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Strong Minds: A Digital Intervention Targeting Body Image and Psychological Well-being Among Adolescent Male Fitness Club Members (Strong Minds)

2026年8月25日 更新者:Christina Gjestvang、Norwegian School of Sport Sciences

Strong Minds: A Digital Intervention Targeting Body Image and Psychological Well-Being Among Adolescent Male Fitness Club Members

The purpose of this study is to evaluate whether a digital intervention can improve body image and psychological well-being among adolescent boys who attend fitness clubs. Fitness club environments and social media often promote appearance ideals related to muscularity and leanness, which may contribute to body appearance pressure, body dissatisfaction, and psychological distress among boys.

In this cluster-randomized controlled trial, approximately 260 boys aged 15 to 18 years will be recruited from fitness clubs in Oslo, Norway. Participants from fitness clubs assigned to the intervention group will receive access to a 12-week website-based program consisting of four interactive modules focusing on body image, psychological well-being, critical social media literacy, and attitudes toward food and sports supplements. Participants in the control group will continue their usual activities.

The study will examine whether the intervention reduces internalization of appearance ideals and body appearance pressure and improves body appreciation, health-related quality of life, psychological well-being, social media-related behaviors, and attitudes toward food and sports supplements. Outcomes will be assessed at baseline, immediately after the intervention, and at a 6-month follow-up.

調査の概要

詳細な説明

The prevalence of body image concerns among adolescent boys has increased in recent years, accompanied by growing internalization of appearance ideals emphasizing muscularity, leanness, and physical performance. Fitness clubs represent an important social and exercise arena for adolescent boys and may contribute both positively and negatively to psychological well-being. While regular physical activity is associated with health benefits, fitness club environments often expose young males to appearance-focused norms, body comparisons, and social influences reinforced through social media and commercial fitness culture. These factors may increase body appearance pressure, body dissatisfaction, unhealthy attitudes toward food and supplements, and vulnerability to psychological distress. Despite the increasing participation of adolescent boys in fitness clubs, few evidence-based interventions have been developed for this population.

The Strong Minds study aims to evaluate the effectiveness of a digital intervention designed to promote positive body image and psychological well-being among adolescent male fitness club members. The intervention targets body image-related constructs, social media literacy, psychological well-being, and attitudes related to food and sports supplements. The study further seeks to examine mechanisms through which the intervention may influence outcomes, including body appreciation and social media-related processes.

The study will be conducted as a cluster-randomized controlled trial involving fitness clubs in Oslo, Norway. Fitness clubs will serve as the unit of randomization and will be allocated to either an intervention condition or a usual-routine control condition. Approximately 260 participants will be recruited. Data collection will occur at baseline, immediately following the intervention period, and six months after completion of the intervention.

Participants assigned to the intervention group will receive access to a website-based program delivered over 12 weeks. The intervention consists of four modules released at three-week intervals. To maximize engagement and feasibility, the intervention has been designed as a brief and interactive digital experience requiring approximately 75 minutes of total participation. Participants in the control group will continue their usual activities and will receive access to the intervention after study completion.

The intervention content has been developed using evidence-based approaches from body image prevention research, social media literacy interventions, positive psychology, embodiment theory, and sociocultural models of body image development. The website uses an interactive narrative format centered on realistic situations encountered by adolescent boys in fitness club settings. Through short episodes, quizzes, reflection exercises, and individualized feedback, participants are encouraged to critically evaluate appearance ideals, social media messages, body-related pressures, and health information encountered in everyday life. The intervention addresses four core themes: body image, psychological well-being, critical social media literacy, and attitudes toward food and sports supplements.

To enhance relevance, usability, and participant engagement, the intervention will be co-created with a Collaborative Competence Group consisting of young males with lived experience of body image concerns and/or disordered eating related to gym participation. User involvement will contribute to the development of content, design, language, functionality, and overall user experience.

Data will be collected through online questionnaires assessing body image-related constructs, body appreciation, health-related quality of life, psychological distress, social media use and appearance comparison, food-related attitudes, attitudes toward sports supplements, exercise habits, and demographic characteristics. Intervention adherence will be monitored through website analytics, including module completion and login frequency.

The study is funded by the Dam Foundation through ROS (Counselling and Support for Eating Disorders). Ethical approval procedures have been completed in accordance with Norwegian regulations, and all participants will provide informed consent before participation. The findings from the Strong Minds study will contribute to knowledge regarding scalable and accessible strategies for promoting positive body image and psychological well-being among adolescent boys in fitness club environments.

研究の種類

介入

入学 (推定)

260

段階

  • 適用できない

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  • Cisgender boy
  • Aged 15 to 18 years
  • Current member of a fitness club
  • Attends the fitness club at least once per week
  • Able to read and understand Norwegian
  • Provides informed consent (parental/guardian consent required for participants younger than 16 years)

Exclusion Criteria:

  • Does not meet one or more of the inclusion criteria
  • Not able to provide informed consent
  • Previously enrolled in the study

