Flywheel Resistance Training and Traditional Resistance Training in Older Women With Sedentary Behaviors
NCT ID: NCT06758206
Last Updated: 2026-01-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
64 participants
INTERVENTIONAL
2025-03-10
2026-01-21
Brief Summary
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To date, evidence from randomized clinical trials has compared the effectiveness of aerobic, resistance, and Pilates exercises in reducing depressive symptoms and improving physical and executive function in older women.
While experimental studies have demonstrated the efficacy of physical exercise, the effect of long-term eccentrically reinforced resistance training on depressive symptoms, physical function, and executive function in sedentary older women remains unclear.
Therefore, this study aims to evaluate the safety and effect of eccentrically reinforced resistance exercise versus traditional resistance training on depressive symptoms, physical and executive function, quality of life, different manifestations of muscle strength, body composition, vital signs, abdominal circumference, fall risk, and fatigue symptoms in sedentary older women over a 10-month period.
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Detailed Description
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Participants will be assessed at three time points during the training program: pre-intervention, 5 months, and 10 months after the intervention starts. Lower limb muscle strength will be evaluated using one-repetition maximum (1RM) tests on a knee extension machine and through maximal voluntary isometric contraction (MVIC), assessed with a load cell. Depressive symptoms will be measured using the Geriatric Depression Scale (GDS), validated for use in Brazil. Physical function will be assessed through the Timed Up and Go (TUG) test and the Senior Fitness Test (SFT). Executive function will be evaluated using the Victoria Stroop test, Digit Span (forward and backward), and the Trail Making Test (parts A and B). Quality of life will be assessed using the Brazilian version of the WHOQOL-Bref, while body composition will be analyzed through dual-energy X-ray absorptiometry (DXA). Blood pressure (systolic, diastolic, and mean arterial pressure) will be measured using an aneroid sphygmomanometer, and resting heart rate will be manually recorded after 3 minutes in a seated position. Abdominal circumference will be measured with a metal tape at the midpoint between the lower costal margin and the iliac crest, at the end of a normal expiration. Fall risk will be assessed using the Falls Efficacy Scale-International (FES-I) and the Berg Balance Scale. Fatigue symptoms will be evaluated using the Fatigue Symptom Inventory (FSI).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Flywheel resistance training
Flywheel resistance training will use the isoinertial multi-leg machine for lower and upper limbs for women.
Flywheel Resistance Training
For each training session, 6 to 7 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps extension, seated row, shoulder flexion and shoulder raise). They will perform 4 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
Traditional resistance training
Traditional resistance training will use machines for the lower limbs and free weights for the upper limbs.
Traditional resistance training
For each training session, 6 to 7 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps extension, seated row, shoulder flexion and shoulder raise). They will perform 4 sets of 8 to 12 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at moderate and high intensities (6 to 10 on the OMNI-RES scale).
Interventions
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Flywheel Resistance Training
For each training session, 6 to 7 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps extension, seated row, shoulder flexion and shoulder raise). They will perform 4 sets of 8 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at a high intensity (always 10 on the OMNI-RES Scale).
Traditional resistance training
For each training session, 6 to 7 generic exercises will be performed, involving small and large muscle groups (leg extension, leg flexion, biceps curl, triceps extension, seated row, shoulder flexion and shoulder raise). They will perform 4 sets of 8 to 12 repetitions, with a 2-minute break between exercises and sets. They will perform these exercises at moderate and high intensities (6 to 10 on the OMNI-RES scale).
Eligibility Criteria
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Inclusion Criteria
* Self-reported proficiency in speaking, writing, and understanding Portuguese.
* Willingness and availability to participate in all trial procedures.
* Good vision in at least one eye.
* Absence of any medical contraindications for engaging in physical exercise.
* Engage in less than 150 minutes of physical activity per week.
* Not clinical diagnosis of major depressive disorder at the time of the interventions.
Exclusion Criteria
* Surgical procedures scheduled during the intervention period.
* Diagnosis of joint diseases such as osteoarthritis and arthrosis.
* Participating in aerobic or resistance exercise programs twice a week for the past three months.
60 Years
FEMALE
Yes
Sponsors
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Federal University of Vicosa
OTHER
Responsible Party
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Pablo Augusto Garcia Agostinho
Ph.D. Student in Physical Education, Principal Investigator
Principal Investigators
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Osvaldo Costa Moreira
Role: STUDY_DIRECTOR
Federal University Of Viçosa
Edison A Pérez Bedoya
Role: STUDY_DIRECTOR
Antioquia University
Locations
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Universidade Federal de Viçosa
Viçosa, Minas Gerais, Brazil
Federal University of Viçosa, Viçosa - Minas Gerais
Viçosa, Minas Gerais, Brazil
Countries
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Other Identifiers
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1.821.139
Identifier Type: -
Identifier Source: org_study_id
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