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Building Resilience in Cyberbullying Victims

NCT04509531 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 850

Last updated 2021-09-28

No results posted yet for this 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.

Conditions

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

Interventions

BEHAVIORAL

Wise 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.

BEHAVIORAL

Standard preventive intervention

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

Sponsors & Collaborators

  • Fundación Alicia Koplowitz

    collaborator UNKNOWN

  • University of Deusto

    lead OTHER

Principal Investigators

  • Esther Calvete, PhD · University of Deusto

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
11 Years
Max Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-09-15
Primary Completion
2021-07-31
Completion
2021-07-31

Countries

  • Spain

Study Locations

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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 NCT04509531 on ClinicalTrials.gov