Plyometric Exercise to Improve Rapid Force Production in Older Men

August 23, 2018 updated by: Evelien Van Roie, KU Leuven

Plyometric Exercise to Improve Rapid Force Production in Older Men: a Pilot Intervention

Rapid force production declines as a consequence of ageing. Given the functional relevance of rapid force production, exercise interventions in older adults should aim at improving the capacity to produce force rapidly. To improve this capacity, exercises should be performed with the intention to develop high speeds, as supported by previous work.

Human locomotion fundamentally consists of multi-joint movements and rapidly coupled eccentric-concentric muscle actions, known as stretch-shortening cycle (SSC) activities or plyometrics. Plyometrics might therefore be used to optimize power production. However, there is limited research on the feasibility of plyometrics in older adults and its potential effects on rapid force production and functional capacity. This study will test the feasibility of a 12-week plyometric exercise intervention in older men and compare its effects on rapid force production to a traditional resistance exercise or walking intervention.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

42

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

      • Leuven, Belgium, 3001
        • Department of Movement Sciences

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

65 years to 80 years (OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

-

Exclusion Criteria:

  • No systematic engagement in (resistance) exercise in the 12-months prior to participation
  • Cardiovascular disease
  • Neurological disorders
  • Cognitive malfunctioning
  • Severe knee or hip problems

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
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Plyometric exercise
12-week progressive exercise program, consisting of plyometric exercises such as countermovement jump, forward and sideways step-up.
12-week progressive training intervention
ACTIVE_COMPARATOR: Resistance exercise
12-week resistance exercise program for the leg muscles (2-4 sets of 8-15 repetitions at 8-15RM, leg press, leg extension, calve extension).
12-week progressive training intervention
ACTIVE_COMPARATOR: Walking
12-week progressive walking program.
12-week progressive training intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rapid force production
Time Frame: Change from baseline in rapid force production at 12 weeks
Subjects perform a test protocol on a sledge apparatus, consisting of explosive isometric voluntary contractions for the leg-extensor muscles of the right leg. The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). The knee joint angle is set at 90° and the hip angle at 70°. The point of force application is aligned with the head of the fifth metatarsal. Subjects are instructed to kick as fast and as hard as possible and maintain their maximum force for approximately 3s. The rate of force development (N/s) is defined as the linear slope of the force-time curve and is measured from the onset of movement till 100 ms.
Change from baseline in rapid force production at 12 weeks
Jumping height in squat jump
Time Frame: Change from baseline in jumping height at 12 weeks
Subjects perform a test protocol on a sledge apparatus, consisting of squat jumps (SJ), countermovement jumps (CMJ), and drop jumps (DJ). The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). A force platform is built in perpendicular to the jumping direction. A speed sensor is attached to the seat of the sledge, which is used to assess the transition point between braking and push-off phases and to calculate jumping height (in cm).
Change from baseline in jumping height at 12 weeks
Jumping height in countermovement jump
Time Frame: Change from baseline in jumping height at 12 weeks
Subjects perform a test protocol on a sledge apparatus, consisting of squat jumps (SJ), countermovement jumps (CMJ), and drop jumps (DJ). The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). A force platform is built in perpendicular to the jumping direction. A speed sensor is attached to the seat of the sledge, which is used to assess the transition point between braking and push-off phases and to calculate jumping height (in cm).
Change from baseline in jumping height at 12 weeks
Jumping height in drop jump
Time Frame: Change from baseline in jumping height at 12 weeks
Subjects perform a test protocol on a sledge apparatus, consisting of squat jumps (SJ), countermovement jumps (CMJ), and drop jumps (DJ). The inclination of the sledge is 20° to horizontal. The seat of the sledge is inclined backwards (130°). A force platform is built in perpendicular to the jumping direction. A speed sensor is attached to the seat of the sledge, which is used to assess the transition point between braking and push-off phases and to calculate jumping height (in cm).
Change from baseline in jumping height at 12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Leg press one-repetition maximum
Time Frame: Change from baseline in leg press 1-RM at 12 weeks
Leg press one-repetition maximum is defined as the maximum weight (in kg) that the subject can push on a leg press device (Signature Series Leg press Life Fitness).
Change from baseline in leg press 1-RM at 12 weeks
Maximal isometric strength
Time Frame: Change from baseline in maximal isometric strength at 12 weeks
Maximal strength (Nm) is measured by means of unilateral isometric knee-extensor tests on a Biodex dynamometer.
Change from baseline in maximal isometric strength at 12 weeks
Maximal isokinetic strength
Time Frame: Change from baseline in maximal isokinetic strength at 12 weeks
Maximal strength (Nm) is measured by means of unilateral isokinetic knee-extensor tests on a Biodex dynamometer.
Change from baseline in maximal isokinetic strength at 12 weeks
Stair Climbing performance
Time Frame: Change from baseline in Stair Climbing performance at 12 weeks
Stair ascent duration (in s), the time needed to ascent a flight of stairs.
Change from baseline in Stair Climbing performance at 12 weeks
Gait speed
Time Frame: Change from baseline in gait speed at 12 weeks
The average speed to walk 10m as fast as possible (in m/s).
Change from baseline in gait speed at 12 weeks
5 repetition sit-to-stand test
Time Frame: Change from baseline in sit-to-stand duration at 12 weeks
The time needed to perform 5 sit-to-stand transitions (in s).
Change from baseline in sit-to-stand duration at 12 weeks
6 minute walk distance
Time Frame: Change from baseline in 6min walk distance at 12 weeks
The walk distance (in m) covered in 6 min.
Change from baseline in 6min walk distance at 12 weeks
Balance
Time Frame: Change from baseline in balance at 12 weeks
Overall balance performance is assessed using the total length of the sway path divided by duration of the measurement (mm/s) in a 30s balance test on a balance board.
Change from baseline in balance at 12 weeks

Collaborators and Investigators

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

Sponsor

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)

January 29, 2018

Primary Completion (ACTUAL)

June 19, 2018

Study Completion (ACTUAL)

June 19, 2018

Study Registration Dates

First Submitted

August 17, 2018

First Submitted That Met QC Criteria

August 23, 2018

First Posted (ACTUAL)

August 24, 2018

Study Record Updates

Last Update Posted (ACTUAL)

August 24, 2018

Last Update Submitted That Met QC Criteria

August 23, 2018

Last Verified

August 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • S60983

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.

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