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Effects of Omega-3 and Whey Protein Supplementation on Lean Mass in Older Adults

Effects of Omega-3 and Whey Protein Supplementation on Lean Mass and Strength Gains in Older Adults Performing Resistance Exercise: A Randomized, Double-Blind and Placebo-Controlled Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05862779
Acronym
W-3 and Whey
Enrollment
80
Registered
2023-05-17
Start date
2024-07-30
Completion date
2026-05-31
Last updated
2024-10-16

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

Conditions

Sarcopenia

Brief summary

To evaluate the effect of omega-3 supplementation combined with whey protein intake on lean mass and strength gains in older adults performing resistance exercise. Participants will be randomized into the 4 groups. The placebo group will receive 4 g per day of corn oil and 40 g per day of maltodextrin. The omega 3 + placebo group will receive 4 g per day of fish oil and 40 g per day of maltodextrin. The whey protein + placebo group will receive 40g per day of whey and 4g per day of corn oil. The omega 3 + whey group will receive 4g per day of fish oil and 40g per day of protein. All will perform the same exercise protocol for 12 weeks

Interventions

DIETARY_SUPPLEMENTPlacebo Group

The placebo group will receive 4 g per day of corn oil and 40 g per day of maltodextrin.

DIETARY_SUPPLEMENTWhey Protein + Placebo

The whey protein + placebo group will receive 40g per day of whey and 4g per day of corn oil.

DIETARY_SUPPLEMENTOmega 3 + Placebo

The omega 3 + placebo group will receive 4 g per day of fish oil and 40 g per day of maltodextrin.

DIETARY_SUPPLEMENTOmega 3 + Whey Protein

The omega 3 + whey group will receive 4g per day of fish oil and 40g per day of protein.

Sponsors

Federal University of Uberlandia
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
60 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Postmenopausal women (at least 1 year of menstrual interruption, self-reported); * To be able to practice strength exercises; * To be able to carry out supplementation; * Do not present physical, orthopedic or cardiovascular complications that prevent the performance of physical exercises; * No history of stroke or acute myocardial infarction; * Not being a smoker and/or alcoholic; * Do not perform hormone replacement therapy; * Do not use anti-inflammatory drugs; * To have normal kidney function; * To submit a medical certificate of health that proves that the individual is able to perform exercises.

Exclusion criteria

* Do not provide the necessary information for the development of the study; * Individuals with diseases previously diagnosed and undergoing treatment, such as type II diabetes mellitus, cancer, rheumatoid arthritis, high blood pressure, dyslipidemia, cardiovascular, and kidney and/or liver diseases.

Design outcomes

Primary

MeasureTime frame
Changes in lean mass (kg) using ultrasound and electrical bioimpedance in postmenopausal womenup to 12 weeks

Secondary

MeasureTime frame
Changes in strength (kg) using dynamometer in postmenopausal womenup to 12 weeks

Countries

Brazil

Contacts

Primary ContactErick P de Oliveira, PhD
erick_po@yahoo.com.br+5534 3225-8584
Backup ContactErick P de Oliveira, PhD
erick_po@yahoo.com.br+5514997273137

Outcome results

None listed

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