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Effects of Training on Outdoor Fitness Equipment for Health Improvement

Design and Development of a New Line of Outdoor Fitness Equipment: BIOFIT-Park A Study on Ergonomics, Safety and Efficiency

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05331794
Enrollment
70
Registered
2022-04-18
Start date
2022-06-01
Completion date
2022-07-31
Last updated
2024-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy, Physical Inactivity

Keywords

Outdoor fitness equipment, Outdoor gym, Physical fitness

Brief summary

Aging causes various changes in the body. This, together with a sedentary lifestyle, can lead to health problems such as loss of muscle mass and strength, bone mineral density and cardiovascular capacity. Therefore, it is essential to remain physically active in adulthood. Outdoor fitness equipment offer a free and easy-to-use option for physical activity and health improvement. However, there are few studies that quantitatively evaluate the physical fitness and health improvement associated with the use of these parks. Hence, the main objective is: 1) To evaluate the effects of training on outdoor fitness equipment on different body composition and health-related fitness parameters.

Detailed description

Physiological, psychological and functional deterioration is associated with the aging process. It has been demonstrated that the practice of physical activity can prevent, slow or reduce this deterioration. Bio-healthy parks are an alternative for practicing physical activity outdoors and free of charge. However, there is no research that analyzes the effect of a planned training program in these parks. Therefore, the objectives of this project are 1) To evaluate the effects of training on outdoor fitness equipment on different body composition and health-related fitness parameters. The present project will be developed through a randomized controlled trial, with 1 experimental and 1 control group, with pre-test and post-test, with intra-group and inter-group analysis for each of the dependent variables of the study. The inclusion criteria are: (a) not having participated in a structured exercise program for at least 1 year, (b) being older than 50 years of age, and (c) being physically independent. The exclusion criteria are: (a) having musculoskeletal injuries or limitations that could affect the health and physical performance of the person; (b) being under medical prescription for taking medications that could influence physical performance; (c) not regularly attending the proposed sessions. Body composition and bone mineral density will be assessed by dual energy X-ray absorptiometry (DEXA). Blood pressure by means of an automatic device (Colin BP 880, Inc., Tampa, FL). Strength by manual dynamometry (TKK 5401; Co., Ltd., Tokyo, Japan) and maximal isometric strength of knee extension and biceps flexion. Functional capacity will be assessed by means of the Chari stand test, gait speed, time up and go test and Short physical performance battery (SPPB), Sarcopenia will be assessed taking into account the reference values established for muscle quality (hand grip strength and chair stand test), muscle quantity (DEXA fat-free mass) and functional competence (gait speed, time up and go test, SPPB and 400 meter walk) established by the European Consensus (EWGSOP2). The Spinal Mouse device (Switzerland) will be used to assess the sagittal disposition of the spine (thoracic curve, lumbar curve and pelvic tilt) in standing and relaxed sitting. This technique is non-invasive. Health-related quality of life and satisfaction with life will be assessed by means of the SF36 and The Satisfaction with Life Scale (SWL) questionnaires. Mediterranean diet adherence will be assess with a Mediterranean diet adherence questionaire. Experimental group 1 will receive the exercise program on bio-healthy machinery with a frequency of 2 sessions per week of 55 minutes for 8 weeks. The machines used will be rider, low gemini, high gemini, walk, bottoms, flywheels circles, flywheels rotation, twin swing, surf, swing press and rowing. Intensity will be controlled by subjective perception of effort and heart rate (Polar 420). There will be a warm-up 8-10 minutes, a main part 40-45 minutes and a return to calm 5-10 minutes. The intervention programs will be developed by a graduate in Physical Activity and Sport Sciences. The load will be progressed every 2 weeks. The control group will not perform any intervention program following their usual activity.

Interventions

BEHAVIORALTraining on BIOFIT-Park

Participant will perform one strength training session on the new line of outdoor fitness equipment BIOFIT-Park. 6 machines will be used. The training will consist of 3 sets of 15-20 repetitions, working at 60-65% RM. The execution speed will be 1x1, the rest between machines will be 20 seconds and macropauses of 90 seconds between series.

BEHAVIORALTraining on gym park equipament

Participant will perform one strength training session on a gym park equipment. 6 machines will be used. The training will consist of 3 sets of 15-20 repetitions, working at 60-65% RM. The execution speed will be 1x1, the rest between machines will be 20 seconds and macropauses of 90 seconds between series.

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Not present any surgery, pathology or condition that prevents the practice of physical activity or may interfere with the results of the tests. * Do not present any acute infection in the last 2 weeks. * Do not having carried out physical exercise similar to that performed during intervention.

Exclusion criteria

* Have answered yes to any of the items of the Physical Activity Readiness Questionnaire (PAR-Q). * Have a medical contraindication to exercise. * Failure to complete or attend training or measurements sessions during the intervention. * Practice regular physical exercise outside the intervention or change habits that may influence the tests.

Design outcomes

Primary

MeasureTime frameDescription
Subjective perception of effortDuring exerciseEvaluation of subjective perception of effort by ONMI-RES scale. The scale goes from 1 to 10 and the subject reports on his subjective perception of effort, with 1 being the lowest value and 10 the highest value.
Knee Extension Strength TestPre-test and post-testEvaluation of the maximum voluntary contraction (MVC) of the quadriceps through a dynamometer on a seated leg extension machine.
Arm Curl Strength TestPre-test and post-testEvaluation of the maximum voluntary contraction (MVC) of the elbow flexor muscles through a dynamometer in standing position.
Lactate Blood TestPre-test and post-testEvaluation of serum lactate level (mmol/L) through a finger pick method
Excess Post-Exercise Oxygen Consumption TestPost-testEvaluation of excess post-exercise oxygen consumption (EPOC) during the minutes following exercise sessions through indirect calorimetry.
Energy expenditureDuring exerciseEvaluation of energy expenditure of participants during exercise through indirect calorimetry
Heart rateDuring exerciseEvaluation of heart rate measured via a heart rate monitor band.
Rest Metabolic RatePre-testEvaluation of resting metabolic rate through an indirect calorimetry test.
Heart Rate VariabilityPre-test and post-testEvaluation of changes in heart rate variability index measured via a heart rate monitor band.
Blood PressurePre-test and post-testNon-invasive evaluation of systolic and diastolic peripheral blood pressure changes.
Counter Movement Jump TestPre-test and post-testEvaluation of explosive force in lower limb through vertical jump height in centimetres.
Knee Extension Rate of Foce Development Strength TestPre-test and post-testEvaluation of force production capacity per unit time through a dynamometer on a seated leg extension machine.

Secondary

MeasureTime frameDescription
Global Physical Activity QuestionnairePre-testQuestionnaire to evaluate the level of physical activity performed in the daily routine. The questionnaire collects information on the time in minutes and frequency per week of moderate and vigorous physical activity, walking and sedentary activities. A greater time of physical activity and walking; and less time spent in sedentary activities would be considered a better score.
Dietary Recall QuestionnairePre-test24-hour pre-intervention dietary intake recording instrument.
HeightPre-testHeight will be assessed following the methodology proposed by the International Society for the Advancement of Kinathropometry (ISAK). The values will be expressed in meters.
Weight and bone weightPre-testWeight and bone weight will be performance with BIA-derived body composition measurements. It will be reported as a kilograms.
Percentaje of fat, hydration and muscle mass.Pre-testAverage of fat, hydration and muscle mass will be performance with BIA-derived body composition measurements. It will be reported as a percentaje.
Sociodemographic questionnairePre-testTo define individual characteristics of participants such as age, gender or ethnicity.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026