Effects of Inter-Set Rest Intervals on Muscle Damage After Flywheel Exercise in Untrained Men (RCT)
25. Juni 2026 aktualisiert von: Federal University of Vicosa
Effects of Different Inter-Set Rest Intervals on Indirect Markers of Muscle Damage and Mechanical Parameters After Flywheel Resistance Training in Untrained Men: A Randomized Parallel-Group Clinical Trial
This randomized parallel-group clinical trial will compare the acute effects of three different inter-set rest intervals during a single lower-limb flywheel resistance exercise session in untrained men.
Participants will be randomly allocated to one of three groups: 1-minute, 2-minute, or 3-minute inter-set rest interval.
The primary outcome will be the change in maximal voluntary isometric contraction of the knee extensors 48 hours after exercise.
Secondary outcomes will include mechanical variables during the exercise session, countermovement jump performance, knee flexor maximal voluntary isometric contraction, muscle soreness, pressure pain threshold, range of motion, ultrasound-derived muscle thickness and echo intensity, perceived exertion, perceived discomfort, perceived recovery status, creatine kinase, and lactate dehydrogenase.
Studienübersicht
Status
Noch keine Rekrutierung
Bedingungen
Detaillierte Beschreibung
Participants will complete seven laboratory visits. The first two visits will be used for baseline assessments and test-retest reliability. The third and fourth visits will be used for technical familiarization with the flywheel exercises. The fifth visit will include the experimental flywheel resistance exercise session and immediate post-exercise assessments. The sixth and seventh visits will include follow-up assessments 48 and 96 hours after the experimental session, respectively. Blood samples for creatine kinase and lactate dehydrogenase will be collected before the experimental session and 72 hours after exercise in a partner laboratory.
The experimental session will include squat, Romanian deadlift, knee extension, and knee flexion exercises performed using flywheel devices. All groups will perform the same exercises, volume, inertia, and execution instructions. The only difference between groups will be the inter-set rest interval: 1 minute, 2 minutes, or 3 minutes.
Studientyp
Interventionell
Einschreibung (Geschätzt)
30
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Minas Gerais
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Viçosa, Minas Gerais, Brasilien, 36570-900
- Federal University of Viçosa
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Kontakt:
- Study Coordinator
- Telefonnummer: (31) 98359-5541
- E-Mail: wanderson.machado@ufv.br
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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
Ja
Beschreibung
Inclusion Criteria:
- Age between 18 and 40 years;
- Apparently healthy and clinically able to perform physical exercise;
- No participation in structured resistance training during the previous 6 months;
- Agreement to comply with all study visits and procedures;
- Signed informed consent form.
Exclusion Criteria:
- History of lower-limb musculoskeletal injury or surgery that may impair performance or safety during the proposed exercise protocol;
- Current pain, injury, or functional limitation in the lower limbs;
- Use of ergogenic aids that may affect physical performance or muscle recovery;
- Use of analgesic or anti-inflammatory medication during the study period;
- Failure to attend the scheduled visits required for the primary outcome assessment.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Grundlegende Wissenschaft
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: 1-Minute Inter-set Rest Interval
Participants allocated to this group will perform a single lower-limb flywheel resistance exercise session using a 1-minute inter-set rest interval.
The session will include squat, Romanian deadlift, knee extension, and knee flexion exercises.
|
Participants will perform a single lower-limb flywheel resistance exercise session using a 1-minute inter-set rest interval.
The session will include squat, Romanian deadlift, knee extension, and knee flexion exercises.
Each exercise will be performed for 4 sets of 2 preparatory repetitions followed by 8 valid repetitions, using the same flywheel inertia, exercise order, and execution instructions across all groups.
Participants will be instructed to perform the concentric phase as fast as possible and to brake the eccentric phase during the final portion of the movement.
The interval between exercises will be standardized at 3 minutes.
|
|
Experimental: 2-Minute Inter-set Rest Interval
Participants allocated to this group will perform a single lower-limb flywheel resistance exercise session using a 1-minute inter-set rest interval.
The session will include squat, Romanian deadlift, knee extension, and knee flexion exercises.
|
Participants will perform a single lower-limb flywheel resistance exercise session using a 2-minute inter-set rest interval.
The session will include squat, Romanian deadlift, knee extension, and knee flexion exercises.
Each exercise will be performed for 4 sets of 2 preparatory repetitions followed by 8 valid repetitions, using the same flywheel inertia, exercise order, and execution instructions across all groups.
Participants will be instructed to perform the concentric phase as fast as possible and to brake the eccentric phase during the final portion of the movement.
The interval between exercises will be standardized at 3 minutes.
|
|
Experimental: 3-Minute Inter-set Rest Interval
Participants allocated to this group will perform a single lower-limb flywheel resistance exercise session using a 1-minute inter-set rest interval.
The session will include squat, Romanian deadlift, knee extension, and knee flexion exercises.
|
Participants will perform a single lower-limb flywheel resistance exercise session using a 3-minute inter-set rest interval.
