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The effect of exercise intervention on random fatigue in the general population: a controlled study

The effect of exercise intervention on random fatigue in the general population: a controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000743
Enrollment
Unknown
Registered
2026-03-25
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Fatigue

Interventions

Experimental group:Once a week, 1.5 hours per session, over 24 weeks of structured exercise program.
Control Group:No other structured exercise interventions.

Sponsors

Shenzhen Baoan Authentic TCM Therapy Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18-80 years old (college students must be at least 18 years old, and the upper age limit for adult evening school students and community residents is 80 years old); 2. Students from Jiangyin, Jiangsu and Dezhou, Shandong, as well as permanent residents in Shenzhen communities; 3. No severe chronic diseases (such as severe cardiovascular diseases, impaired liver or kidney function, etc.); 4. Able to complete the questionnaire independently; 5. Voluntarily participate in this study and sign the informed consent form; 6. No contraindications to exercise and able to tolerate a 1.5-hour exercise class intensity each time.

Exclusion criteria

Exclusion criteria: 1. Suffer from mental disorders or cognitive impairments, unable to cooperate with the investigation and course participation; 2. Have contraindications for exercise (e.g., severe osteoporosis, joint deformities, acute injuries, etc.); 3. Have participated in similar exercise interventions or fatigue-related studies within the past 3 months; 4. Are unable to commit to participation for the next 24 weeks (e.g., due to long-term business trips, relocation, etc.); 5. Refuse to sign the informed consent form or withdraw from the study midway.

Design outcomes

Primary

MeasureTime frame
Fatigue Scale-14;

Secondary

MeasureTime frame
"Fatigue Severity Scale";

Countries

China

Contacts

Public ContactLi Jiaqi

Shenzhen Baoan Authentic TCM Therapy Hospital

drlijiaqi126@163.com18780146009

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026