Aging Clinical Trial
Official 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
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.
Status | Recruiting |
Enrollment | 36 |
Est. completion date | August 30, 2024 |
Est. primary completion date | August 30, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 65 Years to 75 Years |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
Brazil | Escola de Educação Física, Fisioterapia e Dança - UFRGS | Porto Alegre | Rio Grande Do Sul |
Lead Sponsor | Collaborator |
---|---|
Eduardo Lusa Cadore |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Dynamic balance | Assessed by Timed Up and Go Test | Baseline, 8 and 12 weeks | |
Primary | Change in Cognitive function | Assessed by Mini Exam of Mental State | Baseline, 8 and 12 weeks | |
Primary | Change in Self reported quality of life | Assessed by World Health Organization Quality of Life Questionary, on a scale ranging from 26 to 130. Higher scores are considered better. | Baseline, 8 and 12 weeks | |
Primary | Change in Static Balance | Assessed by One leg Stance Test | Baseline, 8 and 12 weeks | |
Primary | Change in Seat to Stand Capacity | Assessed by 30s Seat to Stand Test | Baseline, 8 and 12 weeks | |
Primary | Change in Stairs Climb Capacity | Assessed by 10 step climb test | Baseline, 8 and 12 weeks | |
Primary | Change in Leg Strenght | Assessed by One repetition maximum knee extension test | Baseline, 8 and 12 weeks | |
Primary | Change in Leg Power | Assessd by 30% and 70% of One repetition maximum knee extension Test | Baseline, 8 and 12 weeks | |
Primary | Change in Hand Grip Strenght | Assessed by Hand Grip Test with Hydraulic Dynamometer | Baseline, 8 and 12 weeks | |
Primary | Change in Cardiorrespiratory Capacity | Assessed by the 6 minutes walk test | Baseline, 8 and 12 weeks | |
Secondary | Change in Quadriceps muscle thickness | Assessed by ultrasound | Baseline and 12 weeks | |
Secondary | Change in Affectivity with the intervention | Assessed by Scale (+5 = very good, -5 = very bad) | 8 and 12 weeks | |
Secondary | Change in Lipid profile | 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). | Baseline and 12 weeks | |
Secondary | Change in Specific tension of quadriceps | Calculated by the formula: maximum knee extension strength/quadriceps muscle thickness | Baseline and 12 weeks | |
Secondary | Change in depressive symptoms | 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). | Baseline and 12 weeks |
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