Effectiveness of iso-inertial resistance training on eccentric and concentric power, physical performance, and risk of falls in physically active middle-older adults: a randomised controlled trial

Abstract

Objective: To evaluate the effectiveness of iso-inertial resistance training on eccentric power compared to gravitational training in physically active middle-older adults. Methods: Parallel-group, randomised controlled trial at Espai Esport Wellness Center (Granollers, Spain). Forty-four physically active adults (>57 years of age) were randomised to iso-inertial (n=21) or gravitational (n=23) training groups (R software; 1:1 ratio). Participants had to complete a 6-week training program (2 sessions/week) consisting of three exercises (forward lunge, side lunge, forward lunge with row). Primary outcome: power in the eccentric phase of each exercise evaluated with both iso-inertial and gravitational devices. Secondary outcomes: concentric power, physical performance, risk of falls. Only outcome evaluators were blinded. We used multivariate linear regression models to analyse the effect of interventions. Results: Iso-inertial training showed better eccentric power gains than gravitational training for iso-inertial system evaluation, although the difference was only statistically significant for the side lunge. Forward lunge: between-group difference 3.99 W (95% CI: -3.99 to 11.33, p: 0.28); side lunge: difference 8.50 W (95% CI: 2.13 to 14.87; p: 0.01); forward lunge with row: difference 14.07 W (95% CI: -2.07 -to 30.20, p: 0.09). We observed no differences for the gravitational system evaluation nor for concentric power, physical performance, and risk of falls. The two groups improved remarkably from baseline for all outcomes. Conclusions: Iso-inertial resistance training might lead to better eccentric power gains than gravitational training. Both approaches seem equally effective in improving concentric power and physical performance, and reducing the risk of falls. Trial registration: ClinicalTrials.gov (NCT06160089).

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

NCT06160089

Funding Statement

This study did not receive any funding.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Drug Research Ethics Committee of the Universitat Internacional de Catalunya (Code: FIS-2023-03) gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

Data were stored and encoded in three Excel files to protect confidentiality before, during, and after the study. The first of these files contains the personal data of the participants (name and surnames, age, and sex), is accessible only to the administrative staff of the center, and served only to manage the recruitment of the participants. The second and third files are managed entirely by the research team and contain the registry of all the study outcomes. In these files, participants were identified by a code. Only the research team can relate the data collected in the study to the identity of the participants, which will not be available to anyone except in the event of a medical emergency or legal requirement. These two files have been shared in a public repository.

https://zenodo.org/records/11125189

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