Recalling and Anticipating Specific Positive Events to Boost Resilience in Adolescents (RASPERA)

July 6, 2023 updated by: Prof. dr. Filip Raes
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 Overview

Study Type

Interventional

Enrollment (Actual)

191

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Antwerpen, Belgium, 2020
        • Pius X - instituut
    • Limburg
      • Bilzen, Limburg, Belgium, 3740
        • Sint Lambertuscollege
      • Hasselt, Limburg, Belgium, 3500
        • GO! Next sportschool Hasselt
      • Hasselt, Limburg, Belgium, 3500
        • Scholen Kindsheid Jesu
    • Vlaams-Brabant
      • Kapelle-op-den-Bos, Vlaams-Brabant, Belgium, 1880
        • KOBOS Secundaire Scholen

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 16 years (Child)

Accepts Healthy Volunteers

No

Description

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:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group
Classes that will follow Positive Events Training.
PET is a group-based training program combining Memory Specificity Training (MEST; Raes, 2007) and Future Event Specificity Training (FEST; Dutch version of Hallford et al. (2020): Changing the Future: An initial test of Future Specificity Training). It comprises four sessions of 50 minutes each. The training is delivered in a standardized manner, using the Positive Event Training Manual developed for this study (content adapted from our MEST and FEST manuals). Following brief psychoeducation on the rationale, participants practice generating detailed specific memories and future events using neutral and positive cue-words. Participants are maximally supported and challenged by the trainer and by the other group-members to generate very specific and highly detailed memories and future events using mental imagery and drawing upon visual, olfactory, auditory and emotional elements of the events, including both contextual and sensory-perceptual details.
Active Comparator: Control group
Classes that will follow Bogus Control Training.
CREAT follows the exact same format and length as the PET training (i.e., delivered by a trainer in group over 4 x 50-minute sessions, including homework exercises). Following brief psychoeducation on the (bogus*) rationale behind PET, participants complete a series of creative writing exercises using funny and thought-provoking writing prompts. Just as in PET, participants are maximally supported and challenged by the trainer and by the other group-members, in this case to generate completions that are as creative and funny as possible. The investigators used CREAT successfully before in an online format as a bogus control training for a memory specificity training. (*) The investigators tell participants that these creative writing exercises have been found to be beneficial for mental wellbeing, as creative writing exercises cultivate creativity and stimulate participants' imagination skills.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
1 week before the intervention, 1 week after the intervention and 2 months after the intervention.
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.
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

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Positive affect
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Positive Affect subscale of the Positive and Negative Affect Schedule Scales (PANAS; Watson et al., 1988) to assess positive affect - The Positive Affect subscale of the PANAS consists of 10 items (words) that describe positive feelings (e.g., "excited"). Items are rated on a 5-point Likert scale going from 1 (very slightly or not at all) to 5 (extremely), where with higher scores reflecting higher positive affect.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Positive affect regulation
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Dampening and Savoring subscale of the Responses to Positive Affect scale, child version (RPA-C; Bijttebier et al., 2012) to assess positive affect regulation - The RPA-C consists of items reflecting both dampening items (e.g., "When you felt happy, how often did you think: "I don't deserve this"?") and savoring items responses (e.g., "When you felt happy, how often did you notice that you felt full of energy?"). All 17 items are rated on a 4-point Likert scale ranging from 1 (not at all) to 4 (very often).
One week before the intervention, one week after the intervention and two months after the intervention
Change in Anhedonia
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Leuven Anhedonia Self-report Scale (LASS, 2nd version; Nelis, Bastin, Raes, & Bijttebier 2018) to assess symptoms of anhedonia - The 12All 12 items (e.g., "There were few things I looked forward to.") are rated on a 5-point Likert scale going from 1 (completely untrue) to 5 (completely true) with higher scores reflecting higher levels of anhedonia.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Dampening
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Leuven Exeter Dampening Scale - General (LEDS, unpublished) to assess dampening.- The LEDS-G consists of 13 items (e.g., "I can only be happy if others are too.") that are rated on a 5-point Likert scale. Compared to the RPA dampening subscale, the LEDS-G aims to cover a larger variety of dampening appraisal styles.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Savoring
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Savouring Items for the Four-Factor Model of the Abridged Ways Of Savoring Checklist in Response to Everyday Events (Original scale Bryant and Vernoff, 2007; Four-Factor Model Chadwick, 2012) to assess savoring. - Items (e.g., "I looked for other people to share it with.") are rated on a 7-point Likert scale going from 1 (totally disagree) to 7 (totally agree), with higher scores reflecting higher levels of savoring.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Depressive symptoms and stress
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Depression, Anxiety, and Stress Scale (DASS-21; Lovibond & Lovibond, 1995) to assess basic mental health to control for baseline differences in the training groups, and to explore the generalised effect of PET on levels of depressive symptoms and stress at post-intervention and at follow-up. - The DASS-21 consists of 21 items (e.g., "I felt like my life had no meaning.") that are rated on a 4-point Likert scale going from 0 (never) to 3 (almost always).
One week before the intervention, one week after the intervention and two months after the intervention

