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Human Immunodeficiency Virus InfectionBRM4NCT02214173

The Effect of an Enhanced Rice Bran Nutritional Supplement in HIV

A study testing rice bran arabinoxylan compound (RBAC) in people with Human Immunodeficiency Virus Infection, run by University of Miami at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to investigate the effects of the nutritional supplement rice bran arabinoxylan compound (RBAC) on metabolic syndrome variables in persons living with HIV. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Human Immunodeficiency Virus Infection
What is being tested?
rice bran arabinoxylan compound (RBAC)
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
47 participants
Where
1 siteUnited States
Study dates
Jan 2015to Jun 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 or older
  • Confirmed HIV infection
  • CD4 T cell counts > 50/µl and < 250/µl
  • On a stable ART regimen (e.g., Kaletra-based) before (≤6 months) and during the intervention
  • Planning to maintain current medication during the course of the intervention
  • Not on any lipid-lowering agents for a minimum of 3 months before the enrollment
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  • Previous nutritional supplement usage of similar polysaccharide formula permitted, but current use must be stopped 2 weeks before and during trial
  • Interested in participating in a dietary supplement study
  • Willing to follow recommendations for participating in the study
  • Willing to not consume food, alcohol, caffeine, or stimulants (amphetamines) 12 hours before each assessment
  • Able to provide informed consent

Who cannot join

  • Currently enrolled in another research trial for similar investigative nutritional therapies
  • Known allergy to rice, rice bran, mushrooms, or related food products
  • Any gastrointestinal disorders that could lead to uncertain resorption of the study supplement
  • Other medical complications that might preclude one from participating in the study, i.e., recent heart attack or stroke or chronic kidney disease
  • Currently taking immunomodulatory medication, i.e., interferon
  • Currently taking chemotherapeutic agents
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  • Multiple drug resistance
  • Current smoker
  • Severe anemia or other medical condition that will not permit a safe blood draw
  • A bleeding disorder
  • A terminal illness
  • Women who are pregnant or are attempting conception, especially in the presence of a history of recurrent spontaneous abortion

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Miami Miller School of Medicine, Clinical Research Building, Department of Psychiatry & Behavioral Sciences

    Miami, Florida, 33136

Other trials in United States

About this study

Official title: The Effect of an Enhanced Rice Bran Nutritional Supplement on Metabolic Syndrome Variables in HIV

The purpose of this study is to investigate the effects of the nutritional supplement rice bran arabinoxylan compound (RBAC) on metabolic syndrome variables in persons living with HIV. The hypothesis is that there will be a significant improvement in metabolic syndrome and immune variables in HIV-positive participants in the intervention group compared to the control group.

Read the detailed description

The purpose of this study is to investigate the effects of Rice Bran Arabinoxylan Compound (RBAC) on metabolic syndrome variables in persons living with HIV (PLWH). This nutritional supplement is made from a water soluble extract of rice bran that has been partially hydrolyzed by the action of a natural enzyme complex extracted from Shiitake mushroom. Given that these micronutrients may be important for regulating the immune system and metabolizing glucose, the investigators will explore the impact of RBAC on metabolic syndrome (MetSyn) variables according to the National Cholesterol Education Program (NCEP) Adult Treatment Panel III guidelines (1) (fasting plasma glucose, waist circumference, high-density lipoprotein [HDL] cholesterol, triglycerides, and blood pressure), secondarily on additional atherogenic variables (total cholesterol, low-density lipoprotein [LDL] cholesterol, hip circumference, and body mass index) and immune functioning (CD4+ and CD8+) among 40 HIV+ adult (18+ years of age and over) patients on stable antiretroviral therapy (ART). Specifically, subjects will participate in a 6-month, two-group, randomized intervention, where one group (n=20) will take 3 gram/day RBAC and the other group (n=20) will take a placebo to compare differences in outcomes between the two groups. The results of the study are intended to address the multi-faceted physiological problems of HIV+ patients by testing the efficacy of a nutritional supplement intervention on multiple outcomes in this population.

No substantial psychological, medical, or social risks exist to the participants, other than minor discomfort associated with the venipuncture. 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 Institutional Review Board.

The components of RBAC 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. Potential adverse effects will be explained to each participant when informed consent is obtained. Whole foods supplements are virtually no different than consuming food, because of how they are manufactured. The investigators prior study on RBAC showed no adverse effects. 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. Study staff will provide additional follow-up and consultation with any subject who experiences an untoward side effect.

Other potential risks include:

  1. Randomization. A potential risk for the placebo group is no improvement in the investigators outcomes of interest.
  2. Data collection. The investigators foresee minimal risks associated with the testing, other than discomfort or fatigue.

A toxicology search for each component reveals no unique toxicity characteristic of the materials. As reported by Daiwa Health Development, the manufacturer of the product, thousands of people currently use RBAC (under the trade names BRM4 and PeakImmune 4), and Daiwa is unaware of significant toxicities. Daiwa applies the latest scientific methods to ensure the value and safety of their raw materials. Daiwa 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 these MetSyn and immune functioning variables 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 MetSyn variables and immune system functioning, but their long-term use has unknown consequences.

The information obtained in this study will help in determining the efficacy of using RBAC on MetSyn and metabolic variables and immune system functioning. By participating in the study, subjects may experience improved health status. The risk of participating in this study is reasonable because of the potential enhancements in metabolic and immune system functioning with improved nutritional status.

Being tested
rice bran arabinoxylan compound (RBAC), Placebo
Keywords
HIV, BRM4, hydrolyzed rice bran, metabolic syndrome
Medical subject headings
Acquired Immunodeficiency Syndrome, Metabolic Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • rice bran arabinoxylan compound (RBAC)Dietary supplement

    2 capsules with 6 to 8 ounces of water 3 times per day (6 tablets total per day) for 6 months.

  • PlaceboDietary supplement

    2 capsules with 6 to 8 ounces of water 3 times per day (6 tablets total per day) for 6 months.

Study groups in NCT02214173
Study groupRoleWhat they receive
rice bran arabinoxylan compound (RBAC)Experimental2 capsules with 6 to 8 ounces of water 3 times per day (6 tablets total per day) for 6 months.
Receives: Dietary Supplement: rice bran arabinoxylan compound (RBAC)
placeboPlacebo comparator2 capsules with 6 to 8 ounces of water 3 times per day (6 tablets total per day) for 6 months.
Receives: Dietary Supplement: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Improvement in Metabolic Syndrome Markers

    Improvement in glucose, lipid profile, blood pressure, cluster of differentiation 4 (CD4), and cluster of differentiation 8 (CD8) values.

    Measured: 3 months and 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Aug 2014 (estimated)
  2. Study startJan 2015
  3. Primary completionJun 2016
  4. Study completionJun 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
47 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02214173
Sponsor's protocol ID
20130279
Acronym
BRM4
Status last verified
Jul 2016
First submitted
1 Aug 2014
Last updated
18 Jul 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing rice bran arabinoxylan compound (RBAC) in people with Human Immunodeficiency Virus Infection, run by University of Miami at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Jul 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Improvement in Metabolic Syndrome Markers (time frame: 3 months and 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jul 2016.

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