Epigenetic Optimization Through Biofrequency Nutrition
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Personalized Nutritional Follow-Up.
- Who it may be relevant to
- Registry conditions: Nutrition Habits, Biomarkers / Hair, Epigenetic. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Functional Epigenetic Optimization Through Biofrequency-Guided Nutrition: A Randomized Controlled Trial
Overview
Biomarker-based nutrition has demonstrated superior efficacy compared to population-level approaches in improving health outcomes. Biofrequency analysis, a non-invasive technique based on the detection of electromagnetic vibrational patterns in hair follicles, offers a promising avenue for rapid functional assessment of nutritional status and epigenetic signals without reliance on blood or urine sampling. First, to evaluate the effect of a 90-day biofrequency-guided nutritional intervention on functional epigenetic status, as reflected in changes in the optimization report generated by the S-Drive system; second, to assess changes in adherence to the Mediterranean diet, anthropometric indicators, movement behaviors, and psychological well-being. Methods: In this randomized controlled trial, adults from a Sport Team from Region of Murcia (Spain) will be allocated to an experimental group receiving individualized lifestyle recommendations based on S-Drive biofrequency analysis and to a control group with no intervention. Participants in the experimental arm will apply tailored dietary guidance over 90 days. Conclusion: This study will generate foundational evidence on the utility of biofrequency technology for precision nutrition. If positive, the findings may inform scalable, low-risk strategies for personalized dietary interventions in preventive and community health settings.
Interventions
- Behavioral Personalized Nutritional Follow-Up
Participants in the experimental arm will receive a individual nutritional follow-up based on their epigenetic hair analysis results. This includes dietary guidance, recommendations tailored to genetic markers, and periodic consultations with a nutritionist over 4 weeks and continuous availability to clarify doubts via email . The aim is to evaluate changes in genetic expression or health biomarkers after the intervention period.
Primary outcome measures
- Change in biofrequency-derived epigenetic markers related to nutritional metabolism [Time frame: baseline and after 12-weeks post-intervention]
- Adherence to the Mediterranean Diet measured by the 14-item PREDIMED questionnaire [Time frame: Baseline and after 12 weeks of intervention]
Eligibility criteria
Inclusion criteria
- Age between 18 and 65 years.
- Active member of a registered athletics club.
- Willingness to provide a hair sample for genetic analysis.
- Ability to understand and sign the informed consent form.
- Commitment to complete the nutritional follow-up (for the intervention group) and to respond to pre- and post-intervention questionnaires.
Exclusion criteria
- Prior medical diagnosis of a genetic disorder affecting nutritional metabolism.
- Current use of nutritional supplements or special diets prescribed for medical reasons.
- Participation in another clinical or nutritional study during the intervention period.
- Pregnancy or breastfeeding at the time of enrollment.
- Inability to attend baseline or post-intervention assessments.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07093242 · UALBIO2025/010