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Effects of Multidomain Training of Health With Aging (Train-Old)

Psycho-physiological Effects of Multidomain Training in Adults and Older Adults

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05481346
Acronym
Train-Old
Enrollment
80
Registered
2022-08-01
Start date
2022-07-28
Completion date
2022-12-30
Last updated
2022-08-02

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

Conditions

Cardiovascular Diseases, Frailty, Memory Loss, Muscular Atrophy, Sarcopenia

Keywords

older adults, Healthy aging, Resistance training, cognitive training, cardiovascular training

Brief summary

The current study aims to determine the effect of a multidomain intervention (physical fitness, motivational and cognitive training) on body composition, sarcopenia, cardiovascular health, physical fitness, functional capacity, quality of life, frailty, emotional state and cognitive status in elderly participants, through a randomized controlled trial, to determine its suitability and recommend it as a preventive and health strategy for community-dwelling older adults.

Interventions

PROCEDUREMultidomain training

The training program has a duration of 18 weeks with 2 training sessions per week. The training will have a gradual progression of intensity. One day they train two blocks of strength and one block of cognitive exercises and on the second day, they train one block of power, one block of strength+cognitive and one block of aerobic training. All sessions are 60 minutes long (10 minutes of warm-up, 40 minutes of training and 10 minutes of cool-down). Classes are in small groups of no more than 8 members.

Sponsors

Universidad de Almeria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be randomly assigned to an experimental group that will perform the physical exercise program and a control group that will perform nothing and continue with their normal lifestyle routines, without any physical activity.

Eligibility

Sex/Gender
ALL
Age
55 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

1. Subject has provided written and dated informed consent to participate in the study. 2. Subject is a male or female between 55 and 90 years of age, inclusive. 3. Subject is in good health as determined by a health history questionnaire and has been provided clearance from their personal physician. 4. Subject is untrained in resistance and aerobic exercise (does not participate in structured physical activity, including walking, more than 3 times per week). 5. Ability to walk independently without any gait aid

Exclusion criteria

1. Perform high-intensity aerobic exercise on a consistent basis (\>180 min-week). 2. Be performing some other regular and systematic strength training program during the intervention in the first half of 2022. 3. Have a body mass index greater than 35. 4. Have a diagnosis of ischemic heart disease. 5. Have a diagnosis of severe aortic stenosis, uncontrolled arrhythmias, decompensated heart failure or acute myocarditis. 6. Possess uncontrolled blood pressure (TAS \>180 and TAD \>110). 7. Stroke. 8. Severe peripheral arterial disease. 9. Other illnesses such as recent thromboembolic disease, aortic aneurysm, clinically significant renal or hepatic insufficiency, severe COPD, clinically significant acute infections, severe psychiatric illness, uncontrolled metabolic disease, limiting locomotor pathology or musculoskeletal disease worsened by exercise, hormone therapy at the time or one year prior, being a woman with surgical menopause. 10. Other pathologies that contraindicate the practice of physical exercise, collected in the previous medical examination that all participants must undergo.

Design outcomes

Primary

MeasureTime frameDescription
Body Weight in KilogramsChange from Baseline body weight (kg) at 18 weekswas measured after removal of shoes and heavy outer clothing, using a Tanita BC-418 MA or InBody equipment to the nearest 0.1 kg.
Height in MetersChange from Baseline standing height (cm) at 18 weeksStanding height without shoes was measured using a Seca 202 stadiometer (Seca, Hamburg, Germany) to the nearest 0.1 cm.
Body Mass Index (BMI)Change from Baseline Body Mass Index (BMI): (kg/m^2) at 18 weekswas calculated as the ratio of weight to squared height in kg/m\^2
% Fat MassChange from Baseline bioelectrical impedance % fat mass at 18 weeks% fat mass was measured after removal of shoes and heavy outer clothing, using a Tanita BC-418 MA or InBody equipment to the nearest 0.1 kg.
Muscle quality sarcopeniaChange from Baseline to 18 weeksSarcopenia will be assessed taking into account the reference values established for muscle quality. The muscle quality will be measure by hand grip strength test. This test will be performance with manual dynamometry (TKK 5401; Scientific Instruments Co., Ltd., Tokyo, Japan). Maximal isometric upper limb strength will be performance by maximal isometric strength. Upper strength will be register by kilogrammes. Higher value show high strength.

