- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07619612
Home-Based Circuit Training in Adults With Obesity (HBCT)
Effects of Home-Based Circuit Training on Vascular and Metabolic Health in Adults With Obesity: A Randomized Controlled Trial
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Obesity is a major public health concern associated with endothelial dysfunction, arterial stiffness, metabolic impairment, and reduced physical fitness. Although exercise training is recommended for obesity management, adherence to supervised exercise programs may be limited by time constraints and accessibility. Home-based circuit training may provide a feasible alternative that combines aerobic and resistance exercise within a time-efficient format.
This randomized controlled trial investigates the effects of a 12-week home-based circuit training intervention on vascular function, body composition, metabolic function, resting metabolic rate, substrate oxidation, physical activity, and physical fitness in adults with obesity.
Participants with obesity (BMI ≥ 27.5 kg/m²) will be randomly assigned to either a circuit training group or a control group. The intervention group will perform home-based circuit training using light-to-moderate resistance three times weekly for 12 weeks, while the control group will maintain usual activities.
Primary vascular outcomes include flow-mediated dilation, carotid intima-media thickness, brachial-ankle pulse wave velocity, and post-occlusive reactive hyperemia. Secondary outcomes include body composition, fasting plasma glucose, resting metabolic rate, substrate oxidation, physical activity, muscular strength, flexibility, and cardiorespiratory fitness.
The study aims to determine whether home-based circuit training can improve vascular and metabolic health and serve as a practical strategy for reducing cardiovascular risk in adults with obesity.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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ฺBangkok
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Bangkok, ฺBangkok, Thailand, 10330
- Faculty of Sports Science, Chulalongkorn University
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Adults with obesity according to the Asia-Pacific criteria (body mass index [BMI] ≥ 27.5 kg/m²).
- Able to participate in a home-based exercise program.
- Willing to provide written informed consent.
Exclusion Criteria:
- History of uncontrolled diabetes (HbA1c ≥ 10% or blood glucose ≥ 200 mg/dL).
- Uncontrolled hypertension (≥ 140/90 mmHg).
- Cardiovascular disease.
- Chronic obstructive pulmonary disease.
- Orthopedic conditions limiting exercise participation.
- Participation in regular exercise programs or sports activities within the previous 3 months
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Experimental: Home-Based Circuit Training
Participants in this group will perform a 12-week home-based circuit training program three times per week.
Each session includes warm-up, circuit exercise, and cool-down components designed to improve vascular and metabolic health.
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Participants will perform a 12-week home-based circuit training program three times per week. Each session includes warm-up, circuit-based exercises targeting major muscle groups, and cool-down activities. The intervention is designed to improve vascular and metabolic health in adults with obesity. The training program consisted of two phases: phase 1 (weeks 1-6) and phase 2 (weeks 7-12). During phase 1, participants performed resistance exercises at an intensity of 65-70% of one-repetition maximum (1RM). Each exercise consisted of 12 repetitions, with a 1-minute rest between exercises. The lifting tempo was maintained at 2:2 (concentric: eccentric). Participants completed 8 exercises per circuit for a total of 3 circuits, with a 2-minute rest between circuits. During phase 2, the intensity was increased to 70-75% of 1RM, while maintaining 12 repetitions per exercise. The rest interval between exercises was reduced to 30 seconds, with the same lifting tempo (2:2). Participants complete |
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Kein Eingriff: Control Group
participants in the control group will maintain their usual daily activities without participating in the exercise intervention during the study period.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Vascular Function
Zeitfenster: Baseline and 12 weeks
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Change in flow-mediated dilation from baseline to 12 weeks.
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Baseline and 12 weeks
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Mitarbeiter und Ermittler
Sponsor
Ermittler
- Studienleiter: Daroonwan Suksom, PhD, Faculty of Sports Science, Chulalongkorn University, Bangkok, Thailand
- Hauptermittler: Tunyakarn Worasettawat, PhD, Faculty of Sports Science, Chulalongkorn University, Bangkok, Thailand
- Studienstuhl: Hirofumi Tanaka, PhD, Department of Kinesiology and Health Education, The University of Texas at Austin, USA
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
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- HBCT-OB-2026
- Ratchadapisek Postdoctoral (Andere Zuschuss-/Finanzierungsnummer: Chulalongkorn University)
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
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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