Effects of Different Power Training Intensities in Older Adults

June 7, 2025 updated by: Antenor Barbosa Calandrini de Azevedo, Federal University of Rio Grande do Sul

Adaptations Due to Different Intensities of Power Training on Neuromuscular Performance, Muscle Thickness and Functional Capacity in Elderly People: A Randomized Clinical Trial

Power (strength × velocity) is a crucial component for maintaining independence during aging. Therefore, investigating interventions aimed at improving this physical capacity is essential for this population. The aim of this study is to examine the effects of power training (PT) performed at low to moderate intensity (PTLM; 40-60% of 1-repetition maximum [1RM]) and moderate to high intensity (PTMH; 65-80% of 1RM) on muscle power, kinematic gait parameters, strength, muscle thickness, and functional performance in older adults. Participants will be randomly assigned to perform PTLM and PTMH. Data collection will occur before and after familiarization, as well as at weeks 8 and 16 of the training programs. Participants will undergo a series of tests in the following sequence: 1) muscle thickness and 1RM test; 2) muscle power, maximum voluntary contraction, and rate of force development; 3) functional performance. The primary analyses will be conducted on an intention-to-treat basis, comparing the effects of the interventions and groups over time. Generalized Estimating Equations (GEE) will be used, considering the factors of group (2 levels) and time (3 levels). Paired comparisons will be assessed using the Bonferroni post-hoc test to identify significant differences between groups and time points. All tests will be performed using JASP software (version 0.16.4.0), with statistical significance set at p < 0.05 for all analyses.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

70

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • RS
      • Porto Alegre, RS, Brazil, 91410-070
        • Universidade Federal do Rio Grande do Sul (UFRGS)

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion criteria:

  • Age 60 years or older
  • No participation in regular and systematic resistance training in the last three months
  • No absolute or relative contraindications to exercise
  • No musculoskeletal injuries that could interfere with training and assessments

Exclusion criteria:

  • Use of steroids, nutritional supplements, or ergogenic substances
  • Failure to complete all study phases
  • Failure to complete more than 80% of the training sessions (32 sessions)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Low to moderate intensity (PTLM; 40-60% of 1-repetition maximum [1RM])
Power training performed at maximum velocity in the concentric phase with lower to moderate intensity
Power training performed at maximum velocity in the concentric phase with lower to moderate intensity
Other Names:
  • Ultrasound
  • Linear Encoder
  • Load Cell
  • 1-Repetition Maximum (1RM)
  • PTLM
Active Comparator: Moderate to high intensity (PTMH; 65-80% % of 1-repetition maximum [1RM])
Power training performed at maximum velocity in the concentric phase with moderate to high intensity
Power training performed at maximum velocity in the concentric phase with moderate to high intensity
Other Names:
  • Ultrasound
  • PTMH
  • Linear Encoder
  • Load Cell
  • 1-Repetition Maximum (1RM)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle Power
Time Frame: Pre- and post-intervention (16 weeks of training)

The power output during strength exercises is assessed using an encoder linear at two different intensities: 30% and 70% of 1RM in leg extension and leg press 45. Power output is the ability to generate force quickly and is a key measure of explosive strength. These tests are performed using different resistance levels to assess power across a range of intensities.

Measurement Tool: Encoder linear (linear encoder or velocity-based device)

Scale: Power output in watts (W)

Higher scores indicate better power performance at each intensity.

Pre- and post-intervention (16 weeks of training)
Muscle Strength
Time Frame: Pre- and post-intervention (16 weeks of training)

Muscle strength is the ability of a muscle or muscle group to generate force against resistance. It reflects the maximum force that can be produced in a single effort and is essential for daily activities and overall physical function. One Repetition Maximum (1RM) is used to quantify maximal strength.

Measurement Tool: 1RM testing

Scale: 1RM (measured in kg)

Higher scores indicate better strength performance.

Pre- and post-intervention (16 weeks of training)
Rate of Force Development
Time Frame: Pre- and post-intervention (16 weeks of training)

Rate of force development refers to the speed at which force is generated by a muscle or muscle group. It is a critical measure of neuromuscular performance, especially in activities that require explosive strength or rapid reactions. RFD is measured during maximal voluntary contractions.

Measurement Tool: Load Cell

Scale: Measured in Newtons per second (N/s)

Higher scores indicate better neuromuscular performance.

Pre- and post-intervention (16 weeks of training)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional Capacity
Time Frame: Pre- and post-intervention (16 weeks of training)

Functional capacity refers to an individual's ability to perform activities required for daily living, such as walking, climbing stairs, or carrying objects. It reflects overall physical function and is often used to assess health status, particularly in older adults or clinical populations. The following tests were selected to assess functional capacity:

Stair Climbing Test Scale: Total time to climb and descend a predetermined number of stairs. Shorter time indicates better performance. Timed Up and Go (TUG) Scale: Total time in seconds. Shorter time indicates better mobility and agility. 6-Meter Walk Speed Test Scale: Total time to walk 6 meters (seconds). Shorter time indicates faster walking speed. Sit-to-Stand Test (5 times) Scale: Total time to complete the 5 repetitions. Shorter time indicates better muscle strength and functional capacity.

Pre- and post-intervention (16 weeks of training)
Muscle hypertrophy
Time Frame: Pre- and post-intervention (16 weeks of training)

Muscle thickness is an indicator of muscle size and hypertrophy. It reflects the structural adaptations that occur in response to training. Ultrasound is used to measure the thickness of muscles such as the quadriceps, biceps, and triceps.

Measurement Tool: Ultrasound imaging

Scale: Muscle thickness in millimeters (mm)

Higher scores indicate greater muscle hypertrophy.

Pre- and post-intervention (16 weeks of training)
Cognitive Capacity
Time Frame: Pre- and post-intervention (16 weeks of training)

The Montreal Cognitive Assessment (MoCA) is a brief screening tool used to assess cognitive function. It evaluates multiple cognitive domains, including memory, attention, language, and executive functions. It is commonly used to assess cognitive decline or impairments.

Measurement Tool: MoCA test

Scale: MoCA score ranges from 0 to 30, with higher scores indicating better cognitive function.

Higher scores indicate better cognitive function.

Pre- and post-intervention (16 weeks of training)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 2, 2025

Primary Completion (Estimated)

December 11, 2025

Study Completion (Estimated)

December 11, 2025

Study Registration Dates

First Submitted

May 23, 2025

First Submitted That Met QC Criteria

June 7, 2025

First Posted (Actual)

June 15, 2025

Study Record Updates

Last Update Posted (Actual)

June 15, 2025

Last Update Submitted That Met QC Criteria

June 7, 2025

Last Verified

June 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 85503024.6.0000.5347

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Investigating the Effects of Power Training in the Elderly

Clinical Trials on low to moderate intensity (PTLM; 40-60% of 1-repetition maximum [1RM])

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