Use of Football in Programs to Reduce Stigma Toward Mental Illness: A Comparison of the Effectiveness of Contact Interaction and Video-Based Approaches

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorKaohsiung Medical University Chung-Ho Memorial Hospital

About this trial

The goal of this clinical trial is to evaluate the effectiveness of football-based interventions in reducing stigma toward mental illness among university students. The main questions it aims to answer are:

* Does participating in a contact-based education program involving football help reduce stigma toward mental illness among university students? * What are the effects of three different intervention methods on reducing stigma toward mental illness?

Researchers will compare the traditional contact-based education program with the other two interventions to evaluate their differences in effectiveness.

Participants will:

* Be randomly assigned to one of the three intervention groups. * Complete online assessments to measure attitudes toward mental illness before and after the intervention. * Participate in qualitative interviews to provide in-depth feedback on their experiences and perceptions.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

University students currently enrolled, aged between 18 and 30 years.

In good physical condition with no contraindications to exercise (i.e., not diagnosed by a physician or advised to avoid physical activity, and with no items selected on the PAR-Q+ [Physical Activity Readiness Questionnaire for Everyone]).

Able to follow the study procedures and provide signed informed consent.

Disqualifiers

Individuals who are unable to safely participate in football activities due to intellectual disability, pregnancy, head injury, cardiovascular disease, or other neuromuscular or musculoskeletal disorders.

Individuals who are unable to effectively participate in the intervention program or complete assessments due to significant emotional disturbances, personality disorders, substance (alcohol) abuse, or severe mental illness.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Contact-Based Education

    Behavioral

    A one-time session lasting approximately 1.5 to 2.5 hours, consisting of psychiatric education, storytelling by individuals with mental illness, and interactive discussion.

  • Video + Contact-Based Education

    Behavioral

    A one-time session lasting approximately 1.5 to 2.5 hours, including football video viewing, psychiatric education, storytelling by individuals with mental illness, and interactive discussion.

  • Football + Contact-Based Education

    Behavioral

    A one-time session lasting approximately 1.5 to 2.5 hours. The session includes football interactive activities, football video viewing, psychiatric education, storytelling by individuals with mental illness, and interactive discussion.

Treatment groups

210 Participants
are divided into 3 treatment groups
Group A: Contact-based educationActive comparator 1 intervention
Group B: Video and contact-based educationExperimental treatment 1 intervention
Group C: Football and contact-based educationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Knowledge

The Mental Health Knowledge Schedule (MAKS), consisting of 12 items, will be used to assess the public's knowledge related to mental health stigma. The questionnaire is divided into two parts: knowledge about mental illness and agreement with statements regarding mental health conditions. Responses are rated on a five-point Likert scale (5 = Strongly agree, 4 = Slightly agree, 3 = Neither agree nor disagree / Don't know, 2 = Slightly disagree, 1 = Strongly disagree). The total score ranges from 12 to 60, with higher scores indicating a greater level of knowledge about mental health. Items 7 to 12 are designed to assess recognition and familiarity with various mental health conditions, helping to contextualize responses to the earlier items.

Time frame
pre-intervention, immediately post-intervention, and at one- and six-month follow-ups.
2

Attitudes

The Questionnaire on Stigmatizing Attitudes Towards Mental Illness will be used in this study. After undergoing cultural adaptation and psychometric validation, the final Chinese version consists of 16 items across four dimensions: Negative Stereotypes (5 items), Social Distance (3 items), Negative Evaluation (5 items), and Self-Stigma (3 items). Responses are measured on a six-point Likert scale (6 = Strongly agree, 5 = Agree, 4 = Slightly agree, 3 = Slightly disagree, 2 = Disagree, 1 = Strongly disagree). The total score ranges from 16 to 96, with higher scores indicating greater levels of negative stigmatizing attitudes toward mental illness.

Time frame
pre-intervention, immediately post-intervention, and at one- and six-month follow-ups.
3

Intent

The Social Distance Scale will be adopted to assess participants' level of social distance toward individuals with mental illness, serving as an indicator of intent to act. The scale consists of 8 items, which evaluate willingness to engage with people with mental illness in various situations, such as living in the same community or building, sharing a residence, dining together, forming friendships, working together, employing, or helping them. Responses are rated on a six-point Likert scale (6 = Strongly agree, 5 = Agree, 4 = Slightly agree, 3 = Slightly disagree, 2 = Disagree, 1 = Strongly disagree). Higher scores indicate a greater willingness to interact with individuals with mental illness. This scale is considered to be particularly sensitive to measuring implicit bias.

Time frame
pre-intervention, immediately post-intervention, and at one- and six-month follow-ups.

Secondary outcomes

Other outcomes

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