The session will include squat, Romanian deadlift, knee extension, and knee flexion exercises.
Each exercise will be performed for 4 sets of 2 preparatory repetitions followed by 8 valid repetitions, using the same flywheel inertia, exercise order, and execution instructions across all groups.
Participants will be instructed to perform the concentric phase as fast as possible and to brake the eccentric phase during the final portion of the movement.
The interval between exercises will be standardized at 3 minutes.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in maximal voluntary isometric contraction of the knee extensors
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Maximal voluntary isometric contraction of the knee extensors will be assessed using a load cell with the knee positioned at 90 degrees of flexion.
The primary outcome will be the change in force between baseline and immediately, 48 hours, and 96 hours after the experimental exercise session using a flywheel.
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Change in maximal voluntary isometric contraction of the knee flexors
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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The maximum voluntary isometric contraction of the knee flexors will be assessed using a load cell with the knee positioned at 45 degrees of flexion.
The primary outcome will be the change in force between baseline and immediately, 48 hours, and 96 hours after the experimental exercise session using a flywheel.
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change in vastus lateralis and biceps femoris long head muscle thickness
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Change in vastus lateralis and biceps femoris long head echo intensity
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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|
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Change in countermovement jump performance
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
|
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Change in active and passive knee flexion and extension range of motion
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Change in lower-limb muscle soreness score assessed by the Visual Analogue Scale
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Lower-limb muscle soreness will be assessed using a 100-mm Visual Analogue Scale.
The scale ranges from 0 to 100, where 0 indicates no pain and 100 indicates the worst possible pain.
Higher scores indicate greater muscle soreness.
The outcome will be reported as the change in muscle soreness score from baseline to the post-exercise time points.
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Change in pressure pain threshold of the thigh muscles
Zeitfenster: Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Baseline, 10 minutes after the experimental exercise session, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Change in serum creatine kinase and lactate dehydrogenase concentrations
Zeitfenster: Pre-exercise and 72 hours after the experimental exercise session
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Pre-exercise and 72 hours after the experimental exercise session
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Peak concentric and eccentric power output during flywheel exercise
Zeitfenster: During all 16 sets performed in the experimental exercise session
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Peak concentric and eccentric power output will be recorded during each valid repetition of the flywheel exercise session using a load cell connected to the flywheel device.
Data will be collected for all sets and exercises, excluding the initial preparatory repetitions.
The outcome will be reported as peak concentric power, peak eccentric power, and eccentric/concentric power ratio across the experimental exercise session.
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During all 16 sets performed in the experimental exercise session
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Rating of perceived exertion assessed by the OMNI-Resistance Exercise Scale
Zeitfenster: After each of the 16 sets performed during the experimental exercise session and 10 minutes after the experimental exercise session
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Rating of perceived exertion will be assessed using the OMNI-Resistance Exercise Scale.
The scale ranges from 0 to 10, where 0 indicates extremely easy and 10 indicates extremely hard.
Higher scores indicate greater perceived exertion.
The outcome will be reported after each set of the experimental flywheel exercise session and 10 minutes after the end of the session.
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After each of the 16 sets performed during the experimental exercise session and 10 minutes after the experimental exercise session
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Perceived discomfort assessed by the Discomfort Scale
Zeitfenster: After each of the 16 sets performed during the experimental exercise session and 10 minutes after the experimental exercise session
|
Perceived discomfort will be assessed using a 0-to-100 Discomfort Scale.
The scale ranges from 0 to 100, where 0 indicates no discomfort and 100 indicates maximal discomfort.
Higher scores indicate greater perceived discomfort.
The outcome will be reported after each set of the experimental flywheel exercise session and 10 minutes after the end of the session.
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After each of the 16 sets performed during the experimental exercise session and 10 minutes after the experimental exercise session
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Perceived recovery status assessed by the Perceived Recovery Status Scale
Zeitfenster: Baseline, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
|
Perceived recovery status will be assessed using the Perceived Recovery Status Scale.
The scale ranges from 0 to 10, where 0 indicates very poor recovery and 10 indicates full recovery.
Higher scores indicate better perceived recovery.
The outcome will be reported as the perceived recovery status score at baseline and at the post-exercise follow-up time points.
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Baseline, 48 hours after the experimental exercise session, and 96 hours after the experimental exercise session
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Mitarbeiter und Ermittler
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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)
1. Juni 2026
Primärer Abschluss (Geschätzt)
1. Juli 2026
Studienabschluss (Geschätzt)
1. Juli 2026
Studienanmeldedaten
Zuerst eingereicht
29. Mai 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
25. Juni 2026
Zuerst gepostet (Tatsächlich)
1. Juli 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
1. Juli 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
25. Juni 2026
Zuletzt verifiziert
1. Mai 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- 7.151.525 (Andere Kennung: Ethics Committee Approval Number)
- 81740024.5.0000.5153 (Andere Kennung: CAAE)
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