Effect of 8 Weeks of Resistance Training With Blood Flow Restriction on Muscle Strength, Clinical Parameters, Biochemical Biomarkers, and Perceived Exertion in Adults With Obesity
Centro Universitario de Tlajomulco, Universidad de Guadalajara
Phase
Not applicable
Started
2026-02-01
Last updated
2026-03-03
Condition(s) studied
Obesity & Overweight
Investigational drug(s) / intervention(s)
InterventionIntervention
Intervention: The BFR group will perform machine-based quadriceps extension exercises and dumbbell biceps curls involving both lower limbs and both upper limbs. Each exercise will consist of 4 sets of 12 repetitions. Quadriceps extensions will be performed at an intensity of 40% of one-repetition maximum (1RM), and biceps curls at 20% of 1RM. The execution cadence will be standardized to 1 second for the concentric phase and 2 seconds for the eccentric phase. Inter-set rest intervals will be 1 minute. For vascular occlusion, a Carbafix cuff (8 cm width × 68 cm length for the upper limb; 10.5 cm width × 106.0 cm length for the lower limb) will be applied directly to the skin at the most proximal portion of the arm or thigh. The cuff will be inflated to 20 mmHg above resting brachial systolic blood pressure. To ensure partial vascular occlusion, pulse and oxygen saturation will be assessed using a pulse oximeter at the end of each set. Cuff pressure will be released during the inter-set rest periods.
Intervention: The control group will perform quadriceps extensions and biceps curls, completing 4 sets of 10 repetitions at an intensity of 70% of one-repetition maximum (1RM). The execution tempo will be standardized to 1 second for the concentric phase and 2 seconds for the eccentric phase, with 2-minute inter-set rest intervals. The protocol will adhere to the resistance training guidelines established by the American College of Sports Medicine (ACSM)
Study summary
To analyze the effect of 8 weeks of resistance training with blood flow restriction on muscle strength, clinical parameters, biochemical biomarkers, and perceived exertion in adults with obesity.
Eligibility
Sex
ALL
Min age
18 Years
Max age
30 Years
Healthy volunteers
No
Inclusion Criteria:
* Adults aged 18 to 40
* Both genders
* BMI ≥ 30 kg/m\^2 and \< 40 kg/m\^2
* Signed informed consent form
Exclusion Criteria:
* Participants who smoke
* Personal and family history of vascular disease or deep vein thrombosis
* Clinical diagnosis of hypothyroidism
* Clinical diagnosis of type 1 diabetes mellitus
* Clinical diagnosis of type 2 diabetes mellitus
* Clinical diagnosis of grade 3 obesity
* Clinical diagnosis of hypertension
* Clinical diagnosis of acute myocardial infarction or angina pectoris
* Use of nitrates and calcium channel blockers within 4 days prior to the start of the study
* Use of anticoagulants
* Use of beta-blockers or hypoglycemic agents within 7 days prior to the intervention
* Pregnant women
* Breastfeeding women
* Men consuming more than 40 g of alcohol per day or women consuming more than 20 g per day
* Postural and biomechanical disorders (knee, foot, and spine)
Primary outcome measure(s)
Muscle strength — Baseline and after 8 weeks Muscle strength (kg): Change from baseline to 8 weeks of intervention. Muscle strength will be assessed using dynamometry
Dynamic muscle strength — Baseline and after 8 weeks Dynamic muscle strength (kg): Change from baseline to 8 weeks of intervention.
Arm circumference — Baseline and after 8 weeks Arm circumference (cm): Change from baseline to 8 weeks of intervention. Measurements will be obtained using a non-elastic measuring tape in accordance with the International Society for the Advancement of Kinanthropometry (ISAK) protocol
Thigh circumference — Baseline and after 8 weeks Thigh circumference (cm): Change from baseline to 8 weeks of intervention. Measurements will be obtained using a non-elastic measuring tape in accordance with the International Society for the Advancement of Kinanthropometry (ISAK) protocol
Maximum oxygen uptake (VO₂max) — Baseline and after 8 weeks VO₂max (ml/min/kg): Change from Baseline at 8 weeks, measured using a submaximal exercise test based on the Åstrand-Ryhming protocol
Systolic blood pressure (SBP) — Baseline and after 8 weeks SBP (mmHg): Changes from baseline to 8 weeks of intervention
Diastolic blood pressure (DBP) — Baseline and after 8 weeks DBP (mmHg): Changes from baseline to 8 weeks of intervention
Heart rate — Baseline and after 8 weeks Heart rate (bpm): Change from baseline to 8 weeks of intervention.
Glucose — Baseline and after 8 weeks Glucose (mg/dl): Changes from baseline to 8 weeks of intervention
Triglycerides — Baseline and after 8 weeks Triglycerides (mg/dl): Changes from baseline to 8 weeks of intervention
Total cholesterol — Baseline and after 8 weeks Total cholesterol (mg/dl): Changes from baseline to 8 weeks of intervention
HDL cholesterol — Baseline and after 8 weeks HDL cholesterol (mg/dl): Changes from baseline to 8 weeks of intervention
LDL cholesterol — Baseline and after 8 weeks LDL cholesterol (mg/dl): Changes from baseline to 8 weeks of intervention
C-reactive protein (CRP) — Baseline and after 8 weeks CRP (mg/dl): Changes from baseline to 8 weeks of intervention
Interleukin-6 (IL-6) — Baseline and after 8 weeks IL-6 (pg/mL):Change from baseline to 8 weeks of intervention.
Tumor Necrosis Factor Alpha (TNF-α) — Baseline and after 8 weeks TNF-α (pg/mL): Change from baseline to 8 weeks of intervention
Weight — Baseline and after 8 weeks Weight (kg): Changes in weight from baseline to 8 weeks of intervention.
Height — Baseline and after 8 weeks Height (cm): Changes in height from baseline to 8 weeks of intervention
Body mass index (BMI) — Baseline and after 8 weeks BMI (kg/m\^2): Change from Baseline at 8 weeks, calculated by: weight (kg)/ height (m\^2).
Body fat percentage — Baseline and after 8 weeks Body fat percentage (%): Changes in body fat assessed by bioelectrical impedance analysis (BIA)
Muscle mass percentage — Baseline and after 8 weeks Muscle mass percentage (%): Changes in muscle mass measured using bioelectrical impedance analysis (BIA)
Perceived Exertion — Baseline and after 8 weeks Perceived exertion will be assessed using the Rating of Perceived Exertion Scale (RPE)
Exercise enjoyment — Baseline and after 8 weeks Exercise enjoyment will be assessed using the validated Physical Activity Enjoyment Scale Questionnaire (PACES)
Trial sites (1)
Facility
City
Region
Status
Centro Universitario de Tlajomulco
Tlajomulco de Zúñiga
Jalisco
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