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Velocity-Based Resistance Training Effects on Inflammation in Older Adults

Dose-Response Effects of Velocity-Based Resistance Training on Anti-Inflammatory Responses in Older Adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07566832
Enrollment
60
Registered
2026-05-05
Start date
2026-04-20
Completion date
2029-12-01
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Inflammatory Response

Brief summary

This study aims to investigate the effects of resistance training (RT) with different training volumes on immune modulation and anti-inflammatory responses in older adults. Participants will be randomly assigned to one of three RT volume groups (low, medium, or high) or a non-exercise control group. Participants in the training groups will complete a 4-week RT program, followed by a 4-week detraining phase. The findings are expected to provide evidence for volume-specific RT prescriptions to support healthy aging.

Interventions

OTHERResistance exercise

The RT program will consist of 12 sessions over a 4-week period, with participants training three times per week and at least one rest day between sessions. All sessions will be supervised by research personnel to ensure proper technique and safety. Exercises will be performed using resistance machines and will include chest press, shoulder press, seated row, lat pulldown, and leg press.

Sponsors

National Taipei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 60-75 years or older * No regular resistance training habit (defined as ≥2 sessions per week) in the past year * No musculoskeletal injuries within the past six months

Exclusion criteria

* Obesity (BMI \> 30 kg/m²), diabetes, hypertension, cancer, heart, kidney, or liver disease, or any other condition that may influence study outcomes. * Regular use of anti-inflammatory medications (e.g., NSAIDs). * Smoking or alcohol abuse * Inability to safely perform the prescribed resistance exercise movements * Unable to fully comprehend the study information and instructions.

Design outcomes

Primary

MeasureTime frameDescription
Changes in soluble IL-6 receptor concentrationBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingSoluble IL-6 receptor concentrations will be measured and reported in ng/mL.
Changes in soluble gp130 concentrationBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingSoluble gp130 concentrations will be measured and reported in ng/mL.
Changes in IL-10 concentrationBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIL-10 concentrations will be measured and reported in pg/mL.
Changes in IL-1RA concentrationBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIL-1RA concentrations will be measured and reported in pg/mL.
Changes in TNF-α concentrationBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingTNF-α concentrations will be measured and reported in pg/mL.
Changes in IL-6 concentrationBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingPlasma IL-6 concentrations will be measured and reported in pg/mL.

Secondary

MeasureTime frameDescription
Changes in monocyte countBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingMonocyte count will be measured and reported in cells/μL.
Body fat percentageBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingBody fat percentage will be measured using a body composition analyzer and reported as a percentage.
Lean body massBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingTotal lean body mass will be measured using a body composition analyzer and reported in kilograms.
Changes in gp130 (CD130) protein expression in PBMCsBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular gp130 (CD130) protein expression in PBMCs will be measured and reported in arbitrary units.
Changes in STAT3 protein expression in PBMCsBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular STAT3 protein expression in PBMCs will be measured and reported in arbitrary units.
Changes in phosphorylated STAT3 protein expression in PBMCsBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular phosphorylated STAT3 (p-STAT3) protein expression in PBMCs will be measured and reported in arbitrary units.
Borgs Ratings of Perceived Exertion (RPE)1-hour during each exercise interventionBorgs RPE is a method of estimating exertion rating, based on a 1 to 10 rating scale (1 being the no exertion at all, 10 being maximal exertion).
Handgrip strengthBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingMaximal handgrip strength will be assessed using a digital hand dynamometer and reported in kilograms.
Knee extension strengthBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingMaximal voluntary isometric and isokinetic concentric knee extension strength of the dominant leg will be assessed using an isokinetic dynamometer and reported in Newton-meters.
30-second chair-stand testBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingLower-body functional capacity will be assessed by the number of repetitions completed during a 30-second chair-stand test.
Single-leg balance testBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingBalance performance will be assessed as the duration of single-leg stance and reported in seconds.
Timed up and go testBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingFunctional mobility will be assessed using the Timed Up and Go test, with performance quantified as the time (seconds) required to stand up from a seated position, walk 3 meters, turn, walk back, and sit down.
Changes in IL-6 receptor alpha (CD126) protein expression in PBMCsBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular IL-6 receptor alpha (CD126) protein expression in PBMCs will be measured and reported in arbitrary units.
Changes in SHIP1 protein expression in peripheral blood mononuclear cells (PBMCs)Baseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular SHIP1 protein expression in PBMCs will be measured and reported in arbitrary units.
Changes in Beta-2 adrenergic receptor (β2-AR) protein expression in PBMCsBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular β2-adrenergic receptor (β2-AR) protein expression in PBMCs will be measured and reported in arbitrary units.
Changes in SOCS3 protein expression in PBMCsBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingIntracellular SOCS3 protein expression in PBMCs will be measured and reported in arbitrary units.
Changes in white blood cell countBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingTotal white blood cell count will be measured and reported in cells/μL.
Changes in lymphocyte countBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingLymphocyte count will be measured and reported in cells/μL.
Changes in neutrophil countBaseline, post-intervention (4 weeks), and at 2 and 4 weeks during detrainingNeutrophil count will be measured and reported in cells/μL.

Countries

Taiwan

Contacts

CONTACTShun-Hsi Tsai, Ph.D.
shunhsi@mail.ntpu.edu.tw+88686741111
PRINCIPAL_INVESTIGATORShun-Hsi Tsai, Ph.D.

National Taipei University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026