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| Name | Class |
|---|---|
| CellHealth Institute | UNKNOWN |
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The investigators are conducting this research because they want to determine if a dietary supplement, called Everycell™, has an effect on the functioning of the study participants' cells. The results of this research will be used to help develop additional strategies for trying to fight the effects of aging. The primary purpose of this study is to determine the effectiveness of Everycell™ compared to placebo (a pill that does nothing) on DNA damage, inflammation, stress, and related factors. Taking Everycell™ is not a medical prescription, treatment, or cure for any known disease or condition.
Helping patients' nutritional status is important to prevent the continued worsening of chronic diseases and also to counteract the effects of aging. Americans also have difficulties with compliance to prescription medications due to their toxicity and side effects. This study aims to learn more about how a dietary supplement may improve nutritional status and enable the body to normalize cellular functioning, which may improve quality of life. The results of this research will be used to determine if Everycell™ is beneficial for overall cellular health and to counteract the effects of aging.
The proposed study is a 6-week, randomized, double-blind, placebo-controlled trial to evaluate the effect of everycell compared to placebo on DNA damage, inflammation, stress, and related factors in 30 healthy adults (18-55 years of age). Participants will be assessed at baseline, 4 weeks (end of intervention), and 6 weeks (2-week washout period), and the study will consist of two treatment arms, including: (a) Everycell and (b) placebo. Additionally, the study will examine subject health-related quality of life (QoL).
Specific Aim. Test the effect of Everycell compared to placebo on DNA damage, inflammation, stress, and related factors in a sample of healthy adults.
Hypothesis. The Everycell group will demonstrate improvements in DNA damage, inflammation, stress, and related factors at 4 and 6-week follow-ups compared to placebo.
Although all measures to protect confidentiality will be put in place, the possibility exists that electronic data could be jeopardized. In the remote case that such event occurs, it will be immediately reported to the IRB.
No substantial psychological, medical, or social risks exist to the participants, other than minor discomfort associated with the venipuncture. The components of everycell should be harmless without significant food allergies. No serious, untoward side effects have been reported to the company by consumers nor observed during previous human studies. If any side effect does occur, the remedy is to discontinue until asymptomatic, and then reintroduce at 1/4 dosage, increasing by the same amount every 2 days, if uneventful, until full dosage is achieved. A toxicology search for each component reveals no unique toxicity characteristic of the materials. As reported by CellHealth Institute, the manufacturer of the product, many customers currently use Everycell, and CellHealth Institute is unaware of significant toxicities.
CellHealth Institute applies the latest scientific methods to ensure the value and safety of their raw materials. CellHealth Institute products are manufactured in state-of-the-art facilities, under strict quality control and environmental protection standards.
Participants will incur no additional appreciable psychological or social risks by participating in this study, although they may undergo psychological and physical discomfort sometimes. The process of interviewing during the assessment may cause discomfort. Discomfort or fatigue may also be experienced in completing the assessment battery.
Alternatives to this study for improving DNA damage, inflammation, and stress include prescription medications, exercise, dietary modification, and other nutritional supplements. The risks of medications can be very significant, including life-threatening, but the risk of taking nutritional supplements is not totally understood, since they are not regulated by the US Food and Drug Administration. Medications and nutritional supplements, as part of a change in lifestyle behaviors, may also prove to be beneficial for DNA damage, inflammation, and stress, but their long-term use has unknown consequences.
