Health-Related Physical Fitness Level From Smartwatches

NCT ID: NCT06805422

Last Updated: 2025-08-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-01-01

Study Completion Date

2025-12-25

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Health-related physical fitness (HRPF) has demonstrated high clinical relevance, and its level is associated with the ability to perform activities of daily living with vigor and a lower risk of chronic disease. Consequently, exercise prescription guidelines recommend improving HRPF as a focus for prevention and rehabilitation programs. Measuring and tracking HRPF often requires specialized equipment and personnel, which are expensive and less applicable to the general population. Wearables may mitigate this issue by providing useful estimates of the HRPF.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Health-related physical fitness (HRPF) has high clinical relevance \[1\]. It is associated with the ability to perform activities of daily living with vigor and a lower risk of chronic disease \[2\]. Consequently, exercise prescription guidelines recommend improving HRPF as a focus for prevention and rehabilitation programs \[3\]. The American College of Sports Medicine (ACSM) \[3\] grouped the HRFP into five domains: cardiorespiratory endurance, body composition, muscular strength, muscular endurance, and flexibility. However, measuring and tracking the fitness levels for all HRPF domains requires specialized laboratory equipment and personnel, which are expensive and less applicable to the general population. Wearable technology mitigates this issue and has proven to be a reliable alternative capable of providing useful estimates of the HRPF \[4\] \[5\] \[6, 7\]. Previous work has predicted ACSM HRPF domains from anthropometric and laboratory bioelectrical impedance analysis data (BIA) \[8\] \[9\]. Nevertheless, their data are based on the National Fitness Award (NFA), a nationwide test used to assess the physical fitness of the general South Korean population that is collected using specialized laboratory equipment under the supervision of health professionals.

Current advances in wearables may allow us to estimate the fitness level for all HRPF domains using only smartwatch data, enabling economic, non-intrusive predictions and being available during the user's daily routine. The complete characterization of health-related fitness as a multidimensional depiction of the user's fitness status can be used to track health status continuously and to design specialized training prescriptions. The main goal of this study is to estimate the fitness level for all HRFP domains from data obtained from smartwatches during unsupervised activities of daily living. We hypothesized that data from smartwatches could be used to estimate the fitness levels from all HRPF domains.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Exercise Capacity Flexibility Strength and Endurance

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Aerobically trained

actively engaged in aerobic exercise training for at least 2 years

No interventions assigned to this group

Strength trained

actively engaged in weight training

No interventions assigned to this group

Not actively training

not engaged in regular aerobic or weight training exercise

No interventions assigned to this group

Highly flexible

determined by their flexibility scores

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Group 1 (Aerobically Trained)

* 20-60 years old
* actively training or competing over the past 2 years
* 3 or more days of vigorous activity accumulating approximately least 1500 MET min/week or 7 days of any combination of walking, moderate, or vigorous intense activities achieving a minimum of 3000 MET min/week

Group 2 (Strength trained)

* 20-60 years old
* actively training or competing over the past 2 years
* 3 or more days of muscle-strengthening exercise at an intensity of approximately 5 out of 10

Group 3 (Not actively training)

* 20-60 years old
* actively training or competing over the past 2 years
* 3 or more days of muscle-strengthening exercise at an intensity of approximately 5 out of 10

Group 5 (High flexibility)

* 20-60 years old
* Sit-and-reach performance is categorized as "very good" or excellent based on the American College of Sports Medicine's sit-and-reach evaluation criteria (Table 4.16 of ACSM's Guidelines for Exercise Testing and Prescription 9th edition).

Exclusion Criteria

* History of cardiovascular disease (Cardiac, peripheral vascular, or cerebrovascular disease)
* History of stable or unstable angina
* History of cardiac dysrhythmias causing symptoms or hemodynamic consequences
* History of hypertrophic cardiomyopathy
* History of cardiac valvular disease (e.g., aortic stenosis)
* History of pulmonary disease (Chronic obstructive pulmonary disease, asthma, interstitial lung disease, or cystic fibrosis)
* History of pulmonary embolus
* History of suspected or known aneurysm
* History of metabolic disease (Diabetes mellitus (type I or II), thyroid disorders, renal or liver disease
* History of renal disease
* History of neuromotor, musculoskeletal, or rheumatoid disorders that are exacerbated by exercise
* Current acute systemic infection, accompanied by fever and body aches.
* Pain or discomfort in the chest, neck, jaw, arms, or other areas that may be due to myocardial ischemia (lack of adequate circulation)
* Shortness of breath at rest, during daily activities, or with mild exertion
* Dizziness or syncope (fainting)
* Orthopnea (breathing discomfort when not in an upright position) or paroxysmal nocturnal dyspnea (interrupted breathing at night)
* Ankle edema (swelling)
* Palpitations (abnormal rapid beating of the heart) or tachycardia (rapid heartbeat)
* Intermittent claudication (cramping pain and weakness in legs, especially calves, during walking due to inadequate blood supply to muscles)
* Known heart murmur (atypical heart sound indicating a structural or functional abnormality)
* Unusual or unexplained fatigue
* Severe arterial hypertension (i.e., systolic blood pressure of \>200 mm Hg and/or a diastolic blood pressure of \>110 mm Hg) at rest.
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Kansas State University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Carl Ade, M.S., Ph.D.

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Kansas State Univeristy

Manhattan, Kansas, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

IRB-12223

Identifier Type: OTHER

Identifier Source: secondary_id

KansasSU

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Stress Resilience Study
NCT00891488 COMPLETED