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

11 september 2026 bijgewerkt door: 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.

Studie Overzicht

Toestand

Voltooid

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

30

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

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

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Fundamentele wetenschap
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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

Andere namen:
  • 8-Week CrossFit Training Program

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Mean Change in Total Leukocyte Count From Baseline to Completion of the Eight-Week CrossFit Program
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

5 mei 2026

Primaire voltooiing (Werkelijk)

30 juni 2026

Studie voltooiing (Werkelijk)

30 juni 2026

Studieregistratiedata

Eerst ingediend

28 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

11 september 2026

Eerst geplaatst (Werkelijk)

17 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

17 september 2026

Laatste update ingediend die voldeed aan QC-criteria

11 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • KBU-FTB12-2026-002

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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