Actively Recruiting
Effectiveness of Gut Microbiota-targeted Diatery Intervention Among Older People Living With HIV
Led by Fudan University · Updated on 2024-09-26
110
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to conduct a dietary intervention targeting HIV specific gut microbiota alterations for primary atherosclerotic cardiovascular disease (ASCVD) prevention and evaluate its effectiveness in preventing ASCVD among older people living with HIV (PLWH).
CONDITIONS
Official Title
Effectiveness of Gut Microbiota-targeted Diatery Intervention Among Older People Living With HIV
Who Can Participate
Eligibility Criteria
You may qualify if you...
- HIV-infected patients diagnosed according to China AIDS diagnosis and treatment guidelines
- Aged 40 years and above
- At risk of cardiovascular disease with any two risk factors: dyslipidemia, diabetes or elevated blood glucose, smoking, hypertension or elevated blood pressure, metabolic syndrome, overweight/obesity; or Pooled Cohort Equations score over 5%
- Predicted survival time greater than 1 year
- No plans to leave the study area in the next 3 months
- Voluntary participation and signing informed consent
You will not qualify if you...
- Previous history of cardiovascular disease
- HIV-related neurocognitive impairment, Alzheimer's disease, dementia, or serious opportunistic infections
- Currently suffering from malignant tumors or gastrointestinal diseases; aversion to eating
- Allergy to nuts or fish
- Taking medicinal calcium over 1000 mg per day or omega-3 supplements
- Planning to become pregnant within 6 months
- Participation in other HIV-related or dietary intervention scientific studies
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Third People's Hospital of Shenzhen
Shenzhen, China
Actively Recruiting
Research Team
J
Junwen Yu, Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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