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Enrolling by invitation Not applicable

Effects of Eccentric Training at Long Muscle Length on Functional Capacities of Elderly Adults

NCT06953258 · tracked via the Priya Life Science France tracker
Sponsor
Robin Souron
Phase
Not applicable
Started
2025-09-01
Last updated
2025-05-01

Condition(s) studied

Eccentric ExerciseHome-based TrainingElderly Adults

Investigational drug(s) / intervention(s)

Home-based eccentric training at long muscle lengthConventional home-based training

Home-based eccentric training at long muscle length: The training program will include conventional resistance exercises, with progressive increases in intensity and volume tailored to each participant's capabilities. In this condition, specific to the Arm #1, four specific exercises targeting the knee extensors and plantar flexors will be performed at long muscle lengths.

Conventional home-based training: The training program will include conventional resistance exercises, with progressive increases in intensity and volume tailored to each participant's capabilities. In this condition, specific to the Arm#2, four specific exercises targeting the knee extensors and plantar flexors will be performed in a conventional manner (i.e., at neutral or shorter muscle lengths).

Study summary

As aging leads to a decline in muscle function and overall physical performance, interventions targeting muscle strength and neuromechanical properties are critical for maintaining functional independence in older adults. Long-length eccentric training has shown promise in enhancing muscle performance, but its effects in older adults, particularly in a home-based setting, remain underexplored.

The aim of this trial is to assess whether a targeted home-based training intervention incorporating long-length eccentric contractions can enhance functional capacity and neuromechanical properties in healthy older adults. Participants will be semi-randomly allocated to one of two groups: an experimental group incorporating long-length eccentric contractions (Group 1) or a conventional resistance training group (Group 2), with group assignment stratified to ensure an equal number of men and women in each group. Each participant will complete three laboratory-based experimental sessions (i.e., two Pre-training sessions and one Post-training session) , during which five key evaluations will be conducted: (i) the 5-Time Sit to Stand test, serving as the primary outcome measure; (ii) the Timed Up and Go test; (iii) assessments of isometric and dynamic muscle strength in the knee extensors and plantar flexors; (iv) measurements of the cross-sectional areas of the vastus lateralis, rectus femoris, gastrocnemius medialis, and soleus muscles; and (v) evaluation of tendon stiffness.

Following the pre-evaluation, each participant will engage in a 24-session, semi-supervised, home-based training protocol over a period of 8 to 11 weeks. The training program will include eight exercises, with four targeting the upper limbs and four focused on the lower limbs. Group 1 will perform the lower limb exercises at long muscle lengths, while Group 2 will perform the same exercises in a conventional manner (i.e., at neutral or shorter muscle lengths). The total training volume (calculated as repetitions × sets, in arbitrary units) will be matched across both groups, ensuring that any observed differences in outcomes are attributable to the specific training modality rather than differences in workload.

Eligibility

Sex
ALL
Min age
60 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Men or women 60 years and older * Individuals eligible for social security coverage * Individuals without health issues (e.g., musculoskeletal injuries, chronic conditions) * Individuals who have given their informed consent Exclusion Criteria: * Accustomed to resistance exercise (i.e., no participation in a resistance training program within the 6 months prior to enrollment, or not engaging in lower-limb resistance training more than once per week as part of their current routine). * Pathologies affecting muscle strength in the lower limbs (e.g., neurological or neuromuscular conditions, history of ankle or knee trauma) * Individuals residing in a healthcare or social institution * Individuals receiving psychiatric care * Individuals deprived of their liberty * Adults under legal protection (guardianship, curatorship, or legal safeguard) * Participation in another ongoing biomedical research study * Individuals in an emergency situation * Individuals not covered by social security * BMI over 30 * Minimal Mental State Examination (MMSE) score of 25 or lower * Significant visual impairment

Primary outcome measure(s)

  • 5 times Sit to Stand — At baseline (i.e., prior to the start of training) and at study completion (i.e., within one week following the final training session
    The subjects will complete five times STS repetitions on a standardized armless chair. After the cue "ready, set, go!", the subjects will start performing STS repetitions as rapidly as possible from the sitting position with their buttocks touching the chair to the full standing position, with their arms crossed over the chest. Verbal encouragement will be given during the test. The STS test will finish when the subjects sit on the chair after the fifth STS repetition, and the time needed to complete the task will be recorded with a stopwatch to the nearest 0.01 s.

Trial sites (1)

FacilityCityRegionStatus
MIP Laboratory, Nantes University Nantes France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06953258 on ClinicalTrials.gov ↗ ← All trials in France