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CompletedNCT04509531ResilienceUpdated Sep 28, 2021

Building Resilience in Cyberbullying Victims

An interventional study of Wise Intervention (SA, ITP and resilience) and Standard preventive intervention in Cyberbullying, Depression and Non Suicidal Self Injury, sponsored by University of Deusto. Completed at 1 site in Spain. Open to participants aged 11 Years to 19 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-09-28.

Sponsored by University of Deusto · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
850
Allocation
Randomized
Ages
11 Years to 19 Years
Sex
All
01

Study summary

This study evaluates the effectiveness of a wise intervention based on self-affirmation (SA) and Implicit Theories of Personality (ITP) building resilience in victims. Half of the participants will receive the experimental intervention, while the other half will receive a control intervention.

Read the detailed description

Bullying victimization can harm victims' mental health. Numerous studies have shown that, when an adolescent is a victim of cyberbullying, the risk of developing numerous mental health problems increases. Tackling the problem of cyberbullying victims' worsening mental health involves at least (1) reducing bullying itself, as this would reduce the prevalence of victimization, and (2) building resilience in the victims so that their mental health does not worsen. In recent years, a number of preventive interventions have been developed aimed at reducing cyberbullying but not so much focused on building resilience in the victims. Very recently, interest in scientific social psychology has grown due to a new approach to interventions, which have been called "wise interventions." This approach involves a set of rigorous techniques, based on theory and research, that address specific psychological processes to help people thrive in various life environments. The main objective of this project is to extend the previous findings to the mental health effects of online victimization in adolescents. In this project it will be designed and evaluated the effectiveness of an wise intervention aimed at (1) reducing online bullying, as this would reduce the prevalence of victimization; and (2) building resilience in victims so that the negative impact of victimization on their mental health will be reduced. The secondary objective will be to evaluate the moderating role of gender and the degree of development in the effects of the intervention.The study will involve the evaluation of the intervention in a sample of around 600 adolescents randomly allocated to experimental and control condition.

02

Conditions studied

  • Cyberbullying
  • Depression
  • Non Suicidal Self Injury
  • Social Anxiety
  • Eating Disorders

Keywords

  • Adolescence
  • Prevention
  • Cyberbullying
  • Depression
  • Non Suicidal Self Injury
  • Social Anxiety
  • Eating Disorders
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,643 are open to participants now.

This study's enrollment of 850 is above the median of 84 across 6,718 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

University of Deusto is the lead sponsor of 20 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
11 Years to 19 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Spanish or Basque understanding
  • Permission by parents
  • Voluntarity

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
850 participants (actual)

Study arms

  • Experimental
    Experimental: SA, ITP and Resilience

    1 hour Wise intervention (based on SA, ITP and resilience) consisting on several tasks to be completed online individually.

    Behavioral: Wise Intervention (SA, ITP and resilience)

  • Other
    Standard preventive intervention

    1 hour educational intervention (about internet risks such as sexting and grooming) consisting on several tasks to be completed online individually.

    Behavioral: Standard preventive intervention

Interventions

  • BehavioralWise Intervention (SA, ITP and resilience)

    The intervention will be based on four general types of change strategies: (1) scientific knowledge, (2) generation of new meanings, (3) commitment through action, and (4) active reflection. This will include activities such as reading scientific information about social behavior and its role in people's well-being and mental health, the meaning of online victimization experiences and ways to react to them, experiences of other young people of their age, and self-persuasion exercises that involve an active commitment to change. Furthermore, it provides a number of strategies to manage everyday conflicts among adolescents. This intervention teaches them new ways to manage these difficulties through different actions (relaxation, distraction, sports, etc.). Finally, they are asked to plan the strategies they will use in the future in the face of some difficulties and to recommend some guidelines for another adolescent who may be going through a similar situation.

  • BehavioralStandard preventive intervention

    The control intervention will involve scientific information and education about internet risks such as sexting and grooming.

06

What researchers measure

Primary outcomes

  1. Change from baseline scores of the Cyber Bullying Questionnaire (CBQ; Calvete et al., 2010; Gámez-Guadix, Villa-George, & Calvete, 2014)

    Self reported levels of perpetration (9 items) and victimization (9 items) of peer cyber aggression. Each item is scored 0-4 (0 = never; 4 = almost every week).

