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The Effects of Caffeine and Vitamin C on Maximum Strength and Strength Endurance in Adolescents With Mild Mental Fatigue

21. Juli 2026 aktualisiert von: Yunliang Zhang

Objective To investigate the independent and combined effects of caffeine and vitamin C on maximal strength and strength endurance in female adolescents with mild mental fatigue.

Methods A randomised, double-blind, crossover experimental design was adopted. Forty female college students presenting mild mental fatigue were recruited as participants. Each participant completed five laboratory sessions in total. The first session determined their one-repetition maximum (1RM) for bench press and back squat. The remaining four experimental sessions involved four supplement interventions administered in random order: placebo control, vitamin C (VC) alone, caffeine (CAF) alone, and combined caffeine plus vitamin C (CAF+VC). A one-week washout interval was arranged between every two supplementation trials.

In each test session, participants completed a 45-min Stroop task to induce mental fatigue prior to exercise assessments. Measurements included the Visual Analogue Scale for Mental Fatigue (VAS-MF), 1RM bench press and squat performance, as well as the maximal number of repetitions at 65% 1RM for both movements. Immediately after the strength endurance test, perceived exertion and muscle pain were rated. Blood glucose and blood lactate concentrations were sampled before and after all exercise protocols.

Supplementation was administered 1 hour prior to testing: a standard caffeine dosage of 3.0 mg per kg body mass and a single 500 mg dose of vitamin C were provided for the corresponding intervention groups.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

40

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • (1) Healthy women aged 18 to 19; (2) No resistance training for at least three months prior to the experiment; (3) All participants had no contraindications to caffeine use and no other medical conditions; (4) Participants were prohibited from using tobacco or e-cigarettes, or from taking any medications, drugs, stimulants, or sports supplements known to interfere with gastric acid production or neuromuscular function during the trial

Exclusion Criteria:

(1) Individuals who have regularly engaged in resistance training over the past 3 months; (2) Individuals with contraindications to caffeine use or other medical conditions; (3) Tobacco or e-cigarette users, or individuals taking any medications, drugs, stimulants, or sports supplements known to interfere with gastric acid production or neuromuscular function during the trial.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Sequenzielle Zuweisung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Kontrolle
A randomized, double-blind, crossover design was employed. Professional coaches assessed the subjects' bench press and back squat performances to examine the effects of caffeine combined with vitamin C on maximum strength (1RM) and strength endurance (repetitions to failure at 65% of 1RM) during bench press and back squat training. 65% of 1RM is a widely recognized load for strength endurance testing [28]. The formal experiment consisted of five test sessions: one for familiarization with the entire experimental procedure and a preliminary 1RM test to reconfirm the 1RM measured three weeks prior to the study. The remaining four sessions were conducted sequentially for the control group, vitamin C (VC), caffeine (CAF), and caffeine plus vitamin C (CAF+VC) groups. Each test was spaced 7 days apart to eliminate carryover effects [30]. All tests were scheduled between 12:00 PM and 4:00 PM to control for the effects of circadian rhythms [30].
Experimental: caf
A randomized, double-blind, crossover design was employed. Professional coaches assessed the subjects' bench press and back squat performances to examine the effects of caffeine combined with vitamin C on maximum strength (1RM) and strength endurance (repetitions to failure at 65% of 1RM) during bench press and back squat training. 65% of 1RM is a widely recognized load for strength endurance testing [28]. The formal experiment consisted of five test sessions: one for familiarization with the entire experimental procedure and a preliminary 1RM test to reconfirm the 1RM measured three weeks prior to the study. The remaining four sessions were conducted sequentially for the control group, vitamin C (VC), caffeine (CAF), and caffeine plus vitamin C (CAF+VC) groups. Each test was spaced 7 days apart to eliminate carryover effects [30]. All tests were scheduled between 12:00 PM and 4:00 PM to control for the effects of circadian rhythms [30].
Experimental: VC
A randomized, double-blind, crossover design was employed. Professional coaches assessed the subjects' bench press and back squat performances to examine the effects of caffeine combined with vitamin C on maximum strength (1RM) and strength endurance (repetitions to failure at 65% of 1RM) during bench press and back squat training. 65% of 1RM is a widely recognized load for strength endurance testing [28]. The formal experiment consisted of five test sessions: one for familiarization with the entire experimental procedure and a preliminary 1RM test to reconfirm the 1RM measured three weeks prior to the study. The remaining four sessions were conducted sequentially for the control group, vitamin C (VC), caffeine (CAF), and caffeine plus vitamin C (CAF+VC) groups. Each test was spaced 7 days apart to eliminate carryover effects [30]. All tests were scheduled between 12:00 PM and 4:00 PM to control for the effects of circadian rhythms [30].
Experimental: caf+VC
A randomized, double-blind, crossover design was employed. Professional coaches assessed the subjects' bench press and back squat performances to examine the effects of caffeine combined with vitamin C on maximum strength (1RM) and strength endurance (repetitions to failure at 65% of 1RM) during bench press and back squat training. 65% of 1RM is a widely recognized load for strength endurance testing [28]. The formal experiment consisted of five test sessions: one for familiarization with the entire experimental procedure and a preliminary 1RM test to reconfirm the 1RM measured three weeks prior to the study. The remaining four sessions were conducted sequentially for the control group, vitamin C (VC), caffeine (CAF), and caffeine plus vitamin C (CAF+VC) groups. Each test was spaced 7 days apart to eliminate carryover effects [30]. All tests were scheduled between 12:00 PM and 4:00 PM to control for the effects of circadian rhythms [30].

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
1RM Squats and Bench Presses;Number of repetitions for 65% 1RM squats and bench presses
Zeitfenster: 5 week
5 week

Mitarbeiter und Ermittler

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Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

25. Juli 2026

Primärer Abschluss (Geschätzt)

20. September 2026

Studienabschluss (Geschätzt)

22. September 2026

Studienanmeldedaten

Zuerst eingereicht

17. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

21. Juli 2026

Zuerst gepostet (Tatsächlich)

24. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

24. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

21. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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JA

Beschreibung des IPD-Plans

http://www.medresman.org.cn/login.aspx

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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