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Oxidative Stress Links Aging, Activity, and Mobility Limitation

Oxidative Stress Links Aging, Activity and Mobility Limitation

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01177189
Enrollment
87
Registered
2010-08-06
Start date
2011-07-01
Completion date
2017-07-03
Last updated
2019-02-21

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

Conditions

Aging

Keywords

Oxidative Stress, Free radicals, Aging

Brief summary

The purpose of this study is to understand why and how oxidative stress negatively impacts mobility in the elderly, and to determine whether antioxidant supplements can increase vascular health and mobility.

Detailed description

With the premise that U.S. Veteran demographics reveal an aging population with significant mobility limitation and oxidative stress is tightly linked to both of these characteristics, a series of skeletal muscle/vascular studies are proposed. Specifically, in a series of recent studies the investigators' group has documented positive vascular consequences of antioxidant supplementation during exercise in older subjects that negatively impacted young people. Further provocative findings revealed that following exercise training the older subjects were now also negatively impacted by the antioxidant supplementation. These findings have implications for the understanding of the complex balance between the positive effects of exercise-based rehabilitation, exercise induced oxidative stress, aging, frailty, and subsequent mobility limitation. Therefore four specific aims are proposed that will answer the questions of where (I) oxidative stress is most prevalent in the elderly, why (II) oxidative stress occurs in the elderly, what (III) are the acute consequences of oxidative stress in the elderly, and finally how (IV) can exercise-induced oxidative stress as the result of exercise training in elderly be appropriately managed with exogenous antioxidant therapy to promote compliance and the positive outcome of increased mobility.

Interventions

DIETARY_SUPPLEMENTVitamins C, E, and alpha lipoic acid

Oral antioxidant cocktail or placebo to be consumed daily

Sponsors

University of Utah
CollaboratorOTHER
VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Intervention model description

Participants will consume either a daily oral antioxidant cocktail or a placebo. The oral antioxidant cocktail consists of vitamin C, vitamin E, and alpha lipoic acid.

Eligibility

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

Inclusion criteria

* Healthy men and women aged either between 18 - 30 years (young group) and \>70 years (old group) * Free of overt disease. Subjects will be non-obese (BMI \< 30) and have plasma glucose concentrations \< 7.0 mmol/L under fasting conditions and \< 11.1 mmol/L at 120 minutes of an oral glucose tolerance test (OGTT) * Subjects will be sedentary, defined here as no regular physical activity for at least the prior 2 years * Candidates must have no orthopedic limitations that would prohibit them from performing cycle or knee-extensor exercise * All women will be postmenopausal (either natural or surgical) defined as a cessation of menses for at least 2 years, and in women without a uterus, follicle stimulating hormone (FSH) \> 40 IU/L

Exclusion criteria

* Candidates demonstrating dyslipidemia based on the National Cholesterol Education Program Guidelines of plasma total cholesterol \> 240 mg/dl with LDL-cholesterol \> 160 mg/dl will be excluded from participation * Candidates who smoke or are taking medications (blood pressure medications, statins, antioxidants etc.) that could influence the results of the study will not be eligible * In terms of diet, subjects will be asked to maintain a dietary record for one week prior to the pre-screening and if this reveals a diet that differs substantially from the typical average diet in both the young and old, the subject will not be eligible * Women currently taking hormone replacement therapy (HRT) in the preceding year will be excluded from the proposed studies

Design outcomes

Primary

MeasureTime frameDescription
Vascular Function (i.e. % Flow Mediated Vasodilation)8 weeksThe effect on flow mediated vasodilation is measured using Doppler ultrasound.

Secondary

MeasureTime frameDescription
Exercise-induced Oxidative Stress (i.e. Free Radical Concentrations and Levels of Lipid Peroxidation)8 weeksFree radicals and levels of lipid peroxidation were measured using electron paramagnetic spectroscopy and ELISA assays. A minimum value is 0 and a maximum value is 10. A higher value is a worse outcome.
Vascular Function Following the Antioxidant Intervention8 weeksThe degree of vasodilation following the antioxidant intervention measured by Doppler ultrasound.

Participant flow

Participants by arm

ArmCount
Arm 1
Young healthy men and women aged 18-30 Vitamins C, E, and alpha lipoic acid: Oral antioxidant cocktail or placebo to be consumed daily
42
Arm 2
Older healthy men and women aged \>70. Vitamins C, E, and alpha lipoic acid: Oral antioxidant cocktail or placebo to be consumed daily
45
Total87

Baseline characteristics

CharacteristicArm 2TotalArm 1
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
45 Participants45 Participants0 Participants
Age, Categorical
Between 18 and 65 years
0 Participants42 Participants42 Participants
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United States
45 Participants87 Participants42 Participants
Sex: Female, Male
Female
17 Participants38 Participants21 Participants
Sex: Female, Male
Male
28 Participants49 Participants21 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 420 / 45
other
Total, other adverse events
0 / 420 / 45
serious
Total, serious adverse events
0 / 420 / 45

Outcome results

Primary

Vascular Function (i.e. % Flow Mediated Vasodilation)

The effect on flow mediated vasodilation is measured using Doppler ultrasound.

Time frame: 8 weeks

ArmMeasureValue (MEAN)Dispersion
Arm 1Vascular Function (i.e. % Flow Mediated Vasodilation)7.4 percentage of vasodilationStandard Error 0.6
Arm 2Vascular Function (i.e. % Flow Mediated Vasodilation)5.2 percentage of vasodilationStandard Error 0.4
Secondary

Exercise-induced Oxidative Stress (i.e. Free Radical Concentrations and Levels of Lipid Peroxidation)

Free radicals and levels of lipid peroxidation were measured using electron paramagnetic spectroscopy and ELISA assays. A minimum value is 0 and a maximum value is 10. A higher value is a worse outcome.

Time frame: 8 weeks

ArmMeasureValue (MEAN)Dispersion
Arm 1Exercise-induced Oxidative Stress (i.e. Free Radical Concentrations and Levels of Lipid Peroxidation)1.51 units on a scaleStandard Error 0.19
Arm 2Exercise-induced Oxidative Stress (i.e. Free Radical Concentrations and Levels of Lipid Peroxidation)2.7 units on a scaleStandard Error 0.13
Secondary

Vascular Function Following the Antioxidant Intervention

The degree of vasodilation following the antioxidant intervention measured by Doppler ultrasound.

Time frame: 8 weeks

ArmMeasureValue (MEAN)Dispersion
Arm 1Vascular Function Following the Antioxidant Intervention5.8 percentage of vasodilationStandard Error 0.6
Arm 2Vascular Function Following the Antioxidant Intervention8.2 percentage of vasodilationStandard Error 0.6

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