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Effects of CrossFit Training on the Immune System (CFIT-IMMUNE)

11 septembre 2026 mis à jour par: Assoc. Prof. Dr. Özgür EKEN, Inonu University

From Acute Response to Chronic Adaptation: Immunological Effects of an Eight-Week CrossFit Training Program in Sedentary Adults

This interventional study aims to investigate the effects of both acute and eight-week CrossFit training on immune system responses in sedentary adults. Participants will undergo an acute CrossFit exercise session, followed by an eight-week supervised CrossFit training program. Blood samples will be collected before and after the acute exercise session and again following the eight-week intervention to evaluate changes in selected immune system biomarkers. The primary objective is to determine whether acute and chronic CrossFit training induces significant alterations in immune function in previously sedentary individuals. The findings are expected to contribute to a better understanding of the immunological adaptations associated with high-intensity functional training and to provide evidence regarding the safety and potential health benefits of CrossFit exercise in sedentary populations.

Aperçu de l'étude

Statut

Complété

Description détaillée

CrossFit is a high-intensity functional training (HIFT) program that combines aerobic exercise, resistance training, weightlifting, gymnastics, and metabolic conditioning within a single exercise session. Owing to its increasing popularity among both athletes and the general population, there is growing interest in understanding the physiological and immunological adaptations associated with CrossFit training. Although regular physical activity is known to enhance immune function and improve overall health, high-intensity exercise may induce transient alterations in immune responses, particularly in previously sedentary individuals.

The immune system plays a critical role in protecting the body against infections and maintaining physiological homeostasis. Acute bouts of strenuous exercise may temporarily modify immune cell function and inflammatory responses, whereas long-term exercise training may promote beneficial adaptations and improve immune regulation. However, the effects of CrossFit training on immune system biomarkers in sedentary adults remain insufficiently investigated.

The purpose of this interventional study is to evaluate the effects of both an acute CrossFit exercise session and an eight-week supervised CrossFit training program on immune system responses in sedentary adults. Participants will complete baseline assessments followed by an acute CrossFit exercise session. Subsequently, they will participate in an eight-week supervised CrossFit training program. Blood samples will be collected at predetermined time points before and after the acute exercise session and following completion of the eight-week intervention to assess changes in immune system biomarkers.

The primary objective is to determine whether acute and chronic CrossFit training produce significant changes in immune function in sedentary individuals. The results of this study are expected to improve understanding of the immunological responses to high-intensity functional training and provide evidence regarding the safety and potential health benefits of CrossFit exercise for previously sedentary adults.

Type d'étude

Interventionnel

Inscription (Réel)

30

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Karabük Province
      • Karabük, Karabük Province, Turquie (Türkiye)
        • Exercise Physiology Laboratory, Faculty of Sport Sciences, Karabuk University

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:- Male participants aged 18 to 23 years

  • Currently enrolled as a student at Yalova University
  • Not regularly participating in exercise or sports training
  • Medically eligible to participate in CrossFit training
  • Willing and able to complete the eight-week CrossFit training program conducted three days per week
  • Willing to provide venous blood samples at the specified assessment times
  • Willing to provide written informed consent

Exclusion Criteria:- Regular participation in exercise or sports training

  • History of a neurological disorder within the previous year
  • History of an auditory, visual, or vestibular disorder within the previous year
  • Serious upper- or lower-extremity injury within the previous six months
  • Presence of a medical condition that could prevent safe participation in the exercise program
  • Inability to complete the training or blood-sampling procedures
  • Withdrawal of voluntary consent

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: CrossFit Training
Participants assigned to the CrossFit Training Group will participate in a structured CrossFit exercise program for 8 weeks. Training sessions will be performed three times per week under the supervision of certified trainers. Each session will include warm-up, functional strength exercises, high-intensity metabolic conditioning exercises, and cool-down periods. Exercise intensity will be monitored throughout the intervention period.

articipants in the experimental group will participate in an eight-week CrossFit training program performed three days per week (Monday, Wednesday, and Friday). Each training session will last approximately 60 minutes and will include a dynamic warm-up, strength training exercises, a Workout of the Day (WOD) section, and a cool-down period.

The strength training component will include functional resistance exercises such as squats, deadlifts, and push presses, performed for 3-5 sets of 5-10 repetitions. Training intensity will progressively increase from approximately 60-70% of one-repetition maximum (1RM) during the first four weeks to 70-80% of 1RM during the final four weeks.

The WOD component will include high-intensity functional exercises such as burpees, kettlebell swings, box jumps, rowing, sit-ups, pull-ups, and short-distance running. WOD sessions will be performed using AMRAP (As Many Rounds As Possible) and For Time formats with durations of approximately 10-20 minutes. P

Autres noms:
  • 8-Week CrossFit Training Program

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Mean Change in Total Leukocyte Count From Baseline to Completion of the Eight-Week CrossFit Program
Délai: Baseline and immediately after completion of the eight-week CrossFit training program
Total leukocyte count will be determined from venous blood samples collected before the first training session and immediately after completion of the eight-week CrossFit training program. For each participant, the change will be calculated as the post-program value minus the baseline value. The group-level outcome will be summarized using the mean change and standard deviation.
Baseline and immediately after completion of the eight-week CrossFit training program
Mean Change in Absolute Monocyte Count From Baseline to Completion of the Eight-Week CrossFit Program
Délai: Baseline and immediately after completion of the eight-week CrossFit training program
Absolute monocyte count will be determined from venous blood samples collected before the first training session and immediately after completion of the eight-week CrossFit training program. For each participant, the change will be calculated as the post-program value minus the baseline value. The group-level outcome will be summarized using the mean change and standard deviation.
Baseline and immediately after completion of the eight-week CrossFit training program
Mean Change in Absolute Lymphocyte Count From Baseline to Completion of the Eight-Week CrossFit Program
Délai: Baseline and immediately after completion of the eight-week CrossFit training program
Absolute lymphocyte count will be determined from venous blood samples collected before the first training session and immediately after completion of the eight-week CrossFit training program. For each participant, the change will be calculated as the post-program value minus the baseline value. The group-level outcome will be summarized using the mean change and standard deviation.
Baseline and immediately after completion of the eight-week CrossFit training program
Mean Change in Absolute Neutrophil Count From Baseline to Completion of the Eight-Week CrossFit Program
Délai: Baseline and immediately after completion of the eight-week CrossFit training program
Absolute neutrophil count will be determined from venous blood samples collected before the first training session and immediately after completion of the eight-week CrossFit training program. For each participant, the change will be calculated as the post-program value minus the baseline value. The group-level outcome will be summarized using the mean change and standard deviation.
Baseline and immediately after completion of the eight-week CrossFit training program

Collaborateurs et enquêteurs

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

5 mai 2026

Achèvement primaire (Réel)

30 juin 2026

Achèvement de l'étude (Réel)

30 juin 2026

Dates d'inscription aux études

Première soumission

28 juillet 2026

Première soumission répondant aux critères de contrôle qualité

11 septembre 2026

Première publication (Réel)

17 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

17 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

11 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • KBU-FTB12-2026-002

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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