- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06259825
Omega-3-Index Response to Eating Poultry Foods Naturally Enriched With Omega-3 Polyunsaturated Fatty Acids
Omega-3-Index Response to Eating Poultry Foods Naturally Enriched With Omega-3 Polyunsaturated Fatty Acids: A Randomized Controlled Trial in Healthy Saudi Adults
Diets low in seafood omega-3 polyunsaturated fatty acids (PUFAs) are very prevalent. Such diets have recently been ranked as the sixth most important dietary risk factor-1.5 million deaths and 33 million disability-adjusted life-years worldwide are attributable to this deficiency. Wild oily fish stocks are insufficient to feed the world's population, and levels of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in farmed fish have more than halved in the last 20 years.
The primary objective of this randomised, double-blinded, controlled nutritional trial will be to test if consumption of at least 4 servings of omega-3 PUFA-enriched chicken-meat and 4 enriched eggs per week, over a 4-month period, results in measurably higher blood levels of EPA and DHA in healthy Saudi adults.
This will be a randomised double-blind interventional study. Eighty adult male and female participants (age ≥ 18 years of age) will be asked to eat at least 4 portions of omega-3-PUFA enriched (or control) chicken-meat per week, and at least 4 omega-3-PUFA enriched (or control) eggs per week, for 4 months. Participants will be assessed at baseline and at monthly intervals for 4 months. Assessments at these visits will include; comprehensive lifestyle and medical history; food frequency questionnaire; 3 days food record; height, weight, waist and hip circumferences; blood sampling; participant well-being and adverse events. Measurement of plasma and red blood cell levels of EPA, DHA and Docosapentaenoic acid (DPA) will be performed at baseline and at study end using gas chromatography-mass spectroscopy.
The primary end point will be the change in red blood cell omega-3-index (sum of EPA and DHA expressed as percentage of total fatty acids in erythrocyte membranes) at 4 months. The nutritional trial will be analyzed on an intension to treat basis. Repeated measures ANOVA will be used to compare the two study groups. The study will be reported in accordance with the CONSORT (Consolidated Standards of Reporting Trials) 2010 statement.
Study Overview
Status
Conditions
Detailed Description
STUDY RATIONALE
In this randomized, double-blinded, controlled trial, the investigators aim to quantify the impact of regular consumption of omega-3 PUFA enriched chicken-meat and eggs over a four month period, in a healthy Saudi population.
STUDY AIMS AND OBJECTIVES.
The primary objective of this study will be to assess the red blood cell omega-3 index response of healthy Saudi adults to regular consumption of omega-3 PUFA-enriched chicken-meat and eggs. The red blood cell omega-3 index is calculated as the sum of EPA and DHA expressed as a percentage of total fatty acids in erythrocyte (red cell) membranes.
Secondary objectives include;
- The assessment of red cell and plasma EPA, DPA and DHA responses to regular consumption of omega-3 PUFA-enriched chicken-meat and eggs.
- The comparison of baseline red cell and plasma levels of EPA, DPA and DHA, amongst Saudi residents who regularly consume oily fish with those that do not regularly consume oily fish, and
- The assessment of whether the red cell and plasma omega-3 index responses to the omega-3-PUFA enriched foods differs between those that do, and those who do not, include oily fish in their weekly diet.
TRIAL DESIGN.
This will be a randomised double-blind interventional study. The trial will be performed in accordance with the Declaration of Helsinki.
STUDY PARTICIPANTS
80 healthy, community dwelling, participants will be recruited to the study.
RANDOMIZATION AND MASKING
Participants will be randomized to either of two arms;
- Control / Placebo Intervention: Consumption of at least 4 portions of standard chicken-meat and at least 4 standard eggs per week, for 4 months.
- Experimental Intervention: Consumption of at least 4 portions of omega-3-PUFA enriched chicken-meat and at least 4 omega-3-PUFA enriched eggs per week, for 4 months.
STUDY CONDUCT
Participants will attend the study center at the screening and baseline visits and at study end (month 4). They will be contacted by telephone at monthly intervals (Months 1, 2 and 3).
At the screening visit, a comprehensive lifestyle and medical history will be taken, a food frequency questionnaire will be completed to capture food intake over the previous year; a 3 days food record will be arranged to capture the current dietary intake of participants; and satisfaction of the inclusion and exclusion criteria will be evaluated.
