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Effect of magnesium and omega 3 co-supplementation supplement in Sarcopenic Elderly

The effect of magnesium and omega 3 co-supplementation on muscle strength, physical performance, muscle mass, inflammation, and intrinsic capacity index in elderly with sarcopenia: A double-blind randomized placebo-control trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090822002365N30
Enrollment
66
Registered
2024-06-22
Start date
2024-07-22
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Condition 1: Sarcopenia. Condition 2: Intrinsic capacity. Muscle wasting and atrophy, not elsewhere classified

Interventions

Intervention 1: Intervention group: 33 elderly receive one tablet of 250 mg of magnesium supplement and 1000 mg of omega 3(120 mg EPA and 180 mg DHA) daily for 8 weeks each. Intervention 2: Control gr

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 84 Years

Inclusion criteria

Inclusion criteria: Complete and sign informed consent Age 60-84 years Diagnosis of possible sarcopenia according to update of Asian Working Group for Sarcopenia (AWGS) (hand grip strength less than 28 kg in men and less than 18 kg in women) Impaired intrinsic capacity according to the first step of ICOPE guidelines of the World Health Organization Required no or some support with self-care (feeding, bathing, dressing, toileting). Taking any supplements containing magnesium and omega-3 during the last 2 months Taking any supplements containing more than 100 mg magnesium

Exclusion criteria

Exclusion criteria: Acute cardiovascular diseases, acute infection, and acute cerebrovascular disease Severe cardiac, liver, kidney dysfunction, autoimmune Uncontrolled diabetes Dementia, Parkinsons disease, and mental illnesses unable to provide informed consent because of aphasia, deafness, and blindness Physically-handicapped, disability, and use of a wheelchair or walker Taking hormonal drugs smoking Acute illness (cold, corona and any other viral-bacterial-fungal disease) Taking steroidal and non-steroidal anti-inflammatory drugs, aminoglycoside antibiotics, laxatives and laxatives

Design outcomes

Primary

MeasureTime frame
Muscle strength. Timepoint: At the baseline and after 8 weeks of intervention. Method of measurement: Handgrip strength.;Muscle function. Timepoint: At the baseline and after 8 weeks of intervention. Method of measurement: Short Physical Performance Battery (SPPB).;Muscle mass. Timepoint: At the baseline and after 8 weeks of intervention. Method of measurement: Bioelectrical Impedance Analysis (BIA).;Inflammation. Timepoint: At the baseline and after 8 weeks of intervention. Method of measurement: The level of CRP and ESR in serum.;Intrinsic capacity index. Timepoint: At the baseline and after 8 weeks of intervention. Method of measurement: Short Physical Performance Battery (SPPB), Mini-mental state examination(MMSE), Patient Health Questionnaire-9(PHQ-9), WHISPER test, WHO simple eye chart, Mini nutritional assessment (MNA).

Secondary

MeasureTime frame
Frailty. Timepoint: At the baseline and after 8 weeks of intervention. Method of measurement: The Fried phenotype (FP).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Vafa

Iran University of Medical Sciences

vafa.m@iums.ac.ir+98 21 8670 4743

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026