Impact of Preventive Mental Health Programme on Social/Emotional Functioning and Resilience in Children in South Africa

NCT06445777 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-10-15

No results posted yet for this study

Summary

The goal of this clinical trial is to test the effectiveness of a mental health prevention and promotion programme delivered to children (ages 8 to 13) living in under-resourced communities in South Africa.

The main question it aims to answer is:

Does the programme increase resilience and improve psychological well-being?

Participants will be asked to attend the programme twice a week after school for a period of six weeks and complete a series of questionnaires.

Researchers will compare children who attended the programme to those who did not to see if the programme resulted in better social/emotional functioning and resilience.

Conditions

  • Psychological Well-Being

Interventions

BEHAVIORAL

Mental Health Prevention and Promotion

The Inner Lion Programme is made up of 12 interactive workshops which are based on four key pillars: building confidence by identifying strengths and personal qualities; improving emotional intelligence and self-awareness; establishing adaptive coping strategies and channels of support; and boosting resilience. Professionally created by Child Psychologist Stijn de Leeuw together with an advisory team of psychologists from the Netherlands and South Africa, the programme follows a carefully structured and curated prevention and promotion mental health curriculum with games, crafting activities, psycho-educational stories, dance, movement, and breathing exercises. Workshops are led by local role models (a male-female duo) with lived experience trained to be mental health coaches.

Sponsors & Collaborators

  • University of Cape Town

    collaborator OTHER
  • King's College London

    collaborator OTHER
  • Little Lions Child Coaching

    lead OTHER

Principal Investigators

  • Susan Malcolm-Smith · University of Cape Town

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
8 Years
Max Age
13 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-08-19
Primary Completion
2024-12-10
Completion
2025-03-31

Countries

  • South Africa

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06445777 on ClinicalTrials.gov