ClinicalTrials.gg
CompletedNCT07212283LGB-TNBUpdated Oct 1, 2026

Wise Intervention for Reducing Aggressive Behaviors and Promoting Prosocial Behaviors Toward LGB-TNB Individuals

An interventional study of Wise Intervention LGB-TNB and Values alignment wise intervention in Aggression and Adolescence, sponsored by University of Deusto. Completed at 1 site in Spain. Open to participants aged 14 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-01.

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

Updated Oct 1, 2026Now CompletedEnrollment updatedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
1,000
Allocation
Randomized
Ages
14 Years to 18 Years
Sex
All
01

Study summary

This study evaluates the effectiveness of a wise Intervention to reduce aggressive behaviors and promote prosocial behaviors toward LGB-TNB individuals among Spanish adolescents. Half of the participants will receive the experimental intervention, while the other half will receive a control intervention.

Read the detailed description

Discrimination based on sexual orientation and gender identity is a social problem of great relevance. Sexual orientation is understood as the mechanism that directs affective-sexual attraction and interest, manifesting with varying intensity. Regarding gender identity, it has historically been interpreted under a binary paradigm based on external sexual organs, rendering trans and non-binary identities invisible. However, it is currently understood as the internal feeling about one's own gender, so that trans and/or non-binary people represent those whose gender identity differs from the one assigned at birth.

Despite the growing visibility, public awareness, and recognition of the rights of lesbian, gay, bisexual, trans, and non-binary people (LGB-TNB), discrimination based on sexual orientation and gender identity continues to be a social problem of great relevance with serious consequences for those who suffer it. This reality underlines the need to implement effective interventions aimed at addressing these aggressive behaviors and the mechanisms that sustain them, not only among those who perpetrate acts of violence, but also among people who witness these aggressive behaviors.

In addition, intervening during adolescence is especially relevant, as this stage represents a critical moment in the moral, social, and emotional development of individuals. Moreover, during adolescence, discriminatory behaviors and peer aggression increase, and previous studies show that LGB-TNB people face a higher risk of violence in educational settings. Nevertheless, although adolescence becomes a critical period for the development of risk behaviors, it also involves important transitions and learning opportunities. Furthermore, adolescence is a turning point during which well-designed interventions have a high potential to redirect a person's developmental trajectory in a lasting way. Therefore, it can be an especially favorable moment for implementing interventions.

In this way, numerous interventions have been carried out in educational settings to prevent aggressive behaviors among peers. Although most of these initiatives have mainly focused on more general problems, such as bullying and cyberbullying, in recent years preventive interventions specifically aimed at reducing aggressive behaviors based on sexual orientation and gender identity in both face-to-face and digital contexts have increased. However, most current interventions focus on educating people about issues related to LGB-TNB topics, reaching mixed and contradictory results regarding their effectiveness, and also highlighting that there is little empirical evidence about the robustness of the effects of LGB-TNB interventions and their underlying mechanisms. Therefore, these interventions present areas for improvement that constitute important challenges for scientific psychology.

Recently, interest has grown in social psychology regarding a new approach to interventions, which have been called wise interventions. Many of these interventions have impactful results because they are usually very brief in time and produce lasting changes in people's behavior. Moreover, this type of intervention is of great interest in adolescence, as they allow themselves to be designed in such a way that they are perceived as respectful of students' autonomy and status, so that they feel they are making their own decisions.

Therefore, the aim of this project is to adapt to the LGB-TNB context a wise intervention to reduce online and offline aggression among adolescents, especially based on sexual orientation and gender identity, and to increase the intention to support and prosocial behaviors when participants witness these aggressions, especially those directed at LGB-TNB people.

02

Conditions studied

  • Aggression
  • Adolescence

Browse trials for

Keywords

  • Adolescence
  • LGBTQ
  • Aggression
  • Prosocial Behavior
  • Wise Intervention
03

In context

Aggression

248 studies on the registry are indexed under Aggression; 41 are open to participants now.

This study's enrollment of 1,000 is above the median of 80 across 221 interventional studies indexed under Aggression.

Browse Aggression 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
14 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • by the adolescents and their families.
  • To be fluent in Spanish and/or Euskera.

Exclusion criteria

Exclusion Criteria:

  • Lack of permission by families and the adolescent.
  • Lack of understanding of the instructions.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
1,000 participants (actual)

Study arms

  • Active comparator
    Values alignment wise intervention

    Behavioral: Values alignment wise intervention

  • Experimental
    Wise Intervention LGB-TNB

    Behavioral: Wise Intervention LGB-TNB

Interventions

  • BehavioralWise Intervention LGB-TNB

    The intervention will be designed to reduce aggressive behaviors based on sexual orientation and gender identity and to promote prosocial behaviors toward these individuals. This intervention will include three components: (1) reading scientific studies about people's ability to change. In addition, they will read other studies about how thoughts and emotions influence behavior through brain pathways, and that these pathways can be modified under certain circumstances; (2) reading testimonials that support the idea that people can change. These testimonials include accounts of people who were victims or perpetrators based on sexual orientation and gender identity, including important components of empathy and prosocial behaviors toward the victims. To give credibility to the intervention, they will be informed that these stories were written by other young people who previously participated; and (3) self-persuasion exercises that involve an active commitment to change.

  • BehavioralValues alignment wise intervention

    This intervention will be based on the same strategies as the experimental intervention, but it will not address aspects related to prosocial behaviors or aggression toward LGB-TNB individuals; instead, it will be applied to improve adolescents' eating habits.

