Tämä sivu käännettiin automaattisesti, eikä käännösten tarkkuutta voida taata. Katso englanninkielinen versio lähdetekstiä varten.

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

perjantai 11. syyskuuta 2026 päivittänyt: 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.

Tutkimuksen yleiskatsaus

Yksityiskohtainen kuvaus

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.

Opintotyyppi

Interventio

Ilmoittautuminen (Todellinen)

30

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskelupaikat

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

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen

Hyväksyy terveitä vapaaehtoisia

Joo

Kuvaus

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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Perustiede
  • Jako: Ei käytössä
  • Inventiomalli: Yksittäinen ryhmätehtävä
  • Naamiointi: Ei mitään (avoin tarra)

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: 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

Muut nimet:
  • 8-Week CrossFit Training Program

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Mean Change in Total Leukocyte Count From Baseline to Completion of the Eight-Week CrossFit Program
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Sponsori

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Todellinen)

Tiistai 5. toukokuuta 2026

Ensisijainen valmistuminen (Todellinen)

Tiistai 30. kesäkuuta 2026

Opintojen valmistuminen (Todellinen)

Tiistai 30. kesäkuuta 2026

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Tiistai 28. heinäkuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Perjantai 11. syyskuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Torstai 17. syyskuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Torstai 17. syyskuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Perjantai 11. syyskuuta 2026

Viimeksi vahvistettu

Tiistai 1. syyskuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muut tutkimustunnusnumerot

  • KBU-FTB12-2026-002

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

EI

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .

Tilaa