Ta strona została przetłumaczona automatycznie i dokładność tłumaczenia nie jest gwarantowana. Proszę odnieść się do angielska wersja za tekst źródłowy.

Early Time-Restricted Eating in Young Judo Athletes (TRE-JUDO)

25 czerwca 2026 zaktualizowane przez: Maha Gasmi, University of Manouba

Effects of a 5-Month Early Time-Restricted Eating Protocol on Body Composition, Muscle Damage Biomarkers, Competitive Anxiety, and Self-Confidence in Highly Trained Young Judo Athletes: A Randomized Controlled Trial

This study investigates the effects of a 5-month early time-restricted eating (e-TRE) intervention on body composition, muscle damage biomarkers, and psychological variables in highly trained young male judo athletes. One hundred participants were randomly assigned to either an e-TRE group or a control group. The e-TRE group followed a 16:8 fasting protocol (07:00-15:00 eating window) while maintaining their usual training program, whereas the control group maintained habitual dietary patterns. Outcomes included changes in body composition (BMI, body fat, skeletal muscle mass), muscle damage biomarkers (CK, LDH, ASAT, ALAT, uric acid, CRP, total bilirubin), and psychological measures (cognitive anxiety, somatic anxiety, and self-confidence assessed using CSAI-2). Measurements were taken at baseline and after the intervention period. The aim of the study is to determine whether e-TRE can improve physiological recovery and psychological readiness in combat sport athletes without negatively affecting performance-related variables.

Przegląd badań

Szczegółowy opis

This study was designed to evaluate the effects of a 5-month early time-restricted eating (e-TRE) intervention on physiological and psychological outcomes in highly trained young male judo athletes. The study included 100 participants recruited from competitive judo teams in Tunisia. Participants were randomly assigned to either an e-TRE group or a control group in a 1:1 ratio.

The e-TRE group followed a structured 16:8 time-restricted eating protocol, consuming all daily energy intake within an 8-hour window from 07:00 to 15:00, followed by a 16-hour fasting period. During fasting hours, only non-caloric beverages were permitted. The control group maintained their habitual dietary intake and meal timing without any modifications. Both groups continued their regular judo training program, consisting of 5-6 training sessions per week, including technical drills, sparring (randori), and strength and conditioning exercises.

Anthropometric and biochemical measurements were collected at baseline (T0) and after the 5-month intervention (T1). Psychological assessments were conducted before monthly competitions throughout the study period. Blood samples were collected under standardized resting conditions and analyzed using validated enzymatic and immunoassay techniques.

Participants were required to meet strict inclusion criteria, including age 18-26 years, male sex, at least 3 years of judo training experience, and absence of metabolic, psychiatric, or chronic diseases. Exclusion criteria included use of medications or supplements affecting metabolism, prior experience with intermittent fasting, and conditions that could affect training or biomarker outcomes.

The study was approved by the Ethics Committee of the Higher Institute of Sport and Physical Education of Ksar Said, University of Manouba, Tunisia (approval No. 0171823; organization's unique protocol ID: ISSEP-2026-023) and was conducted in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants prior to enrollment

Statistical analyses included repeated-measures ANOVA to assess group × time effects, with significance set at p < 0.05. Effect sizes were calculated using partial eta squared (η²).

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

100

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Manouba
      • Manouba, Manouba, Tunezja, 2009
        • Higher Institute of Sport and Physical Education of Manouba (ISSEP Manouba)

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły

Akceptuje zdrowych ochotników

Tak

Opis

Inclusion Criteria:

  • aged 19-26 years;
  • male judo players; c) with at least 3 years of judo training experience;
  • engaged in judo training 5-6 days per week; e) healthy, with no known chronic illnesses or conditions affecting metabolism, mental health, or physical performance;
  • willing to adhere to a 16:8 e-TRE protocol for the 5-month study period;
  • non-smokers, as smoking may affect anxiety levels and cardiovascular health;
  • not using any performance-enhancing drugs or supplements that could interfere with the study's measurements.

Exclusion Criteria:

  • current musculoskeletal injuries or conditions that could limit participation in training or affect muscle damage biomarkers;
  • diagnosed psychiatric disorders or current treatment for anxiety or mood disorders, as these could interfere with psychological assessments;
  • use of medications affecting metabolism, muscle recovery, or psychological state (e.g., corticosteroids, antidepressants);
  • prior experience with time-restricted eating or intermittent fasting within the past year, as prior adaptation could impact study outcomes;
  • dietary restrictions or practices (e.g., vegan or keto diet) that could affect nutrient intake or metabolic markers;
  • diagnosed sleep disorders or irregular sleep patterns, as sleep quality could impact both muscle recovery and psychological parameters;
  • inability to commit to the structured training program over the study period.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Early Time-Restricted Eating (e-TRE) Group
Participants in this group followed a 16:8 early time-restricted eating protocol for 5 months. Participants maintained their usual training program throughout the intervention period.
The intervention consisted of a 16:8 early time-restricted eating protocol applied for 5 months. Participants consumed all meals between 07:00 and 15:00, followed by a fasting period from 15:00 to 07:00 the next day. Only non-caloric beverages were allowed during fasting hours. Participants continued their regular judo training (5-6 sessions per week) without modifications. Dietary guidance was provided to support adherence to the eating schedule.
Brak interwencji: Control Group
Participants in this group maintained their habitual dietary practices. They continued their regular judo training program throughout the 5-month study period.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Competitive Anxiety and Self-Confidence
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)