06

What researchers measure

Primary outcomes

  1. Change from baseline in aggression scores toward LGB-TNB individuals, assessed using an adaptation of the Spanish version (Orue et al., 2018) of the Homophobic Bullying Scale (Prati, 2012).

    It consists of seven items that ask frequency with wich participants have engaged in specific aggressive behavior toward LGB-TNB individuals. Five response categories are provided using a Likert-type response scale, ranging from 1 (never) to 5 (daily).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  2. Change from baseline in online aggression scores toward LGB-TNB individuals, assessed using the Technology-Facilitated Gender- and Sexuality-Based violence (TFGSV; Martínez-Bacaicoa et al., 2023).

    It consists of eight items that ask frequency with wich participants have engaged in online aggressive behavior toward LGB-TNB individuals. Five response categories are provided using a Likert-type response scale, ranging from 1 (never) to 5 (daily).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  3. Change from baseline in prosocial behavior scores toward LGB-TNB individuals through an ad hoc measure.

    It consists of one item in which participants were asked to select all the behaviors they engaged in after witnessing an aggression.

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  4. Change from baseline in bystander intention scores when witnessing aggressive behavior toward LGB-TNB individuals.

    This measure evaluate bystander intentions in response to LGB-TNB aggressions, through different scenarios. After reading the scenarios, participants answered five items that evaluated possible courses of action to take in response to the aggression.

    Time frame: Assessments were conducted at baseline, immediately after the intervention, and at 3, 6, and 9 months.

Secondary outcomes

  1. Change from baseline in moral disengagement scores, assessed using the mechanisms of moral disengagement described by Bandura (2016) and based on studies with similar characteristics (Martínez-Bacaicoa et al., 2024).

    It consists of eight items representing the eight mechanisms that allow participants to morally disengage. Five response categories are provided using a Likert-type response scale, ranging from 1 (strongly disagree) to 5 (strongly agree).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  2. Change from baseline in justice sensitivity scores, assessed using the Justice Sensitivity Inventory (Schmitt et al., 2010).

    It consists of 10 items that assess sensitivity to unjust situations. Five response categories are provided using a Likert-type response scale, ranging from 1 (strongly disagree) to 5 (strongly agree).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  3. Change from baseline in behaviors supporting LGB-TNB individuals, assessed using the LGBT-Affirming Behavior questionnaire (Poteat, 2015).

    It consists of five items that assess supportive behaviors toward LGB-TNB individuals. Five response categories are provided using a Likert-type response scale, ranging from 1 (0 times) to 5 (7 or more times).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  4. Change from baseline in microaggression scores toward LGB-TNB individuals, assessed using the Sexual Orientation Microaggression Scale (SOMS-P; Botor & Tuliao, 2025) and the Gender Identity Microaggression Scale (GIMS-P; Botor & Tuliao, 2025).

    A total of 25 items are used to assess microaggressions toward LGB-TNB individuals. Specifically, 20 items assess microaggressions toward LGB individuals and 5 items assess microaggressions toward TNB individuals. Five response categories are provided using a Likert-type response scale, ranging from 1 (never) to 5 (almost every week).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  5. Change from baseline in offline perpetration scores, assessed using the Spanish adaptation (Ortega-Ruiz et al., 2016) of the European Bullying Intervention Project Questionnaire (Brighi et al., 2012).

    It consists of six items that ask about the frequency with which participants have engaged in aggressive behaviors in offline contexts. Five response categories are provided using a Likert-type response scale, ranging from 1 (never) to 5 (almost every week).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  6. Change from baseline in online perpetration scores, assessed using an adaptation of the Cyberbullying Questionnaire items (Calvete et al., 2010; Gámez-Guadix et al., 2014).

    It consists of five items that ask about the frequency with which participants have engaged in aggressive behaviors in online contexts. Five response categories are provided using a Likert-type response scale, ranging from 1 (never) to 5 (almost every week).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  7. Change from baseline in healthy and unhealthy food intake scores, assessed using an adaptation of the KIDMED 2.0 questionnaire, validated in a sample of Spanish children and adolescents (López-Gajardo et al., 2022).

    It consists of 16 items that ask about the frequency of healthy and unhealthy food intake. Five response categories are provided using a Likert-type response scale, ranging from 1 (never) to 5 (daily).

    Time frame: Assessments were conducted at baseline and at 3, 6, and 9 months.

  8. Change from baseline in alignment of healthy eating habits scores, as assessed by the questionnaire developed by Bryan et al. (2019).

    It consists of seven items that assess the alignment between participants' healthy eating habits and their personal values. Five response categories are provided using a Likert-type response scale, ranging from 1 (strongly disagree) to 5 (strongly agree).

    Time frame: Assessments were conducted at baseline, immediately after the intervention, and at 3, 6, and 9 months.

07

Study locations

1 site
  • Nerea
    Bilbao, BIZKAIA 48007, Spain
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

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, Statistical analysis plan, Informed consent form

Time frame: The study protocol and informed consent protocol will be published at clinicaltrials.org. Data will be available at OSF when the results are published.

Access criteria: Public

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Oct 1, 2026
Show all 1 update
  1. Oct 1, 2026
    Recruiting→Completed
    + 3 other changes: date precision, contact details and site details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07212283
Lead sponsor
University of Deusto
Responsible party
Nerea Cortazar Enciondo (Principal investigator, University of Deusto) — Principal investigator
First posted
Oct 8, 2025
Start date
Sep 18, 2025
Primary completion
Jun 14, 2026
Completion
Jun 14, 2026
Last update
Oct 1, 2026

Oversight

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

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion