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AgingNCT03206580

Functional Mobility in the Elderly: Influence of Morphological, Neuromuscular and Training Parameters

A study testing Concentric training and Concentric-Eccentric training in people with Aging, run by Federal University of Rio Grande do Sul at 1 site in Brazil.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Life expectancy and elderly population are increasing. Health professionals try to provide longevity with good quality of life for this population, through the functional independence maintenance. In this context, physical exercise has an important role, specially the strength training. Read more about this study

Who is it for?
Ages 65 to 85 years, men onlyHealthy volunteers can take part
Conditions the study is for
Aging
What is being tested?
Concentric training and Concentric-Eccentric training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
11 participants
Where
1 siteBrazil
Study dates
15 Oct 2016to 31 Dec 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 65 to 85 years
  • Men only
  • Healthy volunteers accepted
  • Older adult

Who may be able to join

  • Male;
  • 65 years of age or more;
  • able to walk independently;
  • not engaged in regular physical exercise.

Who cannot join

  • Auditory, vestibular, visual and/or neuromusculoskeletal impairments that could influence the tests and the training;
  • severe cognitive impairment;
  • lower limb surgery;
  • osteoporosis;
  • lower limb pain.

Trial locations and contacts

1 site in 1 country.

Brazil1 site
  • Exercise Research Laboratory, School of Physical Education, Federal University of Rio Grande do Sul

    Porto Alegre, Rio Grande do Sul, 90690-200

Other trials in Brazil

About this study

Official title: Functional Mobility in the Elderly: Influence of Morphological, Neuromuscular and Training

Life expectancy and elderly population are increasing. Health professionals try to provide longevity with good quality of life for this population, through the functional independence maintenance. In this context, physical exercise has an important role, specially the strength training. The ability to produce muscle strength is positively associated with the functionality and independence of older people. Different types of strength training can lead to different neuromuscular and functional gains. These types of interventions can help health professionals to determine characteristics of training for the elderly, aiming the maintenance of their functional independence. Thus, the purpose of this study is to determine the effects of a concentric strength training versus a concentric-eccentric strength training for knee flexors and extensors on structural, neuromuscular and functional parameters in older people, as well as to investigate the effect of a detraining period. Additionally, the investigators will try to identify which structural and neuromuscular parameters of lower limbs are better related to the functionality.

Conditions
Aging
Being tested
Concentric training, Concentric-Eccentric training
Keywords
aging, strength training, functionality

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Concentric trainingOther

    Subjects will be submitted to 8 weeks (16 sessions) of a concentric training for knee flexors and knee extensors. This training will be performed in an isokinetic dynamometer at 70% of the subject's maximal voluntary isometric contraction.

  • Concentric-Eccentric trainingOther

    Subjects will be submitted to 8 weeks (16 sessions) of a concentric-eccentric training for knee flexors and knee extensors. This training will be performed in an isokinetic dynamometer at 70% of the subject's maximal voluntary isometric contraction.

Study groups in NCT03206580
Study groupRoleWhat they receive
Concentric trainingExperimentalConcentric training
Receives: Other: Concentric training
Concentric-eccentric trainingExperimentalConcentric-eccentric training
Receives: Other: Concentric-Eccentric training

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pennation angle of rectus femoris, vastus lateralis and biceps femoris, bilaterally.

    Pennation angle at rest

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  2. Thickness of rectus femoris, vastus lateralis and biceps femoris, bilaterally.

    Muscle thickness at rest

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  3. Fascicle length of rectus femoris, vastus lateralis and biceps femoris, bilaterally.

    Fascicle length at rest

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  4. Echo intensity of rectus femoris, vastus lateralis and biceps femoris, bilaterally.

    Echo intensity determined from a gray scale analysis of the muscles at rest

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  5. Countermovement vertical jump

    Maximal vertical height in the countermovement jump

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  6. Timed-up-&-go

    Time to rise from a chair, walk 3 meters, turn, walk back and sit again

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  7. Unipodal static balance

    Range in anterior-posterior and medio-lateral center of pressure movement during unipodal evaluation during 30 seconds

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  8. Gait speed

    Gait speed for walking 10 meters at self-selected speed

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  9. Stair ascent and descent time

    Time to stair ascent and descent stairs

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  10. 6-minutes walking test

    The distance that the subjects can walk during 6 minutes

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  11. Sit-to-stand

    Maximal number of repetitions during 30 seconds

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  12. Power of knee extensors and knee flexors

    Power during maximal concentric and eccentric contractions

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  13. Rate of torque production of knee extensors and knee flexors

    Rate of torque production during maximal isometric contractions

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  14. Strength of knee extensors and knee flexors

    Maximal isometric strength

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  15. Strength of knee extensors and knee flexors

    Maximal concentric strength

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

  16. Strength of knee extensors and knee flexors

    Maximal eccentric strength

    Measured: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Jul 2017
  2. Study start15 Oct 2016
  3. Primary completion31 Dec 2018
  4. Study completion31 Dec 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
11 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03206580
Sponsor's protocol ID
UFRGS 2.034.508
Status last verified
Jun 2024
First submitted
22 Jun 2017
Last updated
10 Jun 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Concentric training and Concentric-Eccentric training in people with Aging, run by Federal University of Rio Grande do Sul at 1 site in Brazil.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pennation angle of rectus femoris, vastus lateralis and biceps femoris, bilaterally. (time frame: First evaluation, change from first evaluation to baseline, change from baseline to 8 weeks of training, change from 8 weeks of training to 4 weeks of detraining and change from 4 weeks of detraining to 8 weeks of detraining). The study lists 16 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jun 2024.

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