- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05869526
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
Status
Completed
Conditions
Intervention / Treatment
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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FISHKRILL
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.