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A multi-omics-driven study on the prediction of exercise responses in overweight/obese patients with knee osteoarthritis

A Multi-omics-Driven Study on Predicting Exercise Responses in Patients with Overweight/Obese Knee Osteoarthritis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124629
Enrollment
Unknown
Registered
2026-05-14
Start date
2026-05-20
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Knee osteoarthritis

Interventions

intervention group:The intervention group will strictly follow the 27-week standardized exercise intervention protocol validated in the research team’s previous studies. This protocol combines "3 week
Retrospective cohort:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: Study Population for the Retrospective Cohort Study Inclusion Criteria: 1. Age >= 45 years; 2. BMI >= 24.0 kg/m²; 3. Meets diagnostic criteria for knee osteoarthritis and exhibits symptoms (NRS >= 3); 4. Has completed a 6-month standardized strength training intervention and has complete baseline and post-intervention follow-up data (clinical phenotype and blood samples). Study Participants for the Prospective Cohort Inclusion Criteria: 1. Age >= 45 years; 2. BMI >= 24.0 kg/m²; 3. Meets diagnostic criteria for knee osteoarthritis and exhibits symptoms (NRS >= 3); 4. Is alert and able to cooperate with study interventions and data collection; 5. Provides informed consent and signs the informed consent form.

Exclusion criteria

Exclusion criteria: Study Population for the Retrospective Cohort Exclusion criteria: 1. Age > 75 years; 2. History of total knee arthroplasty; 3. Concurrent severe systemic diseases (e.g., cancer, severe cardiovascular or cerebrovascular disease) or cognitive impairment that precludes participation in the intervention and assessment. Study Population for the Prospective Cohort Exclusion criteria: Same as those for the retrospective cohort.

Design outcomes

Primary

MeasureTime frame
knee pain;

Secondary

MeasureTime frame
Lower limb muscle strength;balance function;Walking ability;Ability to go up and down stairs;Abdominal muscle endurance;center for epidemiological studies depression scale;Life quility;Bio-omics biomarkers;Knee stiffness;Difficulity in daily activities;

Countries

China

Contacts

Public ContactHongbo Chen

Peking University Third Hospital - Nursing Department

dabo1988@126.com+86 155 0111 6799

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026