Yhteispeli - Effectiveness Study on Promoting Childrens' Socio-emotional Skills in School

Sponsor
Finnish Institute for Health and Welfare (Other)
Overall Status
Completed
CT.gov ID
NCT02178332
Collaborator
Tampere University (Other)
4,400
1
2
31
142

Study Details

Study Description

Brief Summary

The purpose of this cluster randomised trial is to investigate whether the Yhteispeli whole school programme is effective in improving children's socio-emotional skills and mental health and socio-emotional skills.

All Finnish elementary schools and their classes in 1-3 grades were invited to participate in the study. The schools were randomly allocated to receive either Yhteispeli programme or two lectures

Condition or Disease Intervention/Treatment Phase
  • Other: Yhteispeli, whole school programme
  • Other: Two theoretical lectures
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
4400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Yhteispeli: Intervention Effectiveness on Elementary School Childrens' Socio-emotional Skills and Psychiatric Symptoms
Study Start Date :
Mar 1, 2013
Actual Primary Completion Date :
Sep 30, 2015
Actual Study Completion Date :
Sep 30, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Yhteispeli, whole school programme

Yhteispeli-programme aims to support children's socio-emotional skills and well being at schools. Schools receive the Yhteispeli manual and teachers receive 3 and head masters 2 lecture days about use of Yhteispeli methods including group discussions and exercises. In addition every school is visited 4 times to support the use of Yhteispeli methods. (Lectures for the head masters March 2013 - November 2013, teachers August 2013 - January 2014)

Other: Yhteispeli, whole school programme

Active Comparator: Two theoretical lectures

Teachers receive two theoretical lectures on development of children's socio-emotional skills (3 hours in November 2013 and 3 hours in March 2014 ).

Other: Two theoretical lectures

Outcome Measures

Primary Outcome Measures

  1. Change in children's psychiatric symptoms [6 months after baseline and 18 months after baseline]

    SDQ - The Strengths and Difficulties Questionnaires

  2. Change in children's socio-emotional skills [6 months after baseline and 18 months after baseline]

    A set of socio-emotional skills tests A set of questions regarding bullying

Secondary Outcome Measures

  1. Change in children's emotion recognition (and processing) [6 months after baseline and 18 months after baseline]

    A set of emotion recognition (and processing) tests

  2. Change in children's executive functions [6 months after baseline and 18 months after baseline]

    A set of cognitive functions tests

  3. Change in teacher and work community (occupational) wellbeing [6 months after baseline and 18 months after baseline]

    A set of teacher's occupational and work community wellbeing tests

Other Outcome Measures

  1. Change in teacher and parent interaction [6 months after baseline and 18 months after baseline]

    A set of teacher-parent interaction tests

  2. Change in children's and teachers' perceptions of class environment [6 months after baseline and 18 months after baseline]

    A set of class environment questions rated by the teacher and children

  3. Change in teaching and parenting styles [6 months after baseline and 18 months after baseline]

    A set of questions regarding child rearing

  4. Change in teachers' and parents' socio-emotional skills [6 months after baseline and 18 months after baseline]

    A set of questions regarding adult socio-emotional skills

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • All children from volunteering elementary schools and classes (grades 1 to 3) whose parents gave consent to participate
Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Olli Kiviruusu Helsinki Finland

Sponsors and Collaborators

  • Finnish Institute for Health and Welfare
  • Tampere University

Investigators

  • Principal Investigator: Olli Kiviruusu, PhD, Finnish Institute for Health and Welfare

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Olli Kiviruusu, Research Manager, Finnish Institute for Health and Welfare
ClinicalTrials.gov Identifier:
NCT02178332
Other Study ID Numbers:
  • THL/455/6.00.00/2014
First Posted:
Jun 30, 2014
Last Update Posted:
Dec 13, 2021
Last Verified:
Nov 1, 2021

Study Results

No Results Posted as of Dec 13, 2021