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Completed

NCT Number: NCT05859243

Effects of Two Types of Concurrent Training in Functional Performance and Cognitive Function of Older Adults

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.

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Key information

Age range

65 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Escola de Educação Física, Fisioterapia e Dança - UFRGS

Porto Alegre, Rio Grande do Sul, 90690-200, Brazil

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be male or female aged between 65 and 75 years old
  • Do not practice regular physical exercises for at least three months
  • No history of competitive sports throughout life
  • Not having musculoskeletal and neurological diseases or disorders that may influence the performance of the exercises or affect the test results
  • Not having health conditions in which physical exercise is contraindicated
  • Achieve a score of no less than 24 on the Mini Mental State Exam
  • Achieve a score of up to 9.11 on the Baecke Physical Activity Questionnaire.

Exclusion criteria

  • Miss more than 20% of training sessions
  • Miss more than three workouts in a row
  • Failure to attend any of the evaluations will be excluded from the study.

Treatment and study plan

Traditional concurrent training

Behavioral

The subjects will perform two sessions per week of traditional concurrent training, consisting of strength training followed by aerobic exercise over 12 weeks, with progressive intensities and training volumes. Each traditional concurrent training session will consist of specific warm-up performed on equipment for upper and lower limbs with a load of less than 30% of the training load. Then the bench press, low row, leg press, extension and knee flexion exercises will be performed. Participants will be instructed to perform the concentric phase of the movement in one second and the eccentric phase in two seconds. After strength training, aerobic training (walking outdoors or on a treadmill) will be performed with intensity based on the adapted BORG effort perception scale (ranged to 0 = minimum effort, to 10 = maximal effort).

Concurrent training consisting of strength training combined with dance classes

Behavioral

Each concurrent training session associated with dance classes will consist of the same strength training as the traditional concurrent training group, but the traditional aerobic training will be replaced by a dance class. Each dance class will consist of a 5-minute general warm-up with joint mobility exercises and dynamic stretching. Then the main part will be performed with the elaboration of choreography, lasting approximately 20 minutes. Finally, there will be a 5-minute cool-down with stretching exercises. Classes will be held in four different dance modalities, divided into four modules.

Primary outcomes

  1. Change in Dynamic balance

    Time frame: Baseline, 8 and 12 weeks

    Assessed by Timed Up and Go Test

  2. Change in Cognitive function

    Time frame: Baseline, 8 and 12 weeks

    Assessed by Mini Exam of Mental State

  3. 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.

  4. Change in Static Balance

    Time frame: Baseline, 8 and 12 weeks

    Assessed by One leg Stance Test

  5. Change in Seat to Stand Capacity

    Time frame: Baseline, 8 and 12 weeks

    Assessed by 30s Seat to Stand Test

  6. Change in Stairs Climb Capacity

    Time frame: Baseline, 8 and 12 weeks

    Assessed by 10 step climb test

  7. Change in Leg Strenght

    Time frame: Baseline, 8 and 12 weeks

    Assessed by One repetition maximum knee extension test

  8. Change in Leg Power

    Time frame: Baseline, 8 and 12 weeks

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

  9. Change in Hand Grip Strenght

    Time frame: Baseline, 8 and 12 weeks

    Assessed by Hand Grip Test with Hydraulic Dynamometer

  10. Change in Cardiorrespiratory Capacity

    Time frame: Baseline, 8 and 12 weeks

    Assessed by the 6 minutes walk test

Secondary outcomes

  1. Change in Quadriceps muscle thickness

    Time frame: Baseline and 12 weeks

    Assessed by ultrasound

  2. Change in Affectivity with the intervention

    Time frame: 8 and 12 weeks

    Assessed by Scale (+5 = very good, -5 = very bad)

  3. Change in Lipid profile

    Time frame: Baseline and 12 weeks

    plasma concentrations of total cholesterol, HDL and triglycerides will be determined by the colorimetric method with specific kits in an automatic analyzer (Cobas C111, Roche Diagnostics, Basel, Switzerland).

  4. Change in Specific tension of quadriceps

    Time frame: Baseline and 12 weeks

    Calculated by the formula: maximum knee extension strength/quadriceps muscle thickness

  5. Change in depressive symptoms

    Time frame: Baseline and 12 weeks

    Measured using the Geriatric Depression Scale, that consists of 15 questions with binary answers (yes/no) and easy to understand. It ranges from zero (absence of depressive symptoms) to fifteen points (maximum score of depressive symptoms).

Sponsors and collaborators

Lead sponsor

Eduardo Lusa Cadore

Other

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
May 15, 2023
Registry last updated
Apr 1, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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