Secondary

MeasureTime frameDescription
Change heart rateChange from Baseline to 18 weeksHeart rate will be assessed by means of an automatic device (Colin BP 880, Inc., Tampa, FL). This is noninvasive technique. The result will be register in number of pulse per minutes (heart rate).
Gait speedChange from Baseline to 18 weeksGait speed will be measure by 4. 6 and 10 meter test. This is easy physical test in with the participant have to walk 4. 6 and 10 metres as faster as possible. The result will be register in seconds. Less time indicates better functional ability.
Time up and go test changeChange from Baseline to 18 weeksTime up and go test measure the functional capacity of getting up, walking and sitting down form a chair. Participant have to performance this test as faster as possible. This is a easy physical test. Total seconds are records. Less seconds indicates better functional ability.
Short physical performance battery (SPPB)Change from Baseline to 18 weeksShort physical performance battery (SPBB) include three test (balance, chair stand test and gait speed) and report a final score. Chair stand test and gait speed were describe in other outcome. Balance test is a easy physical test. The participant must maintain three balancing positions for 10 seconds to overcome it. Each test offers a different score. Higher score show better functional capacity.
FragilityChange from Baseline to 18 weeksFrailty will be defined in relation to Fried's frailty phenotype (Fried et al., 2001), based on 5 criteria: unintentional weight loss, exhaustion, weakness, slow walking speed and low physical activity.
Change Blood pressureChange from Baseline to 18 weeksBlood pressure and heart rate will be assessed by means of an automatic device (Colin BP 880, Inc., Tampa, FL). This is noninvasive technique. The result will be register in millimeters of mercury (bood pressure) and number of pulse per minutes (heart rate).
DepressionChange from Baseline to 18 weeksDepression will be measured through the Center for Epidemiological Studies Depression Scale-Revised (CESD-R) (Van Dam & Earleywine, 2011), is a 20-item questionnaire that can be used to measure levels of depressive symptoms among elderly participants. The CESD-R consists of 16 items of negative affect and 4 items of positive affect.
Cognitive flexibilityChange from Baseline to 18 weeksthe Stroop test measures the ability to classify information selectively. It consists of 3 phases and requires discerning between colors and words without making mistakes.
Attention testChange from Baseline to 18 weeksthe Trail Making test will also assess flexibility of thought and visuospatial ability. It consists of joining numbers and words in a numerical sequence without error.
PSQ testChange from Baseline to 18 weeksTo evaluate the factors that influence the general state of health, specifically stress. It evaluates six factors: Tension-Instability-Fatigue; Social Acceptance of Conflict; Energy and Fun; Overload; Satisfaction for self-fulfillment; Fear and anxiety.
TMMS-24Change from Baseline to 18 weeksTrait-Meta Mood Scale (TMMS) emotional states
Satisfaction with lifeChange from Baseline to 18 weeksThe Satisfaction with Life Scale is a 4-item instrument with a Likert-type scale ranging from 1 to 7 points measuring overall subjective happiness by means of statements in which participants rate themselves or compare themselves with others. Two items ask people to describe themselves using absolute rating criteria of their lives or rating criteria with respect to others, while the other two items present brief descriptions of happy or unhappy people and respondents are asked to indicate the degree to which they identify with that description.
Change Chair stand testChange from Baseline to 18 weeksChair stand test measure the functional capacity. This is a easy physical test. This test measures the functionality of getting up and sitting down from a chair five times. The participant have to performance the test as faster as possible. The total time is recorded in seconds. A better time indicates better functional ability.
Change Upper and Lower strengthChange from Baseline to 18 weeksMaximal isometric upper limb strength will be performance by maximal isometric strength of knee extension and biceps flexion with load cell. Maximal isometric lower limb will be registered in newton. Higher value show high strength.
Health-related qualityChange from Baseline to 18 weeksSF-36 quality of life questionnaire
Cardiorrespiratory 6 minutes walk testChange from Baseline to 18 weekscardiorespiratory endurance test that evaluates the distance covered in 6 minutes.

Countries

Spain

Contacts

Primary ContactPablo Jorge Marcos Pardo, PhD
pjmarcos@ual.es+34 950214791
Backup ContactPablo Jorge Marcos Pardo, PhD
pablomarcospardo@gmail.com+34 950214791

Outcome results

None listed

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