At the baseline visit, if all inclusion and exclusion criteria are satisfied, participants will be randomized to either the control or the interventional arm of the study.
At both the baseline and month 4 visits, height, weight, waist and hip circumference will be measured, allowing calculation of both the body mass index and the waist-hip ratio. At these two clinic visits fasting blood samples will be taken to allow measurement of plasma and red cell levels of EPA, DPA and DHA, and also to allow storage of plasma aliquots for future research measurements. Participants will be asked to fast, not drink tea or coffee, not smoke and not engage in intense exercise from midnight (minimum 8 hours), prior to the baseline and end-of-study visits. Participants may drink water and take essential medications on these mornings.
At the month 1, 2 and 3 telephone calls, and at the month 4 visit, frequency of consumption of chicken-meat, eggs and fish, during previous week, will be assessed, as will concurrent medications and participant wellbeing.
Participants will be asked to avoid taking long-chain omega-3 PUFA supplements, for the duration of the study.
NUTRITIONAL INTERVENTION
The poultry meat and eggs will be enriched by feeding chickens a complete feed which includes algae, which is a rich source of omega-3 PUFAs (OmegaPro, Humanitiv, Meath, Ireland). Omega-3 PUFA enriched chicken (whole chickens, breasts, thighs and drums) and eggs, or the appropriate control chicken and control eggs, will be delivered to the homes of study participants at regular intervals (weekly or two-weekly), so that both they, and up to three additional family members, will be able to eat at least 4 servings per week of chicken meat, and at least 4 eggs weekly over the 4 month study period. The chicken-meat will be delivered frozen, and the eggs will be delivered refrigerated.
MEASUREMENT OF RED CELL AND PLASMA LEVELS OF FATTY ACIDS
Measurement of plasma and red cell levels of EPA, DPA and DHA will be performed at a laboratory with specific expertise in lipid analyses. Total lipids will be extracted from plasma and red cells using a modified Folch method. Phospholipids will be separated from neutral lipids by 1-dimensional thin-layer chromatography. Fatty acid methyl esters will be prepared by direct transesterification and separated using gas chromatography-mass spectrometry allowing quantification of 28 distinct fatty acid peaks. Plasma levels of omega-3-PUFAs will be expressed in microgram/gram, and red cell levels as a percentage of total fatty acids in erythrocyte membranes. The erythrocyte or red cell omega-3 index is calculated as the sum of EPA and DHA expressed as percentage of total fatty acids in erythrocyte membranes.
STATISTICAL ANALYSIS
Analyses and Reporting The study will be analyzed on an intension to treat basis. Standard summary statistics (mean, standard deviation, median, range, %) will be used to describe baseline characteristics of the participants.
Repeated measures ANOVA will be used to compare the 2 study groups. The study will be reported in accordance with the CONSORT (Consolidated Standards of Reporting Trials) 2010 statement.
Sample Size Considerations The primary end point will be the change in red cell omega-3-index at 4 months. In previous studies, the standard deviation of repeated measures of the erythrocyte omega-3 index has been found to be 0.5%. Hence with 80 participants, the study will have in excess of 95% power to detect a difference of 1% in the change from baseline in the omega-3 index between those eating enriched foods versus those eating control foods, at a 2-sided alpha-level of 0.05.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Alice V Stanton, MB, PhD
- Phone Number: +353872885480
- Email: astanton@rcsi.ie
Study Contact Backup
- Name: Salwa Albar, BSc, PhD
- Phone Number: +966505317160
- Email: salbar1@kau.edu.sa
Study Locations
-
-
-
Jeddah, Saudi Arabia, 21589
- Recruiting
- Department of Food Science and Nutrition, King Abdulaziz University
-
Contact:
- Salwa A Albar, BSc, PhD
- Phone Number: +966505317160
- Email: salbar1@kau.edu.sa
-
Contact:
- Hala F AL-Marzouki, BSc, MSc
- Phone Number: +966504663559
- Email: hfalmarzoukii@kau.edu.sa
-
Principal Investigator:
- Salwa A Albar, BSc, PhD
-
Sub-Investigator:
- Hala F AL-Marzouki, BSc, MSc
-
Sub-Investigator:
- Hadeil M Alsufiani, BSc, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adults (≥ 18 years and < 70 years)
- Regular consumers (≥ 4 portions weekly) or willing to be regular consumers of chicken-meat.
