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Effect of Immunocal® With Exercise Versus Casein With Exercise on Aging Processes in Elderly Persons

Effect of the Cysteine-rich Whey Protein Isolate (Immunocal®) in Combination With Physical Exercise on Muscle Function, Body Composition and Inflammatory Cytokine Levels in Elderly Persons: A Randomized, Double-blind Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00935610
Enrollment
99
Registered
2009-07-09
Start date
2009-06-30
Completion date
2014-03-31
Last updated
2021-02-09

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

Conditions

Aging, Sarcopenia

Keywords

Elderly persons, Muscle function and strength, Body composition, Inflammatory cytokine levels, Cognitive functions, Cysteine-rich whey protein isolate, Immunocal, Resistance training, Improved muscle function, Improved quality of life, Aging processes, Quality of life

Brief summary

Aging is typically associated with a decrease in skeletal muscle mass and muscle function, which contributes decisively to disability in old age and to the loss of quality of life.Resistance exercise can increase muscle strength, function and mass in older adults. The primary aim of this study is to determine whether the combination of resistance training with a supplementation of a cysteine- rich whey protein isolate (Immunocal) compared to combination of resistance training with casein used as control (casein contains little cysteine) could have the potential to provide a synergic beneficial impact on muscle mass and function which could translate to an improved quality of life in elderly persons.

Interventions

DIETARY_SUPPLEMENTImmunocal

20 grams per day of Immunocal for 135 days.

DIETARY_SUPPLEMENTCasein

20 grams per day for 135 days

Sponsors

Immunotec Inc.
Lead SponsorINDUSTRY

Study design

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

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 65 or older * Estimated GFR above 45ml/min * Total bilirubin in the normal range (0.2 to 1.2 mg/dl) AST (10-35 U/L for women and 10-50 U/L for men). ALT equal to or less than 2.5 times the upper limit of normal * BMI between 18.5-29.9 (kg)/m2 * Sedentary (\< 2 hours of structured exercise)in the last 2 or 3 months * Based on investigator judgment according to current Canadian guidelines, medical conditions such as hypertension, diabetes and hyperlipidemia have to be stable and optimally controlled before the subject starts the study.

Exclusion criteria

* History of angioedema or allergic reactions to any compound used in this study. * Milk protein intolerance * Subjects currently using N-acetylcysteine, alpha-lipoic acid supplements, or dry whey protein supplements. * Major surgery in the year prior to testing * Acute coronary or vascular event within the last year or progressive angina * Stroke within the past 2 years * Neurologist and/or orthopedic limitations * Uncontrolled thyroid or pituitary disease * Medication which has a major affect on cognitive function * Signs of early dementia as assessed by Mini-Mental State Examination * Weight loss of more than 4kg(or more than 5% body weight) over last 6 months * Alcohol abuse * Medication which interferes with muscle mass i.e. (corticosteroids) * Any life threatening conditions based on Investigator judgment. * Subjects with allergies/intolerance to soya. * Subjects currently undergoing immunosuppressive therapy.

Design outcomes

Primary

MeasureTime frame
The mean of percent change in muscle strength based on leg press and chest press evaluation assessed by resistance training equipment45, 90, 135 days

Secondary

MeasureTime frame
Percent change in lean body mass evaluated by DEXA.40, 90 and 135 days
The change in the plasma concentrations of Tumor Necrosis Factor-alpha (TNF-alpha), interleukin-6 (IL-6), C-reactive protein (CRP), glutathione, cysteine, asparagine, leucine and albumin40, 90 and 135 days
The clinical assessment of subject performance status (Quality of life and cognition, Physical Performance Test (PPT)).40, 90 and 135 days
The mean of percent change in muscle strength based on hand-grip dynamometer45, 90 and 135 days
The % change in body weight.40, 90 and 135 days
Bone mass density40, 90 and 135 days
6-min walk test40, 90 and 135 days
Insulin sensitivity evaluated by fasting plasma glucose and insulin (HOMA-IR model).40, 90 and 135 days

Countries

Canada

Outcome results

None listed

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