A Comparison of the Effects of Krill Oil and Fish Oil Supplementation on Muscle Function in Older Adults

March 25, 2025 updated by: Stuart Gray, University of Glasgow

A Comparison of the Effects of Krill Oil and Fish Oil Supplementation on Muscle Function in Older Adults: a Randomised Controlled Pilot Study

The aim of the study is to compare the effects of Krill Oil and Fish Oil supplementation on muscle function in older adults. The secondary aim is to investigate the mechanisms underlying the beneficial effects previously observed.

Study Overview

Study Type

Interventional

Enrollment (Actual)

61

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Scotland
      • Glasgow, Scotland, United Kingdom
        • Stuart Robert Gray

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Older adults (aged 60 years or older). BMI less than 30kg/m2

Exclusion Criteria:

  • Participants (diagnosed and being treated for a pre-existing medical condition (cancer, kidney disease, liver disease, diabetes mellitus and cardiovascular disease, uncontrolled hypertension, gait disturbances limiting the ability to perform assessments of muscle function, dementia, affecting muscles known to use drugs (e.g., steroids). History of allergy to fish or fish oil and regular consumption of more than1portion of oily fish per week or use of fish oil or krill oil supplements will also be excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Active Comparator: Fish oil
Fish oil 4 g/day
EPA rich fish oil
Active Comparator: Krill oil
Krill oil 4g/day
Superba Krill Oil
Placebo Comparator: Placebo
Vegetable oil 4g/day
Mixed vegetable oil

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in knee extensor maximal isometric torque ( MVC)
Time Frame: Change from baseline to 16 weeks
Knee extensor maximal isometric torque measured during a maximal voluntary contraction
Change from baseline to 16 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in fat mass
Time Frame: Change from baseline to 16 weeks
Whole body fat mass measured by measured via bio-electrical impedance
Change from baseline to 16 weeks
Change in lean mass
Time Frame: Change from baseline to 16 weeks
Whole body lean mass measured by measured via bio-electrical impedance
Change from baseline to 16 weeks
Blood sample
Time Frame: Change from baseline to 16 weeks
Red Blood Cell Omega-3 levels
Change from baseline to 16 weeks
Change in Grip strength
Time Frame: Change from baseline to 16 weeks
Grip strength measured with a hand held dynamometer
Change from baseline to 16 weeks
Change in Muscle thickness
Time Frame: Change from baseline to 16 weeks
Vastus lateralis muscle thickness measured by ultrasound
Change from baseline to 16 weeks
Force steadiness during submaximal isometric knee extensor contractions
Time Frame: Change from baseline to 16 weeks
Measured by using intramuscular iEMG
Change from baseline to 16 weeks
Neuromuscular Junction (NMJ)
Time Frame: Change from baseline to 16 weeks
Measured by iEMG
Change from baseline to 16 weeks
Change in gait speed
Time Frame: Change from baseline to 16 weeks
Time taken to walk 4 metres at a normal walking pace
Change from baseline to 16 weeks
Change in Chair rise time
Time Frame: Change from baseline to 16 weeks
A 30-second sit-to-stand test measured functional abilities
Change from baseline to 16 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Step Time (Sec)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Cycle Time (Sec)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Step Length (CM)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Stride Length (CM)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
H-H Base Support (CM)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Single Support (%GC)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Double Support (%GC)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Swing (%GC)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Stance (%GC)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Step/ Extremity Ratio
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Toe In/ Out (deg)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Distance (CM)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Ambulation Time (Sec)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Velocity (CM/Sec)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Mean Normalized Velocity
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Number of Steps
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Cadence (Steps/Min)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Step Time Differential (Sec)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Step Length Differential (CM)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks
Cycle Time Differential (Sec)
Time Frame: Change from baseline to 16 weeks
Measured during a 4m walk using a gaitrite mat
Change from baseline to 16 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2023

Primary Completion (Actual)

February 1, 2024

Study Completion (Actual)

April 1, 2024

Study Registration Dates

First Submitted

May 11, 2023

First Submitted That Met QC Criteria

May 11, 2023

First Posted (Actual)

May 22, 2023

Study Record Updates

Last Update Posted (Actual)

March 30, 2025

Last Update Submitted That Met QC Criteria

March 25, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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