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Digital intervention
Participants assigned to the intervention arm will receive access to a website, a 12-week digital intervention designed to promote positive body image and psychological well-being among adolescent male fitness club members. The intervention consists of four interactive modules released every three weeks and addresses body image, psychological well-being, critical social media literacy, and attitudes toward food and sports supplements. Modules include brief narrative-based content, quizzes, personalized feedback, and reflection exercises. Total engagement time is approximately 75 minutes across the 12-week intervention period.
Participants assigned to the intervention arm will receive access to the Strong Minds website, a 12-week digital intervention designed to promote positive body image and psychological well-being among adolescent male fitness club members. The intervention consists of four interactive modules released every three weeks and addresses body image, psychological well-being, critical social media literacy, and attitudes toward food and sports supplements. Modules include brief narrative-based content, quizzes, personalized feedback, and reflection exercises. Total engagement time is approximately 75 minutes across the 12-week intervention period.
介入なし:Control group
Participants assigned to the control condition will continue their regular exercise and daily activities without receiving the Strong Minds intervention during the 12-week trial period. Outcome assessments will be conducted at the same time points as in the intervention group (baseline, post-intervention, and 6-month follow-up). Access to the digital intervention will be provided after completion of the randomized controlled trial.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Internalization
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Internalization of appearance ideals (Sociocultural Attitudes Towards Appearance Questionnaire-4 [SATAQ-4]). This outcome assesses the extent to which participants adopt societal appearance ideals related to muscularity, leanness, and low body fat as personal standards for evaluating their own appearance. Internalization is measured using the relevant SATAQ-4 subscales. Items are rated on a 5-point Likert scale ranging from 1 (definitely disagree) to 5 (definitely agree), with higher scores indicating greater internalization of societal appearance ideals. The outcome will be assessed at baseline, post-intervention (12 weeks), and 6-month follow-up.
Baseline, post-intervention (12 weeks), and 6-month follow-up.
Body appearance pressure
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Body appearance pressure measured using the Sociocultural Attitudes Towards Appearance Questionnaire-4 Revised (SATAQ-4R). Scores range from 1 to 5, with higher scores indicating greater perceived appearance-related pressure from media and sociocultural influences.
Baseline, post-intervention (12 weeks), and 6-month follow-up.

二次結果の測定

結果測定
メジャーの説明
時間枠
Body appreciation
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
The extent to which participants respect, accept, and value their bodies and maintain a positive body image despite societal appearance pressures.
Baseline, post-intervention (12 weeks), and 6-month follow-up.
Social Media use
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Self-reported social media use, including platform(s) used, frequency of use per day, time spent on social media (hours/day), exposure to appearance-related content, appearance comparison, selfie posting, and motivations for use.
Baseline, post-intervention (12 weeks), and 6-month follow-up.
General health-related quality of life.
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Self-reported health-related quality of life measured using the KIDSCREEN-10 questionnaire. Higher scores indicate better quality of life and well-being.
Baseline, post-intervention (12 weeks), and 6-month follow-up.
Psychological distress
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Psychological distress assessed using the Hopkins Symptom Checklist-10 (HSCL-10). The HSCL-10 is a self-report measure of symptoms of anxiety and depression. The total score is calculated as the mean of the 10 items, with response options ranging from 1 (not at all) to 4 (extremely). Scores range from 1 to 4, with higher scores indicating greater psychological distress and a worse outcome.
Baseline, post-intervention (12 weeks), and 6-month follow-up.
Food-related attitudes.
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Food-related attitudes and behaviors assessed using the Eating Attitudes Test-26 (EAT-26). The EAT-26 is a self-report measure of attitudes, beliefs, and behaviors associated with eating-related concerns and disordered eating. The total score ranges from 0 to 78, with higher scores indicating more problematic eating attitudes and behaviors and a worse outcome. Assessments will be conducted at baseline, post-intervention (12 weeks), and 6-month follow-up.
Baseline, post-intervention (12 weeks), and 6-month follow-up.
Attitudes towards sports supplements
時間枠:Baseline, post-intervention (12 weeks), and 6-month follow-up.
Questions regarding anabolic steroids, testosterone preparations, growth hormone, ephedrine, and Selective Androgen Receptor Modulators (SARMS)) [GU33.1]based on Ungdata, an annual Norwegian data collection scheme.
Baseline, post-intervention (12 weeks), and 6-month follow-up.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2028年1月1日

一次修了 (推定)

2028年9月1日

研究の完了 (推定)

2028年9月1日

試験登録日

最初に提出

2026年8月18日

QC基準を満たした最初の提出物

2026年8月25日

最初の投稿 (実際)

2026年8月27日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月27日

QC基準を満たした最後の更新が送信されました

2026年8月25日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • Strong Minds
  • #SDAM_FOR999270 (その他の助成金/資金番号:The Dam Foundation)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

Individual participant data that have been de-identified, including demographic characteristics, outcome measures, and questionnaire data underlying the published results, will be made available to qualified researchers upon reasonable request following publication of the main study findings. Data sharing will be conducted in accordance with applicable ethical approvals, data protection regulations, and FAIR data principles.

IPD 共有時間枠

Beginning 6 months after publication of the primary study results with no predefined end date.

IPD 共有アクセス基準

Access to de-identified individual participant data will be provided to qualified researchers upon reasonable request. Researchers must submit a methodologically sound research proposal and may be required to sign a data access agreement. Requests will be reviewed by the study investigators to ensure compliance with ethical approvals, applicable data protection regulations, and institutional policies. Data will be shared only for research purposes consistent with the objectives of the original study.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP

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いいえ

米国FDA規制機器製品の研究

いいえ

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