed at ECE teams and its goal is to strengthen and unify the team positive guidance practices in children's groups. The intervention includes self-learning material and teams online coaching in which the entire team participates simultaneously. The self-material includes 360 videos of everyday situations in the daycare and videos can be watched with VR glasses. The participants practice the skills systematically with their group of children. The duration of the intervention is approximately 12 weeks and team coaching are carried out approximately every two weeks.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Katja Toivonen, Master of Education
- Phone Number: +358408203195
- Email: katja.toivonen@utu.fi
Study Locations
-
-
Select
-
Municipalities, Select, Finland, 20660
- Recruiting
- Early Childhood Education
-
Contact:
- Katja Toivonen, Master of Education
- Phone Number: +358 50 469 8681
- Email: katja.toivonen@utu.fi
-
Turku, Select, Finland, 20660
- Recruiting
- Research Centre of Child Psychiatry
-
Contact:
- Katja Johanna Toivonen, Master of Education
- Phone Number: +35850 469 8681
- Email: katja.toivonen@utu.fi
-
Contact:
- Laura Kortesoja, Master of Education
- Phone Number: +358 50 477 1437
- Email: laura.kortesoja@utu.fi
-
Contact:
- Andre Sourander, MD Professor
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Participant is working in a daycare centre team that is participating to the study. Sufficient knowledge in Finnish language.
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Digitally assisted intervention including online coaching
The intervention is a structured remote coaching concept for professionals working in early childhood education.
The intervention will use virtual reality glasses and 360° video material.
The intervention consists of six self-study themes about positive pedagogy and team work.
The themes will be combined with remote coaching for the team (3-5 people) and the skills will be practiced with their own group of children.
The intervention length is 2-3 months.
There will approximately 34 teams in intervention and control groups.
|
The aim of the study is to find out how intervention affects the early childhood educators' self-efficacy teamwork and the changes in children's behavioral challenges.
This RCT study has two parallel groups where teams of the daycare centres are randomized to intervention or control group.
The research data is collected using electronic surveys and interviews.
|
|
No Intervention: Control
No digital assisted intervention or online coaching.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ECE Teacher Self Efficacy
Time Frame: From baseline to 3, 6 months after randomisation
|
TEIP (Teacher Efficacy for Inclusive Practices)
|
From baseline to 3, 6 months after randomisation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceptions of Team work
Time Frame: From baseline to 3, 6 months after randomisation
|
TeamSTEPPS
|
From baseline to 3, 6 months after randomisation
|
|
Behaviour problems of the child
Time Frame: From baseline to 3, 6 months after randomisation
|
Parent evaluates (SDQ, ARI, ICU)
|
From baseline to 3, 6 months after randomisation
|
|
Burn out
Time Frame: From baseline to 3, 6 months after randomisation
|
BBI -15 (Bergen burnout inventory)
|
From baseline to 3, 6 months after randomisation
|
|
Confidence in ability to deal with child´s challenging behavior
Time Frame: From baseline to 3, 6 months after randomisation
|
Questions about professional´s perceived confidence in ability to deal with child´s challenging behavior
|
From baseline to 3, 6 months after randomisation
|
|
Work satisfaction
Time Frame: From baseline to 3, 6 months after randomisation
|
Questions about perceived work satisfaction
|
From baseline to 3, 6 months after randomisation
|
|
Perceived skills
Time Frame: From baseline to 3, 6 months after randomisation
|
Questions about the content and themes of the intervention
|
From baseline to 3, 6 months after randomisation
|
|
Questionnaire on interaction skills: attuned interaction and guidance
Time Frame: From baseline to 3, 6 months after randomisation
|
Questions about interaction skills
|
From baseline to 3, 6 months after randomisation
|
|
The workload of guiding the child group
Time Frame: From baseline to 3, 6 months after randomisation
|
Questions about professional´s perceived workload of guiding the child group.
|
From baseline to 3, 6 months after randomisation
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PoG-001
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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