Investigating the Effects of Krill Oil and Krill Protein on Post-exercise Muscle Protein Metabolism (KIPLING)

April 27, 2026 updated by: Stuart Gray, University of Glasgow

Investigating the Effects of Krill Oil and Krill Protein on Post-exercise Muscle Protein Metabolism: a Randomised Controlled Trial

The aim of the current study is to find out if krill oil can increase muscle building processes in response to resistance (weightlifting) type exercise. Others aim are to determine the effects of krill protein, and the interaction of krill oil and protein, on muscle building processes in response to resistance (weightlifting) type exercise.

Study Overview

Study Type

Interventional

Enrollment (Actual)

52

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

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

60 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Be 60 years old or older
  • Have a BMI of less than 35kg/m2
  • Be participating in structured exercise for less than 2h per week

Exclusion Criteria:

  • Diabetes
  • Severe cardiovascular disease
  • Seizure disorders,
  • Uncontrolled hypertension (>150/90mmHg at baseline measurement)
  • Cancer or cancer that has been in remission <5 years
  • Ambulatory impairments which would limit ability to perform assessments of muscle function
  • Dementia
  • Taking medication known to affect muscle (e.g., steroids)
  • Have an implanted electronic device (e.g., pacemaker/defibrillator/insulin pump),
  • Anticoagulant therapy
  • Allergies to seafood
  • Regular consumption of more than 1 portion of oily fish per week.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Vegetable oil + Carbohydrate
The vegetable oil will be a placebo control for the Krill oil (4g/day). The carbohydrate will be a placebo control for the Krill protein (20g)
This will be the control against the Krill oil
This will be the control for the Krill protein
Experimental: Vegetable oil + Krill protein
The vegetable oil will be a placebo control for the Krill oil (4g/day). Krill protein will be our active intervention (20g)
This will be the control against the Krill oil
Krill protein will be given to the participant following a resistance exercise bout.
Experimental: Krill oil + Carbohydrate
The Krill oil will be the active supplement for the intervention (4g/day). The carbohydrate will be a placebo control for the Krill protein (20g)
This will be the control for the Krill protein
Krill oil will be supplemented to see if they can gain strength and/or muscle mass following supplementation.
Experimental: Krill oil + Krill protein
Both the Krill oil (4g/day) and the Krill protein will be the active intervention supplements (20g)
Krill protein will be given to the participant following a resistance exercise bout.
Krill oil will be supplemented to see if they can gain strength and/or muscle mass following supplementation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post-exercise muscle protein synthesis
Time Frame: 3-7 hours
Muscle protein synthesis measured 3-7h after a single bout of resistance exercise
3-7 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Muscle thickness
Time Frame: Change from baseline to 8 weeks
Vastus lateralis muscle thickness measured by ultrasound
Change from baseline to 8 weeks
Change in grip strength
Time Frame: Change from baseline to 8 weeks
Grip strength measured with a Jamar dynamometer
Change from baseline to 8 weeks
Change in fat mass
Time Frame: Change from baseline to 8 weeks
Whole body fat mass measured by BIA
Change from baseline to 8 weeks
Change in lean mass
Time Frame: Change from baseline to 8 weeks
Whole body lean mass measured by BIA
Change from baseline to 8 weeks
Change in muscle strength
Time Frame: Change from baseline to 8 weeks
Knee extensor muscle strength measured isometrically
Change from baseline to 8 weeks
Change in Chair rise time
Time Frame: Change from baseline to 8 weeks
Time taken to get up and down from a chair 5 times
Change from baseline to 8 weeks
Change in balance
Time Frame: Change from baseline to 8 weeks
Ability to stand for 10 seconds in full tandem, semi-tandem and feet together
Change from baseline to 8 weeks
Change in gait speed
Time Frame: Change from baseline to 8 weeks
Time taken to walk 4 metres at a normal walking pace
Change from baseline to 8 weeks
Basal muscle protein synthesis
Time Frame: 0-3 hours
Muscle protein synthesis measured from 0-3h after an overnight fast
0-3 hours
Change in Erythrocyte fatty acid profile
Time Frame: Change from baseline to 8 weeks
Erythrocyte fatty acid profile
Change from baseline to 8 weeks

Collaborators and Investigators

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

Collaborators

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)

May 25, 2025

Study Completion (Actual)

May 25, 2025

Study Registration Dates

First Submitted

March 7, 2023

First Submitted That Met QC Criteria

March 7, 2023

First Posted (Actual)

March 17, 2023

Study Record Updates

Last Update Posted (Actual)

April 29, 2026

Last Update Submitted That Met QC Criteria

April 27, 2026

Last Verified

April 1, 2026

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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