- Regular consumers (≥ 4 eggs weekly) or willing to be regular consumers of eggs.
- Able to give informed consent.
Exclusion Criteria:
- Concurrent or recent (within last 3 months) regular intake of long-chain omega-3-PUFA supplements (containing EPA, DPA and/or DHA).
Previous diagnosis of;
- significant cardiovascular disease (e.g. myocardial infarction, coronary intervention, or stroke),
- significant mental ill-health (e.g. major depression, psychosis or dementia) or
- a haemoglobinopathy such as sickle cell anaemia or thalassemia .
- Any other serious medical condition that may adversely affect the patient's safety, limit the subject's ability to participate in the study, comply with follow-up requirements or impact the scientific integrity of the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: Control Chicken-meat and Control Eggs
Consumption of at least 4 portions of standard chicken-meat and at least 4 standard eggs per week, for 4 months.
|
At least four portions of standard chicken-meat (whole chickens, breasts, thighs and drums) and at least four standard eggs will be consumed weekly for 4 months.
|
Experimental: Omega-3 Chicken-meat and Omega-3 Eggs
Consumption of at least 4 portions of omega-3-PUFA enriched chicken-meat and at least 4 omega-3-PUFA enriched eggs per week, for 4 months.
|
Other: Omega-3 polyunsaturated fatty acid, naturally enriched, poultry foods (chicken-meat and eggs)
At least four portions of omega-3 PUFA enriched chicken-meat (whole chickens, breasts, thighs and drums) and at least four omega-3 PUFA enriched eggs will be consumed weekly for 4 months.
The poultry meat and eggs will be enriched by feeding chickens a complete feed which includes algae, which is a rich source of omega-3 PUFAs (OmegaPro, Humanitiv, Meath, Ireland).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline in the red cell omega-3 index at 4 months
Time Frame: 4 months (16 weeks)
|
The difference between the red cell omega-3 index at baseline and at 4 months.
The red blood cell omega-3 index is calculated as the sum of EPA and DHA expressed as a percentage of total fatty acids in erythrocyte (red cell) membranes.
|
4 months (16 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in red cell EPA
Time Frame: 4 months (16 weeks)
|
The difference between red cell levels of eicosapentaenoic acid (EPA) at baseline and at 4 months
|
4 months (16 weeks)
|
Change in red cell DPA
Time Frame: 4 months (16 weeks)
|
The difference between red cell levels of docosapentaenoic acid (DPA) at baseline and at 4 months
|
4 months (16 weeks)
|
Change in red cell DHA
Time Frame: 4 months (16 weeks)
|
The difference between red cell levels of docosahexaenoic acid (DHA) at baseline and at 4 months
|
4 months (16 weeks)
|
Change in plasma EPA
Time Frame: 4 months (16 weeks)
|
The difference between plasma levels of eicosapentaenoic acid (EPA) at baseline and at 4 months
|
4 months (16 weeks)
|
Change in plasma DPA
Time Frame: 4 months (16 weeks)
|
The difference between plasma levels of docosapentaenoic acid (DPA) at baseline and at 4 months
|
4 months (16 weeks)
|
Change in plasma DHA
Time Frame: 4 months (16 weeks)
|
The difference between plasma levels of docosahexaenoic acid (DHA) at baseline and at 4 months
|
4 months (16 weeks)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
A comparison of baseline plasma and red cell levels of EPA, DPA and DHA, amongst Saudi residents who regularly consume oily fish with those that do not regularly consume oily fish.
Time Frame: Baseline
|
A comparison of baseline plasma and red cell levels of EPA, DPA and DHA, amongst Saudi residents who regularly consume oily fish with those that do not regularly consume oily fish.
|
Baseline
|
An assessment of whether the plasma and red cell omega-3 index responses to the omega-3-PUFA enriched foods differs between those that do, and those who do not, include oily fish in their weekly diet.
Time Frame: 4 months (16 weeks)
|
An assessment of whether the plasma and red cell omega-3 index responses to the omega-3-PUFA enriched foods differs between those that do, and those who do not, include oily fish in their weekly diet.
|
4 months (16 weeks)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Salwa Albar, BSc, PhD, King Abdulaziz University
- Principal Investigator: Alice V Stanton, MB, PhD, Royal College of Surgeons in Ireland
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- KAU-664-23
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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