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Krill Oil and Resistance Exercise in Older Adults

The Effects of Krill Oil Supplementation on Adaptations in Muscle Strength, Function, Mass and Neuromuscular Function to a Pragmatic Home-based Resistance Exercise Intervention in Sedentary Older Adults: a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05869513
Acronym
KOREA
Enrollment
60
Registered
2023-05-22
Start date
2023-05-05
Completion date
2024-02-01
Last updated
2025-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sarcopenia

Keywords

Home exercise, Resistance exercise, Exercise, Krill oil, Muscle strength, Neuromuscular function, Physical function

Brief summary

The aim of this study is to determine whether krill oil supplementation enhances effects of a pragmatic resistance exercise programme on adaptations in muscle strength, mass, function and neuromuscular function in sedentary older adults. Hypothesis - krill oil supplementation will enhance the beneficial effects of resistance exercise on muscle strength, function, mass and neuromuscular function in sedentary older adults.

Interventions

DIETARY_SUPPLEMENTVegetable oil

Mixed vegetable oil

DIETARY_SUPPLEMENTKrill oil

Superba Krill Oil

OTHERHome-based resistance exercise

Home based resistance band and body weight exercise

Sponsors

University of Glasgow
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

All supplements will be matched for taste and look

Intervention model description

1:1 parallel group design

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Over the age of 60 years * scoring a low level of physical activity based on international physical activity questionnaire (not meeting the recommend physical activity which is at least 600 MET-min 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) * on anticoagulant therapy * allergies to seafood * regular consumption of more than 1 portion of oily fish per week * already taking fish or krill oil or other n3 PUFA supplements * femoral neck fracture or other severe of hip or knee operations * stroke * Parkinson's disease * COPD * kidney disease * hyperlipidaemia * obesity * osteoporosis.

Design outcomes

Primary

MeasureTime frameDescription
Nueromuscular Junction (NMJ) transmission instabilityChange from baseline to 16 weeksNMJ transmission instability will be measured by iEMG

Secondary

MeasureTime frameDescription
30s chair stand testChange from baseline to 16 weeksmeasuring the functional abilities
Gait speedChange from baseline to 16 weeksmeasuring the functional abilities
Force steadiness during submaximal isometric knee extensor contractionsChange from baseline to 16 weeksSteadiness of force whilst contracting
Knee extensor maximal torqueChange from baseline to 8 16 weeksKnee extensor maximal torque will be measured by a load cell
Grip strengthChange from baseline to 16 weeksGrip strength will be measured by handgrip dynamometer
Muscle thicknessChange from baseline to 16 weeksVastus Lateralis muscle thickness will be measured by ultrasound
Red Blood Cell Omega-3 levelsChange from baseline to 16 weeks

Other

MeasureTime frameDescription
Stance (%GC)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Step/ Extremity RatioChange from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Toe In / Out (deg)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Distance (cm)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Ambulation Time (sec)Change from baseline to 16 weeks
Velocity (cm/sec)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Step Time (sec)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Number of StepsChange from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Cadence (Steps/Min)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Step Time Differential (sec)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Step Length Differential (cm)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Cycle Time Differential (sec)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Mean Normalized VelocityChange from baseline to16 weeksMeasured during a 4m walk using a gaitrite mat
Cycle Time (sec)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Step Length (cm)Change from baseline to16 weeksMeasured during a 4m walk using a gaitrite mat
Stride Length (cm)Change from baseline to16 weeksMeasured during a 4m walk using a gaitrite mat
H-H Base Support (cm)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Single Support (%GC)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Double Support (%GC)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat
Swing (%GC)Change from baseline to 16 weeksMeasured during a 4m walk using a gaitrite mat

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026