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Clinical Trials/NCT05757180
NCT05757180CompletedNot Applicable

Recalling and Anticipating Specific Positive Events to Boost Resilience in Adolescents

Prof. dr. Filip Raes5 sites in 1 country191 target enrollmentStarted: October 21, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
191
Locations
5
Primary Endpoint
Change in Mental wellbeing

Study Overview

Brief Summary

Many young people are experiencing stress-related mental health problems, with some recent studies suggesting this number is increasing. Especially now, in the context of the COVID-19 pandemic, there is a significant increase in depression and anxiety in adolescents. An important way to help address this challenge is not so much to focus on trying to repair what makes young people vulnerable but to focus on building resilience. Resilience refers to the ability to successfully deal with stressful experiences. Recent research shows that being able to vividly remember and imagine positive events can buffer the negative consequences of stress, and makes a convincing case that training adolescents in recalling and anticipating positive events would promote resilience and thereby improve their mental wellbeing. And this is exactly what the current project sets out to do for the very first time. Adolescents will receive a playful group-training in school to make them better at recalling and anticipating positive events, which is expected to help them to bounce back more swiftly from challenging or otherwise stressful life events. The investigators predict that youngsters who follow our Positive Event Training will experience more positive emotions, will show improved resilience and report better mental wellbeing. The investigators will also develop a free online training protocol for teachers so that schools can provide this resilience program on their own, without the need of external professional trainers.

Study Design

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

Eligibility Criteria

Ages
12 Years to 16 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All adolescents of the selected classes of the participating schools (12-16 years; 1st and 2nd grade of secondary school) who want to take part in the study and give informed consent (own informed consent and active parental informed consent) will be allowed to take part in the study.
  • To minimize the risk of too much heterogeneity in our final sample, for instance due to context factors related to the type of education, the investigators will first recruit classes of adolescents that follow general secondary education. Future studies (after PET has been properly evaluated in this study) should also be conducted in samples of adolescents following other types of secondary education.

Exclusion Criteria

  • Not provided

Arms & Interventions

Intervention group

Experimental

Classes that will follow Positive Events Training.

Intervention: Positive Events Training (PET) (Behavioral)

Control group

Active Comparator

Classes that will follow Bogus Control Training.

Intervention: CREAtive writing Training (CREAT) (Behavioral)

Outcomes

Primary Outcomes

Change in Mental wellbeing

Time Frame: One week before the intervention, one week after the intervention and two months after the intervention; The SWEMWBS consists of seven statements (e.g., "I felt relaxed.") about thoughts and feelings that are scored on a 5-point Likert scale ranging from

Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS; Stewart-Brown et al., 2009) to assess mental wellbeing - The SWEMWBS consists of seven statements (e.g., "I felt relaxed.") about thoughts and feelings that are scored on a 5-point Likert scale ranging from 1 (never) to 5 (always). Higher scores reflect higher mental wellbeing.

Change in Resilience

Time Frame: 1 week before the intervention, 1 week after the intervention and 2 months after the intervention.

Connor-Davidson Resilience Scale (CD-RISC, short version) to assess resilience - This scale consists of 10 items (e.g., "Dealing with stress makes me stronger.") that are rated on a 5-point Likert scale going from 1 (not at all) to 5 (very often), with higher scores indicating higher resilience.

Secondary Outcomes

  • Change in Dampening(One week before the intervention, one week after the intervention and two months after the intervention)
  • Change in Savoring(One week before the intervention, one week after the intervention and two months after the intervention)
  • Change in Positive affect(One week before the intervention, one week after the intervention and two months after the intervention)
  • Change in Positive affect regulation(One week before the intervention, one week after the intervention and two months after the intervention)
  • Change in Depressive symptoms and stress(One week before the intervention, one week after the intervention and two months after the intervention)
  • Change in Anhedonia(One week before the intervention, one week after the intervention and two months after the intervention)

Investigators

Sponsor
Prof. dr. Filip Raes
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Prof. dr. Filip Raes

Professor

KU Leuven

Study Sites (5)

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