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Evaluation of the Effectiveness of a School-based Intervention to Improve the Wellbeing of Children Aged 8-11 Years.

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University College Dublin

Status

Enrolling

Conditions

Child, Only
Well-Being, Psychological

Treatments

Behavioral: A Lust for Life
Behavioral: Waiting List Control

Study type

Interventional

Funder types

Other

Identifiers

NCT06135779
HS-22-80-Carr

Details and patient eligibility

About

The aim of this study is to evaluate the effectiveness of a universal school-based intervention, which aims to improve the wellbeing of children aged 8 to 11 years, who are attending 3rd class or 4th class in primary level education in Ireland.

Full description

An estimated 10-20% of children and adolescents worldwide experience mental health difficulties, with 50% of difficulties emerging before the age of 14 years. School is an influential environment for young people, with school-based interventions consistently delivering positive mental health and wellbeing programmes in a cost-effective manner.

A Lust for Life (ALFL) is a universal teacher-led programme which aims to build resilience, increase wellbeing, and enhance emotional literacy of 8-13 year old school children. The programme spans ten 40-minute classes. The ALFL curriculum draws on multiple sources including contemporary positive psychology; traditional, second, and third wave cognitive behaviour therapy (CBT); and developmental, educational, and health psychology. In ALFL children learn the following specific self-regulation skills: naming and rating the intensity of emotions; linking thoughts, feelings and actions; mindfulness; breathing exercises; visualization exercises; progressive muscle relaxation; positive self-talk (gratitude, optimism, and cognitive restructuring); obtaining social support from adults and peers; assertiveness; managing bullying; and using the internet safely. Skills are learned through didactic instruction, video modelling, in-class experiential exercises, and homework practice. The ongoing development of the ALFL programme follows best practice, with the most recently refined programme evaluated in this study.

This quasi-experimental randomized controlled trial study involves an experimental group and a waiting list control group of children aged between 8-11 years. All study participants will complete the Feeling Better Scale, Stirling Children's Wellbeing Scale, and Revised Children's Anxiety and Depression Scale at pre-intervention. Participants will complete the questionnaires online. Following this, schools randomly assigned to the experimental group will receive the ALFL programme, while those randomly assigned to the control group will be placed on a 12-week waiting list and receive curriculum as usual. At post-intervention, the questionnaire measures will be completed online by all study participants. The participants in the experimental group will also complete a brief Satisfaction Scale. The waiting list control group will then receive the A Lust for Life programme.

Enrollment

300 estimated patients

Sex

All

Ages

8 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children aged 8-11 years
  • Enrolled in 3rd and 4th classes in Primary School in Ireland
  • Obtain written informed consent from parents/guardians
  • Provide written assent

Exclusion criteria

  • Failure to meet inclusion criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

A Lust for Life programme group
Experimental group
Description:
A Lust for Life programme will be delivered to participants by their class teachers in ten weekly sessions
Treatment:
Behavioral: A Lust for Life
Waiting list control group
Other group
Description:
Participants will receive curriculum as usual from their class teacher, and placed on a 12-week waiting list for the programme.
Treatment:
Behavioral: Waiting List Control

Trial contacts and locations

1

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Central trial contact

Alan Carr, Professor

Data sourced from clinicaltrials.gov

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