- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07561281
Low-Load BFR vs. High-Load Training on Biceps Hypertrophy
Bayesian Comparison of Low-Load Blood Flow Restriction and High-Load Resistance Exercise on Biceps Brachii Muscle Hypertrophy in Untrained Men
This study aimed to compare the effects of low-load blood flow restriction resistance exercise (BFR-RE) performed to voluntary failure with traditional high-load resistance exercise (HL-RE) and a control condition on biceps brachii muscle hypertrophy, muscle stiffness, and maximal strength in untrained young men.
Participants completed an 8-week training program, with exercise performed three times per week. Outcomes were assessed using ultrasound imaging, elastography, and one-repetition maximum (1RM) testing. The study evaluates whether low-load BFR training can produce adaptations comparable to high-load resistance training.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
This study was designed to examine the efficacy of low-load blood flow restriction resistance exercise (BFR-RE) performed to voluntary failure compared with traditional high-load resistance exercise (HL-RE) in inducing muscular adaptations in untrained individuals. The experimental framework was structured to isolate the effects of mechanical load and metabolic stress by standardizing the selection of exercises and the training frequency across groups.
A controlled, single-blind, repeated-measures design was used, with participants allocated to BFR-RE, HL-RE, or a non-exercising control condition. The intervention period was set at 8 weeks to ensure sufficient exposure for hypertrophic and neuromuscular adaptations, while minimizing potential confounding effects of long-term training variability.
The BFR-RE protocol was developed to emphasize metabolic stress through low external loading (30% 1RM), partial vascular occlusion (60% limb occlusion pressure), and sets performed to volitional failure. In contrast, the HL-RE condition was structured to prioritize mechanical tension using moderate-to-high loading (70% 1RM) without vascular restriction. This contrast enables a mechanistic comparison of two distinct hypertrophic stimuli.
To reduce acute exercise-induced confounding factors, particularly transient muscle swelling, post-intervention assessments were complemented with a delayed follow-up measurement. This approach was incorporated better to reflect true morphological adaptations rather than short-term physiological responses.
The methodological approach integrates imaging-based and performance-based assessments to capture both structural and functional adaptations. The overall design enables evaluation of whether BFR-RE can provide a time-efficient and lower-load alternative to traditional resistance training while maintaining comparable adaptive outcomes.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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Karabük Province
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Karabük, Karabük Province, Türkei (türkiye), 78050
- Karabük University Hasan Dogan Faculty of Sport Sciences
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
Healthy male participants aged 18-30 years No prior history of structured or specialized resistance training targeting the biceps brachii muscle Normotensive (blood pressure <140/90 mmHg) Right-handed (to reduce variability related to limb dominance) Willing to provide written informed consent and comply with the study protocol
Exclusion Criteria:
History of orthopedic injury or musculoskeletal disorder affecting the upper extremities Diagnosis of hypertension (≥140/90 mmHg) or cardiovascular disease Any neurological condition affecting motor performance Current participation in any structured resistance training program Use of medications or supplements known to influence muscle metabolism or performance
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Experimental: BFR-RE
Participants performed low-load resistance exercise with blood flow restriction using 30% of one-repetition maximum (1RM) and 60% limb occlusion pressure.
Exercises were performed to voluntary failure, three times per week for 8 weeks.
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Resistance exercise was performed under partial vascular occlusion using a pneumatic cuff applied to the upper arm.
Limb occlusion pressure was individually determined, and exercise was conducted at a relative intensity corresponding to a percentage of one-repetition maximum.
Occlusion pressure was maintained during sets and released between exercises.
Training load and repetition tempo were standardized and progressively adjusted throughout the intervention period.
Andere Namen:
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Aktiver Komparator: HL-RE
Participants performed traditional high-load resistance exercise at 70% of one-repetition maximum (1RM) without blood flow restriction, three times per week for 8 weeks.
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Participants performed resistance exercise using conventional loading strategies based on a percentage of one-repetition maximum.
Training intensity, volume, and progression were standardized across sessions, with loads adjusted periodically according to performance assessments.
Andere Namen:
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Kein Eingriff: Control
Participants did not engage in any structured resistance training program and continued their normal daily activities throughout the 8-week study period.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Biceps Brachii Muscle Thickness
Zeitfenster: Baseline and 8 weeks (post-intervention), with an additional follow-up measurement at 1 week after the intervention
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Muscle thickness of the biceps brachii was assessed using ultrasound imaging to evaluate hypertrophic adaptations following the intervention.
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Baseline and 8 weeks (post-intervention), with an additional follow-up measurement at 1 week after the intervention
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Andere Studien-ID-Nummern
- Mehmet Akif Ersoy Universitesi
- BFR_HLRE_UntrainedMen (Registrierungskennung: Bayesian Comparison of Low-Load Blood Flow Restriction and High-Load Resistance Exercise on Biceps Brachii Muscle Hyper)
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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