Status:

COMPLETED

Impact of Fish Oil Dose on Tissue Content and Function

Lead Sponsor:

University of Stirling

Collaborating Sponsors:

Danone Nutricia Research

Conditions:

Aging

Sarcopenia

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

In this 5-month study, we will track the incorporation and washout of n-3 PUFA into different tissues following two different dosing strategies in healthy young and older volunteers. All groups will b...

Detailed Description

Skeletal muscle is crucial for health and accounts for approximately 40% of total body mass. A loss of skeletal muscle mass is seen in the process of ageing, with reductions between 0.2%-0.5% of muscl...

Eligibility Criteria

Inclusion

  • Provide valid informed consent prior to any study procedure
  • Males and females 18-35 years of age or 60+ years of age
  • BMI between 18-29 kg/m2
  • Free of musculoskeletal injuries
  • Willing to avoid alcohol in the 48-h period prior to the visits
  • Willing to sustain their current diet and lifestyle and not to make conscious changes for the duration of the study
  • An omega-3 status of less than 20% seen in whole blood taken during the screening visit.
  • Willing to sustain current use of supplementation/anti-depressants or other medication not interfering with the study results.
  • Women: not currently pregnant, not intending to become pregnant in the coming 5 months or lactating.
  • Women: willing to maintain current use of contraceptives or post-menopausal supplementation if any for the duration of the study.
  • Not allergic to fish, shellfish, seaweed, iodine, anesthetics, nickel or chrome.

Exclusion

  • Smoker
  • Adherence to a strict vegan/vegetarian diet
  • Treatment for cardiovascular diseases or blood pressure \>140/90 mmHg
  • Any diseases or medication that cause fat malabsorption (intestine issues such as celiac disease, Crohn's disease,chronic pancreatitis, or cystic fibrosis; liver and biliary disease, diarrhoea, steatorrhea)
  • Diabetes or other (metabolic) disease that induce muscle wasting
  • Surgery in prior 6 months
  • Currently being on FO supplementation
  • Current participation in another clinical trial, or in a trial within the past month
  • For women: pregnant, intention to get pregnant during the course of the study or lactating

Key Trial Info

Start Date :

November 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 15 2023

Estimated Enrollment :

28 Patients enrolled

Trial Details

Trial ID

NCT04772040

Start Date

November 1 2021

End Date

June 15 2023

Last Update

December 4 2023

Active Locations (1)

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University of Stirling

Stirling, Stirlingshire, United Kingdom, FK9 4LA