NCT05869526

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
61

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2023

Completed
10 days until next milestone

First Submitted

Initial submission to the registry

May 11, 2023

Completed
11 days until next milestone

First Posted

Study publicly available on registry

May 22, 2023

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2024

Completed
Last Updated

March 30, 2025

Status Verified

March 1, 2025

Enrollment Period

9 months

First QC Date

May 11, 2023

Last Update Submit

March 25, 2025

Conditions

Keywords

muscle massstrengthomega-3ageing

Outcome Measures

Primary Outcomes (1)

  • Change in knee extensor maximal isometric torque ( MVC)

    Knee extensor maximal isometric torque measured during a maximal voluntary contraction

    Change from baseline to 16 weeks

Secondary Outcomes (9)

  • Change in fat mass

    Change from baseline to 16 weeks

  • Change in lean mass

    Change from baseline to 16 weeks

  • Blood sample

    Change from baseline to 16 weeks

  • Change in Grip strength

    Change from baseline to 16 weeks

  • Change in Muscle thickness

    Change from baseline to 16 weeks

  • +4 more secondary outcomes

Other Outcomes (20)

  • Step Time (Sec)

    Change from baseline to 16 weeks

  • Cycle Time (Sec)

    Change from baseline to 16 weeks

  • Step Length (CM)

    Change from baseline to 16 weeks

  • +17 more other outcomes

Study Arms (3)

Fish oil

ACTIVE COMPARATOR

Fish oil 4 g/day

Dietary Supplement: Fish oil

Krill oil

ACTIVE COMPARATOR

Krill oil 4g/day

Dietary Supplement: Kril oil

Placebo

PLACEBO COMPARATOR

Vegetable oil 4g/day

Dietary Supplement: Vegetable oil

Interventions

Fish oilDIETARY_SUPPLEMENT

EPA rich fish oil

Fish oil
Kril oilDIETARY_SUPPLEMENT

Superba Krill Oil

Krill oil
Vegetable oilDIETARY_SUPPLEMENT

Mixed vegetable oil

Placebo

Eligibility Criteria

Age60 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stuart Robert Gray

Glasgow, Scotland, United Kingdom

Location

MeSH Terms

Conditions

Sarcopenia

Interventions

Fish OilsPlant Oils

Condition Hierarchy (Ancestors)

Muscular AtrophyNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesAtrophyPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsSigns and Symptoms

Intervention Hierarchy (Ancestors)

OilsLipidsPlant PreparationsBiological ProductsComplex Mixtures

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
Supplements will be identical in look and taste
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: 1:1:1 basis
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

May 11, 2023

First Posted

May 22, 2023

Study Start

May 1, 2023

Primary Completion

February 1, 2024

Study Completion

April 1, 2024

Last Updated

March 30, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

Locations