Transparent, peer-reviewed research and measurable results from VitaWell's integrative health programs. We believe true wellness should be backed by science.
Explore our portfolio of rigorous studies evaluating the efficacy of our holistic interventions.
Participants in the VitaWell mindfulness protocol showed a 68% reduction in GAD-7 scores compared to 22% in the waitlist control group (p<0.001).
Published & ReplicatedSignificant improvement in HbA1c (-0.8%), CRP (-42%), and lipid profiles. 73% of participants achieved target metabolic health benchmarks.
Published & ReplicatedActigraphy data showed +54 min average total sleep time and +31% deep sleep ratio. PSQI scores improved from 14.2 to 5.1.
Published & Replicated38% improvement in sit-to-stand performance, reduced fall risk by 61%, and significant gains in sarcopenia screening metrics.
Under ReviewCAPS-5 scores decreased by 47% in the intervention group versus 18% in standard care. High adherence rate (89%).
Published & ReplicatedMetagenomic sequencing revealed +34% increase in SCFA-producing bacteria. Correlated with reduced bloating and improved energy levels.
Published & ReplicatedOur research and clinical operations meet rigorous international standards.
All clinical trials reviewed by independent Institutional Review Boards
End-to-end encryption and anonymized data handling
Interventions aligned with NIH complementary health standards
Information security management for clinical data
Selected articles from VitaWell researchers and clinical partners.
Dr. E. Chen, Dr. M. Rodriguez, et al. (2024). Vol 22, Issue 4, pp. 312-328. DOI: 10.1016/j.jim.2024.03.012
View Abstract →Dr. S. Mitchell, VitaWell Research Team. (2023). Vol 68, 101-115. DOI: 10.1016/j.smrv.2023.08.004
View Abstract →VitaWell Clinical Group. (2023). Frontiers in Psychology, Sec. Public Mental Health. DOI: 10.3389/fpsyg.2023.11204
View Abstract →How we collect, analyze, and report clinical data with transparency and ethics.
All interventions follow SOPs developed by our clinical advisory board. Inclusion/exclusion criteria, baseline assessments, and outcome measures are pre-registered on ClinicalTrials.gov.
We combine validated psychometric scales (PSQI, GAD-7, PHQ-9), biometric tracking (actigraphy, HRV, continuous glucose monitoring), and participant-reported outcomes for holistic data.
Informed consent is mandatory. Data is de-identified, encrypted at rest/transit, and stored on SOC2-compliant servers. Participants may withdraw anytime without penalty.
Transparent answers about our evidence, data privacy, and clinical standards.
Every study is pre-registered, IRB-approved, and follows CONSORT or STROBE reporting guidelines. We employ independent statisticians for data analysis and publish both positive and null results.
Never. We are strictly HIPAA and GDPR compliant. Your data is encrypted, anonymized for research, and never sold. You retain full ownership and can request deletion at any time.
We commit to open science. De-identified datasets and analysis code are uploaded to institutional repositories upon publication, in compliance with ethical and privacy standards.
All nutritional protocols follow FDA-compliant dosing guidelines. Our supplements are manufactured in NSF-certified facilities and undergo third-party testing for purity and potency.