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in episodic future thinking specificity (manipulation check)
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Episodic Future Thinking Test (EFT-T; Hallford et al., 2019) to assess episodic future thinking specificity. - Generated events will be coded as 0 or 1 (specific vs. non-specific) by the involved researchers.
One week before the intervention, one week after the intervention and two months after the intervention
Change in positive memory specificity (manipulation check)
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Autobiographical Memory Test (AMT, Raes et al., 2099) to assess positive memory specificity. - Generated memories will be coded as specific vs. non-specific (1 vs. 0) by the involved researchers.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Pleasure
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Two single-item ratings of the anticipated/anticipatory (future) or remembered/felt pleasure (past) associated with the events participants recall/generate on the AMT and EFT-T. - 1 (not at all applicable) to 9 (strongly applicable) response rating scale presented by each generated event.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Detail and mental imagery
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Two single-item ratings of level of detail and mental imagery associated with the events participants recall/generate on the AMT and EFT-T respectively. - 1 (not at all applicable) to 9 (strongly applicable) response rating scale presented by each generated event.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Perceived control and likelihood
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Two single-item ratings of perceived control and perceived likelihood of occurrence associated with the events participants generate on the EFT-test (no parallel items for the AMT). - 1 (not at all applicable) to 9 (strongly applicable) response rating scale presented by each generated event.
One week before the intervention, one week after the intervention and two months after the intervention
Change in Positive feelings
Time Frame: One week before the intervention, one week after the intervention and two months after the intervention
Two additional single-items ratings of anticipated/anticipatory (future) or remembered/felt positive feelings in general (past) associated with the events participants recall/generate on the AMT and EFT-T. - 1 (not at all applicable) to 9 (strongly applicable) response rating scale presented by each generated event.
One week before the intervention, one week after the intervention and two months after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Filip Raes, Prof. dr., KU Leuven

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 21, 2022

Primary Completion (Actual)

May 13, 2023

Study Completion (Actual)

May 13, 2023

Study Registration Dates

First Submitted

February 14, 2023

First Submitted That Met QC Criteria

February 23, 2023

First Posted (Actual)

March 7, 2023

Study Record Updates

Last Update Posted (Actual)

July 7, 2023

Last Update Submitted That Met QC Criteria

July 6, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • G049019N (Research Foundation - Flanders)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The coded, pseudonomized dataset will be uploaded in a csv format to OSF (in a restricted access repository).

IPD Sharing Time Frame

The coded, pseudonomized dataset will be uploaded in a csv format to OSF (in a restricted access repository) upon publication of the research results.

IPD Sharing Access Criteria

Coded, pseudonomized data can be shared with regulatory authorities, ethical committees, other parties that collaborate with the research team. Other researchers will only have access to the coded, pseudonomized data, and only if they agree with the confidentiality rules agreed upon within this study.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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