    Time frame: Baseline, 3 months, and 6 months.

  2. Change from baseline scores of the Functional Assessment of Self-Mutilation (FASM; Lloyd, Kelley & Hope, 1997)

    Self reported levels of Non-Suicidal Self-Harm (NSSH). The 6 most representative items will be used. Each item is scored 0-4 (0 = 0 times; 4 = \> 11 times).

    Time frame: Baseline, 3 months, and 6 months.

  3. Change from baseline scores of the reduced version of the Center for Epidemiological Studies Depression (CES-D; Rueda-Jaimes et al., 2009).

    Self reported symptoms of depression through 10 items, with a four-point response scale ranging from 0 (practically never) to 3 (almost all the time).

    Time frame: Baseline, 3 months, and 6 months.

  4. Change from baseline scores of the reduced Spanish version of the Social Anxiety Scale for Adolescents (SAS-A; La Greca & Lopez, 1998; Nelemans et al., 2019)

    Self reported symptomatology of social anxiety through 12 items, with a five-point response scale ranging from 1 (not at all) to 5 (all the time).

    Time frame: Baseline, 3 months, and 6 months.

  5. Change from baseline scores of the reduced version of the Eating Attitudes Test (EAT; Garner & Garfinkel, 1979; EAT-8, Richter, Strauss, Braehler, Altmann & Berger, 2016)

    Self reported symptomatology associated with eating disorders through 8 items, with a six-point response scale ranging from 1 (never) to 6 (always).

    Time frame: Baseline, 3 months, and 6 months.

Secondary outcomes

  1. Change from baseline scores of Entity and incremental theories (Levy, Stroessner, & Dweck, 1998).

    Entity and incremental theories will be evaluated using eight items adapted to the situations of bullying in schools. Items are rated on a six-point scale ranging from 1 (strongly disagree) to 6 (strongly agree).

    Time frame: Baseline, 1 hour, 3 months, and 6 months.

  2. Change from baseline scores of attitude towards cyberbullying measure

    Self reported ad hoc measures developed by the research team of the attitude towards cyberbullying. The participants will classify one situation of cyberbullying through adjectives using the semantic differential technique with a response range of 7 points.

    Time frame: Baseline, 1 hour, 3 months, and 6 months.

  3. Change from baseline scores of attitude towards different courses of action measure

    Self reported ad hoc measures developed by the research team of the attitude towards different courses of action when the adolescent witnesses cyberbullying. The participants will rate four different ways to react to cyberbullying through semantic differential items.

    Time frame: Baseline, 1 hour, 3 months, and 6 months.

  4. Change from baseline scores of the anticipation of reactions and behaviors measure

    Self reported ad hoc measures developed by the research team of the anticipation of reactions and behaviors when the adolescent is a witness. The participants will answer seven items on a five-point response scale ranging from 0 (totally disagree) to 3 (totally agree).

    Time frame: Baseline, 1 hour, 3 months, and 6 months.

  5. Change from baseline scores of the intention to use different strategies when the adolescent is exposed to diverse stressors

    Self reported ad hoc measures developed by the research team of the intention to use different strategies when the adolescent is exposed to diverse stressors, participants will complete six items on a four-point response scale ranging from 0 (never or almost never) to 3 (always or almost always).

    Time frame: Baseline, 1 hour, 3 months, and 6 months.

07

Study locations

1 site
  • University of Deusto
    Bilbao, Bizkaia 48080, Spain
08

References and documents

Study documents

  • Protocol and statistical analysis plan · May 31, 2020
  • Informed consent form · May 31, 2020

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — Raw data will be available at OSF when the results of the study are published.

Supporting information: Study protocol, Sap, Icf

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04509531
Lead sponsor
University of Deusto
Collaborators
Fundación Alicia Koplowitz
Responsible party
Esther Calvete (Principal Investigator, Deusto Stress Research Team, University of Deusto, University of Deusto) — Principal investigator
First posted
Aug 12, 2020
Start date
Sep 15, 2020
Primary completion
Jul 31, 2021
Completion
Jul 31, 2021
Last update
Sep 28, 2021

Study contacts

Esther Calvete, PhD
principal investigator · University of Deusto

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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