- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05774444
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
Status
Completed
Conditions
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
-
-
-
Glasgow, 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
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.
Sponsor
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- KIPLING
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.
Clinical Trials on Hypertrophy
-
Nationwide Children's HospitalActive, not recruitingSurgery | Tonsillar Hypertrophy | Adenoid HypertrophyUnited States
-
Rhode Island HospitalCompletedChildren, Only | Tonsillar Hypertrophy | Adenoid HypertrophyUnited States
-
Nagoya UniversityUnknownHypertensive Left Ventricular HypertrophyJapan
-
Sohag UniversityNot yet recruitingLeft Ventricular Hypertrophy
-
Gaziosmanpasa Research and Education HospitalNot yet recruitingTonsillar Hypertrophy | Voice Disorders in Children | Adenoid HypertrophyTurkey (Türkiye)
-
Organon and CoCompleted
-
Istanbul UniversityWithdrawn
-
Seoul National University HospitalSamsung Medical Center; Chung-Ang University Hosptial, Chung-Ang University... and other collaboratorsCompletedTonsillar HypertrophyKorea, Republic of
-
Marymount UniversityUniversity of TehranCompleted
-
Pierre-Yves P LequeuxCompleted
Clinical Trials on Vegetable oil
-
Dasman Diabetes InstituteRecruiting
-
University of FloridaNational Institute on Aging (NIA)Completed
-
Baylor Research InstituteUltragenyx Pharmaceutical IncCompletedAdult Polyglucosan Body Disease | Glycogen Brancher Enzyme Deficiency | Glycogen Storage Disease Type IVFrance
-
Academia Sinica, TaiwanNational Taiwan University HospitalCompleted
-
University of GlasgowCompleted
-
Aker Biomarine Antarctic ASAtlantia Food Clinical TrialsUnknown
-
University of GlasgowCompletedSarcopeniaUnited Kingdom
-
University of ReadingCompletedCardiovascular Risk FactorUnited Kingdom
-
Academia Sinica, TaiwanNot yet recruiting