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The Efficacy of Exercise Prescription Based on Multimodal Smart Health Examination Data Combined with Artificial Intelligence Technology on Physical Fitness and Exercise Habits in Sedentary and Chronically Fatigued Young Adults

The Efficacy of Exercise Prescription Based on Multimodal Smart Health Examination Data Combined with Artificial Intelligence Technology on Physical Fitness and Exercise Habits in Sedentary and Chronically Fatigued Young Adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107730
Enrollment
Unknown
Registered
2025-08-18
Start date
2025-03-13
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

fatigue

Interventions

AI Exercise Prescription Group:A total of 100 participants received personalized AI-generated exercise prescriptions based on multimodal health data and adaptive AI algorithms. Prescription parameters
General Exercise Group:A total of 100 participants in the conventional exercise group received standardized exercise guidelines. Both groups participated in structured classroom-based exercise interve
Teachers provided regular performance feedback to enhance engagement
All sessions were randomly audited by the research team to verify compliance with movement standards and intervention fidelity.

Sponsors

Guangzhou College of Commerce
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1 Aged 18–25 years; 2 Self-reported fatigue symptoms; 3 Fatigue Severity Scale (FSS) score >= 36 or VAS fatigue score >=1 (0–10 scale) (meeting either qualifies); 4 Sedentary lifestyle (<150 minutes of moderate-intensity exercise/week); 5 Able to complete the 3-month exercise intervention; 6 Capable of providing complete multimodal smart health exam data;

Exclusion criteria

Exclusion criteria: 1 Diagnosis of depression or anxiety disorders during the study period; 2 Use of psychoactive medications (e.g., opioids, antidepressants) that may affect mood; 3 Poor adherence to the exercise intervention; 4 Presence of contraindications to physical activity.

Design outcomes

Primary

MeasureTime frame
Fatigue Assessment;Lung Capacity;

Secondary

MeasureTime frame
1000m Run (Men) / 800m Run (Women) Time;50m Run Time;Sit-and-Reach Test;Standing Long Jump;1-Minute Pull-Ups (Male)/Sit-Ups (Female);VO2max Indirect Method;Heart Rate Recovery (HRR) ;6-Minute Walk Test (6MWT);Steps per day (steps/day) ;Moderate-intensity activity (heart rate) and duration;Sedentary time;BMI; International Physical Activity Questionnaire Short Form (IPAQ-SF);

Countries

china

Contacts

Public ContactDongruiqing

Guangzhou College of Commerce

294351531@qq.com+86 134 3782 5604

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026