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Calisthenics-Based Intervention in Adolescents: Effects on Strength, Body Composition, Eating Habits, and Self-Concept (CALI-TEENS)

7 maggio 2026 aggiornato da: José Serrano, Universitat de Lleida

School-Based Calisthenics Intervention for Promoting Physical Activity in Adolescents

This study evaluates the effectiveness of a school-based calisthenics intervention in promoting physical activity and improving health-related outcomes in adolescents. Physical inactivity during adolescence is a growing public health concern associated with increased risks of obesity, poor physical fitness, and reduced psychological well-being. Schools provide an optimal environment to implement structured interventions that encourage lifelong healthy habits.

Calisthenics is a form of exercise that uses bodyweight movements to improve strength, flexibility, and coordination. It is cost-effective, accessible, and does not require specialized equipment, making it particularly suitable for school settings. The present study integrates a structured calisthenics program into regular physical education classes.

A total of 100 students aged 13 to 16 years will be randomly assigned to either an experimental group, which will participate in the calisthenics program, or a control group, which will follow the standard physical education curriculum. The intervention will last 12 weeks, with three sessions per week.

Primary and secondary outcomes will be assessed at baseline and after the intervention. These include physical fitness (muscle strength), body composition, dietary habits, and self-concept. Strength will be measured using a handgrip dynamometer, body composition through anthropometric assessment, dietary habits through a validated questionnaire, and self-concept using the Self-Concept Form-5 (AF5).

Findings from this study will provide evidence regarding the feasibility and effectiveness of implementing calisthenics in school settings as a strategy to improve both physical and psychological health in adolescents.

Panoramica dello studio

Descrizione dettagliata

Study Design This is a randomized, parallel-group, controlled trial designed to assess the effects of a school-based calisthenics intervention on physical fitness, body composition, dietary habits, and self-concept in adolescents. Participants will be randomly assigned in a 1:1 ratio to an experimental group or a control group.

Study Setting The study will be conducted at a public secondary school in Turmequé, Boyacá, Colombia, involving ninth-grade students.

Participants A total of 120 adolescents aged between 13 and 16 years will be recruited. Eligibility will be determined based on predefined inclusion and exclusion criteria. Written informed consent from parents or legal guardians and assent from participants will be obtained prior to enrollment.

Randomization and Allocation Participants will be assigned to study groups using a computer-generated randomization sequence. Allocation will be conducted by an independent individual not directly involved in the study procedures to minimize selection bias. Due to the nature of the intervention, participant blinding is not feasible.

Intervention The experimental group will participate in a structured calisthenics program integrated into physical education classes over a 12-week period. The program consists of three weekly sessions of approximately 60 minutes each.

Each session will include the following components:

  • Warm-up phase (mobility and dynamic stretching)
  • Main exercise phase, including six bodyweight exercises targeting upper body, lower body, or full-body strength
  • Cool-down phase with static stretching and relaxation exercises

The intervention follows a progressive overload model:

Exercise duration will increase over time (from 60 to 90 seconds per exercise) Rest intervals between sets will decrease progressively (from 40 to 15 seconds) Effort intensity will be monitored using the Borg Rating of Perceived Exertion scale

Sessions will be conducted in school facilities, including outdoor spaces and sports courts, under the supervision of a qualified instructor to ensure safety and proper execution.

Control Group Participants in the control group will continue with their standard physical education curriculum, which includes activities such as volleyball and handball, according to the institutional academic plan.

Outcome Measures Assessments will be conducted at baseline (week 0) and post-intervention (week 13).

Primary Outcomes

- Muscle strength: measured using a digital handgrip dynamometer

Secondary Outcomes

  • Body composition: assessed through anthropometric measurements and skinfold thickness to estimate body fat percentage and body mass index
  • Dietary habits: evaluated using a validated food frequency questionnaire
  • Self-concept: assessed using the Self-Concept Form-5 (AF5), which measures multiple dimensions including physical self-perception

Sample Size Calculation The sample size was calculated to detect a meaningful difference in strength outcomes between groups, assuming a standard deviation of 15 units, with 90% power and a 5% significance level. A minimum of 60 participants per group is required.