Competitive anxiety and self-confidence will be assessed using the Competitive State Anxiety Inventory-2 (CSAI-2). This validated questionnaire measures three dimensions of pre-competition psychological state: cognitive anxiety, somatic anxiety, and self-confidence. Scores will be used to evaluate changes in athletes' psychological readiness, emotional response to competition, and perceived self-efficacy.

The CSAI-2 consists of 27 items, divided into three subscales (9 items each). Each item is rated on a 4-point Likert scale ranging from 1 ("not at all") to 4 ("very much so"). Subscale scores are calculated by summing item responses, resulting in a score range of 9 to 36 for each dimension (cognitive anxiety, somatic anxiety, and self-confidence).

Measurements will be taken at baseline (T0) and post-intervention (T1) to determine the effect of early time-restricted eating on competitive anxiety and self-confidence in young judo athletes.

Baseline and 5 months (pre-intervention and post-intervention)
Creatine kinase (CK)
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)]
Creatine kinase (CK) will be used as a marker of muscle damage. Blood samples will be collected to assess changes in CK levels in response to the early time-restricted eating intervention. CK concentrations will be measured in U/L and compared between baseline (T0) and post-intervention (T1, 5 months) in judo athletes.
Baseline and 5 months (pre-intervention and post-intervention)]
Lactate dehydrogenase (LDH)
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Lactate dehydrogenase (LDH) will be used as a biomarker of muscle damage. LDH will be measured in U/L to assess changes induced by early time-restricted eating between baseline and post-intervention in judo athletes.
Baseline and 5 months (pre-intervention and post-intervention)
Aspartate aminotransferase (AST)
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Aspartate aminotransferase (AST) will be measured as an indirect marker of muscle damage and metabolic stress. AST levels will be assessed in U/L to evaluate changes from baseline to post-intervention following early time-restricted eating in judo athletes.
Baseline and 5 months (pre-intervention and post-intervention)
Alanine aminotransferase (ALT)
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Alanine aminotransferase (ALT) will be assessed as a biomarker related to muscle stress. ALT levels will be measured in U/L to determine changes following early time-restricted eating between baseline and post-intervention in judo athletes.
Baseline and 5 months (pre-intervention and post-intervention)
Uric acid
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Uric acid will be measured as a metabolic and oxidative stress biomarker. Serum uric acid will be assessed in µmol/L to evaluate changes induced by early time-restricted eating in judo athletes.
Baseline and 5 months (pre-intervention and post-intervention)
C-reactive protein (CRP)
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
C-reactive protein (CRP) will be used as a systemic inflammation biomarker. CRP levels will be measured in mg/L to assess inflammatory response changes following early time-restricted eating between baseline and post-intervention in judo athletes.
Baseline and 5 months (pre-intervention and post-intervention)
Total bilirubin
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Total bilirubin will be measured as a marker of oxidative stress and heme metabolism. Serum bilirubin levels will be assessed in µmol/L to evaluate changes induced by early time-restricted eating in judo athletes between baseline and post-intervention.
Baseline and 5 months (pre-intervention and post-intervention)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Body Mass Index (BMI)
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Body Mass Index (BMI) will be calculated as body weight in kilograms divided by height in meters squared (kg/m²). BMI will be used to assess changes in overall body composition status following early time-restricted eating.
Baseline and 5 months (pre-intervention and post-intervention)
Body fat percentage
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Body fat percentage will be assessed as an indicator of relative adiposity. Body fat percentage will be expressed as a percentage (%) and measured to evaluate changes following the early time-restricted eating intervention.
Baseline and 5 months (pre-intervention and post-intervention)
Skeletal muscle mass
Ramy czasowe: Baseline and 5 months (pre-intervention and post-intervention)
Skeletal muscle mass will be assessed as an indicator of lean muscle tissue. Skeletal muscle mass will be measured in kilograms (kg) to evaluate changes induced by early time-restricted eating.
Baseline and 5 months (pre-intervention and post-intervention)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Współpracownicy

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

1 stycznia 2026

Zakończenie podstawowe (Rzeczywisty)

20 stycznia 2026

Ukończenie studiów (Rzeczywisty)

6 czerwca 2026

Daty rejestracji na studia

Pierwszy przesłany

19 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

25 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

26 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

26 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

25 czerwca 2026

Ostatnia weryfikacja

1 czerwca 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Opis planu IPD

There is no plan to share individual participant data. Only aggregate study results will be reported in publications and presentations.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Subskrybuj