The information obtained in this study will help in determining the efficacy of using a nutritional supplement for improving DNA damage, inflammation, and stress outcomes. By participating in the study, subjects may experience improved DNA damage, inflammation, and stress. The risk of participating in this study is reasonable because of the potential enhancements in DNA damage, inflammation, and stress with improved nutritional status.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Everycell™ | Experimental | Patient will take 1 tablet two times daily of Everycell™ (double-blind) for the 4-week treatment period. |
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| Placebo | Placebo Comparator | Patient will take 1 tablet two times daily of the placebo (double-blind) for the 4-week treatment period. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Everycell™ | Dietary Supplement |
| ||
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Change from Baseline in Nuclear factor kappa-light-chain-enhancer of activated B cells at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Fructosamine at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Protein Thiol Test at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Homocysteine at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Telomere Length at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Cluster of Differentiation 4 (Regulatory T-cell) at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) |
| Measure | Description | Time Frame |
|---|---|---|
| Change from Baseline in Systolic Blood Pressure at 4 weeks | Systolic and diastolic blood pressure measured. | Baseline, 4-week follow-up |
| Change from Baseline in Pulse at 4 weeks | Baseline, 4-week follow-up |
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Inclusion Criteria:
Be between the ages of 18 and 55
Live independently without medical assistance
Willing to provide informed consent to participate in the study
Willing to follow our procedures and requirements for the study, including:
Patients may take a similar dietary supplement as the one used in the study, but they must stop taking all similar dietary supplements 2 weeks prior to starting the study and for the 6 weeks duration of the study.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| John Lewis, Ph.D. | University of Miami | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Miami Miller School of Medicine, Clinical Research Building | Miami | Florida | 33136 | United States |
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| ID | Term |
|---|---|
| D000073893 | Sugars |
| ID | Term |
|---|---|
| D002241 | Carbohydrates |
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| Baseline, 4-week follow-up |
| Change from Baseline in Cluster of Differentiation 8 at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Cluster of Differentiation 56 (Natural Killer cell) at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in 8-hydroxydeoxyguanosine at 4 weeks | Urine sample for 8-OHdG and 8-epi-PGF-2-alpha | Baseline, 4-week follow-up |
| Change from Baseline in 8-epi-PGF-2-alpha at 4 weeks | Urine sample for 8-OHdG and 8-epi-PGF-2-alpha | Baseline, 4-week follow-up |
| Change from Baseline in Forkhead box protein 3 (Regulatory T-cell) at 4 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 4-week follow-up |
| Change from Baseline in Nuclear factor kappa-light-chain-enhancer of activated B cells at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Fructosamine at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Protein Thiol Test at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Homocysteine at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Telomere Length at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Cluster of Differentiation 4 (Regulatory T-cell) at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Cluster of Differentiation 8 at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Cluster of Differentiation 56 (Natural Killer cell) at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in 8-hydroxydeoxyguanosine at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in 8-epi-PGF-2-alpha at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Forkhead box protein 3 (Regulatory T-cell) at 6 weeks | Blood draw for NF-kB, fructosamine, protein thiol test, homocysteine, telomere length, and CD4/FoxP3 (regulatory T-cells), CD8, and CD56 (NK cell) | Baseline, 6-week follow-up |
| Change from Baseline in Waist Circumference at 4 weeks | Measure of body composition: waist circumference (cm). | Baseline, 4-week follow-up |
| Change from Baseline in Hip Circumference at 4 weeks | Measure of body composition: hip circumference (cm). | Baseline, 4-week follow-up |
| Change from Baseline in Weight at 4 weeks | Measure of body composition: weight. | Baseline, 4-week follow-up |
| Change from Baseline in Height at 4 weeks | Measure of body composition: height. | Baseline, 4-week follow-up |
| Change from Baseline in Body Mass Index at 4 weeks | Measure of body composition: height and weight to assess BMI. | Baseline, 4-week follow-up |
| Change from Baseline in International Physical Activity Questionnaire at 4 weeks | Baseline, 4-week follow-up |
| Change from Baseline in SF-36v2™ Health Survey at 4 weeks | Baseline, 4-week follow-up |
| Change from Baseline in Systolic Blood Pressure at 6 weeks | Systolic and diastolic blood pressure measured. | Baseline, 6-week follow-up |
| Change from Baseline in Diastolic Blood Pressure at 4 weeks | Systolic and diastolic blood pressure measured. | Baseline, 4-week follow-up |
| Change from Baseline in Diastolic Blood Pressure at 6 weeks | Systolic and diastolic blood pressure measured. | Baseline, 6-week follow-up |
| Change from Baseline in Pulse at 6 weeks | Baseline, 6-week follow-up |
| Change from Baseline in Waist Circumference at 6 weeks | Measure of body composition: waist circumference (cm). | Baseline, 6-week follow-up |
| Change from Baseline in Hip Circumference at 6 weeks | Measure of body composition: hip circumference (cm). | Baseline, 6-week follow-up |
| Change from Baseline in Weight at 6 weeks | Measure of body composition: weight. | Baseline, 6-week follow-up |
| Change from Baseline in Height at 6 weeks | Measure of body composition: height. | Baseline, 6-week follow-up |
| Change from Baseline in Body Mass Index at 6 weeks | Measure of body composition: height and weight to assess BMI. | Baseline, 6-week follow-up |
| Change from Baseline in International Physical Activity Questionnaire at 6 weeks | Baseline, 6-week follow-up |
| Change from Baseline in SF-36v2™ Health Survey at 6 weeks | Baseline, 6-week follow-up |