- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06654362
The Effect of Multimodal Nutrition Intervention on Glucose and Lipid Parameters of Arfa Iron and Steel Company Workers
The goal of this clinical trial is to investigate the impact of nutritional interventions on glycemic and lipid profile factors among workers.
The main questions it aims to answer are:
Does nutritional interventions (include: nutritional education and Change in the Factory Restaurant's Menu improve glycemic and lipid profile factors among workers? Researchers will compare glycemic and lipid profile factors among workers before and after nutritional intervention .
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Yazd, Iran, Islamic Republic of
- Shahid Sadoughi University of Medical Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- be Arfa's company worker
Exclusion Criteria:
- individuals who were diagnosed with any type of cancer
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Arfa's company workers
all interventions administer to this arm
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Total Cholesterol, mg/dL
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
|
Total triglycerides, mg/dL
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
|
Low-density lipoprotein, mg/dL
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
|
High-density lipoprotein, mg/dl
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
|
Fast blood sugar, mg/dL
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
|
serum glutamic oxaloacetic transaminase, IU/L
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
|
serum glutamic pyruvic transaminase, IU/L
Time Frame: From enrollment to the end of intervention at 6 months
|
From enrollment to the end of intervention at 6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRSSU.SPHREC.1402.042
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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