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Clinical Trials/NCT05061381
NCT05061381UnknownNot Applicable

Evaluating the Impact of a School Wellbeing Programme on Internalising Problems in Primary School Children

University College Dublin2 sites in 1 country400 target enrollmentStarted: October 11, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
400
Locations
2
Primary Endpoint
Symptoms of anxiety and low mood measured by the Revised Children's Anxiety and Depression Scale Short Form

Study Overview

Brief Summary

The aim of this study is to assess the effectiveness of a school-based multi-component universal programme for the reduction of internalising problems (i.e. anxiety and low mood) in primary school pupils.

Detailed Description

Childhood and adolescence are important developmental phases for wellbeing and mental health. School has been noted in psychological literature to be a favourable environment for mental health initiatives, such as school-based programmes. Universal programmes are programmes delivered to all pupils irrespective of perceived need and have several advantages, including having a wide reach, avoiding the need for screening and are less stigmatising.

A Lust for Life is a universal school-based multi-component intervention whose target is to build well-being and emotional resilience in children. The programme was informed by evidence-based psychological approaches including cognitive behaviour therapy, positive psychology and mindfulness and consists of six lessons, each delivered by the pupils' school teacher on a weekly basis. The lessons involve classroom discussions, videos, classroom activities and homework assignments.

Study participants will complete the Revised Children's Anxiety and Depression Scale Short Format, Coping strategy indicator and Self-Efficacy Questionnaire for Children pre-intervention. Following this, schools randomly assigned to the experimental group will receive A Lust for Life, while those randomly assigned to the control group will be placed on a sixteen-week waiting list. The questionnaire measures and a Brief Satisfaction Scale will be completed by participants at post-intervention. In addition, a six-week follow-up assessment will determine whether the effects of the programme are sustained over a period of time. The programme will be delivered in the waiting list control group schools after the six-week follow-up assessment.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
10 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Enrolled in primary school in Ireland
  • Obtain written informed consent from parents/guardians
  • Provide written assent

Exclusion Criteria

  • Failure to meet inclusion criteria

Outcomes

Primary Outcomes

Symptoms of anxiety and low mood measured by the Revised Children's Anxiety and Depression Scale Short Form

Time Frame: 16 weeks

25-item self-report measure of anxiety and depression symptoms of individuals aged 8-18 years.

Secondary Outcomes

  • Coping skills as measured by the Coping Strategy Indicator(16 weeks)
  • Self-efficacy as measured by the Self-Efficacy Questionnaire for Children(16 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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