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Prescription of Physical Exercise Through Mobile Application in Elderly

Effects of a Training Program of Physical Exercise Administered Through Mobile Application in Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02327975
Acronym
PEME
Enrollment
48
Registered
2014-12-31
Start date
2012-11-30
Completion date
Unknown
Last updated
2015-03-03

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

Conditions

Aerobic Exercise, Aged, Cell Phones, Mobile Applications, Motor Activity, Muscle Strenght, Prescriptions, Resistance Training

Brief summary

Physical inactivity is a health problem that affects people worldwide and has been identified as the fourth largest risk factor for overall mortality (contributing to 6% of deaths globally). Many researchers have tried to increase physical activity (PA) levels through traditional methods without much success. Thus, many researchers are turning to mobile technology as an emerging method for changing health behaviours.The study consists of a physical activity intervention through a mobile application in elderly. The study is a 3x2 model, in which the sample is distributed in three study groups (over 53 years) and were evaluated at 10 weeks from baseline.

Detailed description

Objectives of the study: * Evaluate effectiveness of a physical exercise program for 10 weeks to improve fitness, cardiovascular, anthropometric and body composition parameters in people over 53 years. * Examine effects of exercise intervention delivered through a mobile application (WhatsApp) on fitness, cardiovascular risk factors, anthropometric and body composition in people over 53 years. Hypotheses of the study: * An intervention of exercise administered via mobile application (WhatsApp) is effective in reducing cardiovascular risk factors in people over 53 years. * An intervention of exercise administered via mobile application (WhatsApp) is effective to increase physical fitness in people over 53 years. * An intervention of exercise administered via mobile application (WhatsApp) is effective in reducing BMI, percent body fat; and in increasing the percentage of muscle mass in people over 53 years. * 10-weeks face-to-face intervention of physical exercise obtains greater improvements in fitness parameters than an intervention delivered via mobile application in people over 53 years. * 10-weeks face-to-face intervention of physical exercise obtains greater improvements in anthropometric and body composition than an intervention delivered via mobile application in people over 53 years.

Interventions

OTHERMobile group

The subjects in this group received the same intervention that trainning group but through a mobile application (whatsapp).

OTHERControl group

No received intervention.

OTHERTraining group

The main part of the session included a whole-body strength training, which incorporated chest press, shoulder press, lateral pull-down, seated row, shoulder flexion, chest pulley, hammer curl, biceps curl, triceps curl, triceps pushdown, leg extension, leg curl, lunge, squat, abdominal crunch. To control and equate the intensity between the TG and MG, a method based on the combined use of the prescribed number of repetitions and the OMNI Resistance Scale for the active muscles was used. Previous studies have described the method used for controlling exercise intensity (Colado et al., 2012; Colado et al., 2014). During 1-3 weeks subjects performed 25 min of exercise at 60% maximum heart rate (HRmax), during weeks 4-6 subjects performed 30 min of exercise at 70% HRmax and during weeks 7-10 subjects performed 35 min of exercise at 80% HRmax.

Sponsors

University of the Balearic Islands
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
53 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Have own mobile phone and Internet * Be clinically stable * Be able to perform physical activity * Be able to understand and complete the informed consent * Ability to cope assessment tests

Exclusion criteria

* Unable to perform physical activity * Have an acute or chronic disease * Have medical conditions or other physical problem that needs special attention (history of fracture of any upper or lower limb, dementia, psychological problems, neuromuscular disease, history of myocardial infarction, osteoporosis, cancer, diabetes).

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Muscle massChange from Baseline in Muscle mass at 10 weeksMuscle mass was measured using Bioimpedance scale (Tanita Body Fat Monitor Scale plus, Model BF-556) is used
Change from Baseline in Maximum hand grip strength (dynamometry)Change from Baseline in Maximum hand grip strength (dynamometry) at 10 weeksThe manual pressure force was measured with a digital force gauge (TKK 5001 Grip-A; Takey, Tokyo, Japan) and the results are recorded in kilograms
Change from Baseline in Aerobic capacityChange from Baseline in Aerobic capacity at 10 weeksAerobic capacity was measured using 2-Minute Step Test.
Change from Baseline in Static BalanceChange from Baseline in Static Balance at 10 weeksStatic balance measurement was conducted using the Flamingo test (Committee of Experts on Sport Research, 1988).
Change from Baseline in Waist circumferenceChange from Baseline in Waist circumference at 10 weeks
Change from Baseline in Body fatChange from Baseline in Body fat at 10 weeksBody fat was measured using Bioimpedance scale (Tanita Body Fat Monitor Scale plus, Model BF-556) is used

Secondary

MeasureTime frameDescription
Change from Baseline in HeightChange from Baseline in Height at 10 weeksThe height was measured as close to the millimeter using the mobile rod (Seca 217).
Change from Baseline in WeightChange from Baseline in Weight at 10 weeksThe weight was measured using bioelectrical impedance scales (Tanita Body Fat Monitor Scale plus, Model BF-556).
Change from Baseline in Systolic Blood PressureChange from Baseline in Systolic Blood Pressure at 10 weeksThe Systolic Blood Pressure was measured using Omron Elite 7300W (Omron Healthcare Inc, Bannockburn, IL, USA)
Change from Baseline in Dyastolic Blood PressureChange from Baseline in Dyastolic Blood Pressure at 10 weeksThe Dyastolic Blood Pressure was measured using Omron Elite 7300W (Omron Healthcare Inc, Bannockburn, IL, USA)
Change from Baseline in Physical activity levelsChange from Baseline in Physical activity levels at 10 weeksTo measure levels of physical activity of the participants used the International Physical Activity Questionnaire (IPAQ) (Craig et al., 2003)

Countries

Spain

Outcome results

None listed

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