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Clinical Trials/NCT05859243
NCT05859243
Completed
Not Applicable

Effects of Traditional Concurrent Training and Concurrent Training Composed by Strenght Traning and Dance Classes in Functional Performance, Cognitive Function and Quality of Life of Older Adults: a Randomized Controlled Clinical Trial

Eduardo Lusa Cadore1 site in 1 country44 target enrollmentMay 22, 2023
ConditionsAging

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aging
Sponsor
Eduardo Lusa Cadore
Enrollment
44
Locations
1
Primary Endpoint
Change in Leg Strenght
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this randomized controlled clinical trial is to identify and compare the impacts of traditional concurrent training and concurrent training consisting of strength training combined with dance classes on functional performance, cognitive function and quality of life in older people. The main question it aims to answer are:

• The concurrent training consisting of strength training combined with dance classes can provide similar benefits to traditional concurrent training in neuromuscular and cardiorrespiratory performance, cognitive function and quality of life in older people?

Participants will training one of the two types of concurrent training (traditional concurrent training or concurrent training consisting of strength training combined with dance classes), two times a week, over 12 weeks.

Researchers will compare traditional concurrent training, concurrent training consisting of strength training combined with dance classes and a control group without exercise to see if this modalitys of physical exercise can provide increases in neuromuscular and cardiorrespiratory performance, cognitive function and quality of life in older people.

Registry
clinicaltrials.gov
Start Date
May 22, 2023
End Date
August 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Eduardo Lusa Cadore
Responsible Party
Sponsor Investigator
Principal Investigator

Eduardo Lusa Cadore

Professor

Federal University of Rio Grande do Sul

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in Leg Strenght

Time Frame: Baseline, 8 and 12 weeks

Assessed by One repetition maximum knee extension test

Change in Cognitive function

Time Frame: Baseline, 8 and 12 weeks

Assessed by Mini Exam of Mental State

Change in Static Balance

Time Frame: Baseline, 8 and 12 weeks

Assessed by One leg Stance Test

Change in Dynamic balance

Time Frame: Baseline, 8 and 12 weeks

Assessed by Timed Up and Go Test

Change in Self reported quality of life

Time Frame: Baseline, 8 and 12 weeks

Assessed by World Health Organization Quality of Life Questionary, on a scale ranging from 26 to 130. Higher scores are considered better.

Change in Leg Power

Time Frame: Baseline, 8 and 12 weeks

Assessd by 30% and 70% of One repetition maximum knee extension Test

Change in Seat to Stand Capacity

Time Frame: Baseline, 8 and 12 weeks

Assessed by 30s Seat to Stand Test

Change in Stairs Climb Capacity

Time Frame: Baseline, 8 and 12 weeks

Assessed by 10 step climb test

Change in Hand Grip Strenght

Time Frame: Baseline, 8 and 12 weeks

Assessed by Hand Grip Test with Hydraulic Dynamometer

Change in Cardiorrespiratory Capacity

Time Frame: Baseline, 8 and 12 weeks

Assessed by the 6 minutes walk test

Secondary Outcomes

  • Change in Affectivity with the intervention(8 and 12 weeks)
  • Change in Lipid profile(Baseline and 12 weeks)
  • Change in Quadriceps muscle thickness(Baseline and 12 weeks)
  • Change in Specific tension of quadriceps(Baseline and 12 weeks)
  • Change in depressive symptoms(Baseline and 12 weeks)

Study Sites (1)

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