Actively Recruiting
Efficacy of a Health Empowerment Theory Based Health Information Literacy Promotion Intervention in Individuals With Metabolic Syndrome
Led by Meihua Ji · Updated on 2025-12-01
310
Participants Needed
4
Research Sites
69 weeks
Total Duration
On this page
Sponsors
M
Meihua Ji
Lead Sponsor
T
The Luhe Teaching Hospital of the Capital Medical University
Collaborating Sponsor
AI-Summary
What this Trial Is About
The ENRICH study is aimed to Enpower patieNts with metabolic syndrome (Mets) to increase their Risk perception and to acquire health Information necessary for Capability building and promotion of Health information literacy, as well as health outcomes. The purpose of this clinical trial is to evaluate the efficacy of this health information literacy promotion intervention based on Health Empowerment Theory in individuals with metabolic syndrome. The study aims to answer the following questions: Does the intervention improve health information literacy among study participants? Does the intervention lead to better health outcomes, including weight, waist circumference, BMI control, and metabolic health indicators (blood pressure, blood glucose, glycated hemoglobin, and blood lipids)? Participants will: Undergo the intervention program for 6 weeks (face to face and online) and will be assessed regularly to monitor changes in terms of their level of health information literacy and health outcomes.
CONDITIONS
Official Title
Efficacy of a Health Empowerment Theory Based Health Information Literacy Promotion Intervention in Individuals With Metabolic Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 75 years old
- Diagnosed with metabolic syndrome meeting at least 3 of the following: waist circumference ≥ 90 cm (men) / ≥ 85 cm (women), fasting glucose ≥ 6.1 mmol/L or OGTT 2h-glucose ≥ 7.8 mmol/L or diabetes treatment, blood pressure ≥ 130/85 mmHg or hypertension treatment, fasting triglycerides ≥ 1.70 mmol/L, fasting HDL-C < 1.04 mmol/L
- Aware of the condition and have basic reading and language communication skills
- Voluntarily agree to participate in the study
You will not qualify if you...
- Severe liver or kidney dysfunction, cancer, severe cardiovascular or cerebrovascular diseases, gout, or other conditions seriously endangering life requiring special diet
- Pregnancy
- History of mental illness or cognitive impairment
- Currently participating in other research projects
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Songzhuang Community Health Service Center
Beijing, Beijing Municipality, China, 101100
Actively Recruiting
2
Yuqiao Subdistrict Community Health Service Center
Beijing, Beijing Municipality, China, 101100
Completed
3
Li Yuan Community Health Service Center in Tongzhou District, Beijing
Beijing, Beijing Municipality, China, 101121
Enrolling by Invitation
4
Lucheng Subdistrict Community Health Service Center
Beijing, Beijing Municipality, China
Actively Recruiting
Research Team
M
Meihua Ji
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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