Statistical Analysis Descriptive statistics will be calculated for all variables. Normality will be assessed using the Kolmogorov-Smirnov test. A two-way analysis of variance (ANOVA) will be performed to examine the effects of time, group, and their interaction. Bonferroni post hoc tests will be applied where appropriate. Statistical significance will be set at p < 0.05.

Data Management Participant data will be coded to ensure confidentiality. Only authorized research personnel will have access to the dataset. Data will be stored securely and managed in accordance with data protection regulations.

Ethical Considerations The study will be conducted in accordance with the principles of the Declaration of Helsinki and applicable national and international regulations. The study involves minimal risk, as it consists of supervised physical activity within a school setting. Participants will be informed that their participation is voluntary and that they may withdraw at any time without consequences.

Expected Impact This study aims to provide evidence on the effectiveness of calisthenics as a low-cost, accessible intervention to promote physical activity and improve health outcomes in adolescents. The results may contribute to the development of innovative physical education strategies and inform public health policies targeting youth populations.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

100

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Departamento de Boyacá
      • Turmequé, Departamento de Boyacá, Colombia, 153060
        • Institución Educativa Técnica Industrial de Turmequé-Boyacá

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

Descrizione

Inclusion Criteria:

  • Enrollment in the ninth grade at the Institución Educativa Técnica Industrial de Turmequé, Boyacá.
  • Age between 13 and 16 years.
  • Agreement to random group assignment.

Exclusion Criteria:

  • Presence of medical conditions or disorders that could contraindicate physical exercise, including but not limited to cardiac arrhythmias, heart murmurs, coronary artery disease, or hypertension, as diagnosed by a physician at the start of the calisthenics program.
  • Presence of psychiatric disorders, such as severe anxiety attacks or depression, diagnosed by a qualified healthcare professional at the beginning of the calisthenics program.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Calisthenics
Calisthenics 12 week, 3 times per week, exercise program
12 week exercise program, with a frequency of 3 times per week and a duration of 1 hour per session
Comparatore attivo: Control
School exercise programm
Physical activity following School Education Program

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Hand grip strenght
Lasso di tempo: From enrollment to the end of the intervention at 12 weeks
Handgrip strength is assessed using a handheld dynamometer to evaluate muscular strength. Participants are instructed to squeeze the device with maximal effort, usually with the dominant hand, for a few seconds. The highest value from repeated trials is recorded in kilograms or newtons
From enrollment to the end of the intervention at 12 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Percentage of body fat
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Skinfold anthropometric measurements will be determined to estimate body fat. The thickness of subcutaneous fat at the biceps, triceps, subscapular and suprailiac sites using standarized calipers will be performed. These values will be applied to equations to calculate body density and, from it, body fat percentage.
From enrollment to the end of treatment at 12 weeks
Dietary habits
Lasso di tempo: From enrollment to the end of treatment at 12 weeks
Self-report of habitual food frequency consumption using a standardized and validated questionnaire. Briefly, it consists of a 33-item questionnaire including foods commonly consumed by the selected study group.
From enrollment to the end of treatment at 12 weeks
Self-concept
Lasso di tempo: From enrollment to the end to the treatment at 12 weeks
Reported by each volunteer using the AF5 Self-Concept Questionnaire, a validated instrument that assesses self-concept across five dimensions (academic/work, social, emotional, family, and physical) using a Likert-type scale, where higher scores indicate a more positive self-perception in each domain.
From enrollment to the end to the treatment at 12 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Jose CE Serrano, PhD, Universitat de Lleida

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

15 gennaio 2024

Completamento primario (Effettivo)

15 settembre 2025

Completamento dello studio (Effettivo)

15 dicembre 2025

Date di iscrizione allo studio

Primo inviato

29 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

7 maggio 2026

Primo Inserito (Effettivo)

13 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

13 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • CALI-TEENS
  • Universitat de Lleida (Identificatore di registro: Escola de Doctorat)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano IPD

Individual participant data are not publicly available due to ethical and privacy restrictions. However, de-identified data may be made available from the corresponding author upon reasonable request and with approval from the institutional ethics committee.

Periodo di condivisione IPD

January 2026 util January 2036

Criteri di accesso alla condivisione IPD

Upon request by e-mail

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • RSI

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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