Texta Consulting Group
Where Human Experience
meets Scientific Validation
We help wellness innovators, therapeutic developers, and mission-driven organizations bring scientific clarity to what truly helps people regulate, recover, and grow.
From study design to publication, we build and execute rigorous clinical validation pathways so your product, program, or modality can make credible, compliant, and compassionate claims supported by real data.
Wellness is rich in innovation—and fragmented in evidence.
Across industries, programs, products, and digital platforms are helping people sleep better, move more, connect deeply, and regulate stress. Each gathers valuable information such as sensor data, survey results, or clinical notes; however, these pieces often live in isolation.
When data, experience, and interpretation remain separated, progress becomes partial: systems react to signals, but don’t understand context.
At TEXTA, we unify those dimensions through what we call the Context-to-Action Framework—a continuous, reflexive loop that merges three sources of knowledge: Empirical data, Subjective self-report & Interpretive insight.
This integration transforms information into insight and insight into action: creating evidence that is both scientifically sound and humanly relevant.
WHAT WE DO & HOW WE WORK
From framework to fieldwork
We design and run scientifically rigorous studies that turn your intervention—whether it’s a supplement, digital platform, behavioral program, or experiential retreat—into credible, publishable evidence of human regulation.
Everything we do is built on our Context-to-Action Framework, ensuring every project captures what’s measurable, meaningful, and interpretable in one continuous loop.
Our Process
I. Discovery & Alignment
We begin by understanding your intention: the outcomes you believe in, the population you serve, and the claims you hope to make.
Together we clarify regulatory pathways (wellness, therapeutic, or investigational) and align on feasibility, ethics, and data integrity.
II. Protocol & Study Design
Using the Context-to-Action Framework, we integrate three evidence streams into every protocol:
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Empirical: EEG, HRV, sleep, movement, and behavioral metrics
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Subjective: validated self-report instruments and contextual diaries
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Interpretive: clinician or researcher insight captured through structured qualitative methods
This triad defines our endpoints and analysis plan, linking physiology, psychology, and lived experience.
III. Regulatory Readiness
Our CCRP-certified team prepares and submits IRB documentation, ensuring alignment with GCP, HIPAA, and applicable NIH/FDA standards: so studies are ethically sound and defensible from day one.
IV. Execution & Oversight
We coordinate participant recruitment, site operations, and monitoring.
Our oversight model emphasizes transparency, safety, and fidelity while maintaining the human connection that underpins reliable data.
V. Analysis & Synthesis
Data alone is inert; insight emerges through interpretation.
We merge physiological patterns with participant narratives, identifying convergences that reveal how an intervention shapes regulation, resilience, and connection.
VI. Publication & Dissemination
Results are formatted for peer-review, white-paper, or investor-ready delivery.
Our manuscripts emphasize both quantitative outcomes and qualitative meaning, communicating findings in language that clinicians, regulators, and the public can trust.
Our Guiding Principles
Integration over
Isolation
Every dataset, voice, and interpretation matters.
Transparency
over
Persuasion
We let data speak for itself.
Humanity
within
rigor
Participants are partners, not subjects.
Ethics
before
Exposure
No shortcuts, no selective reporting.
What Makes TEXTA Different
Traditional research organizations often isolate physiology from psychology, or clinical from experiential.
We build systems that listen to the whole human. In doing so, we produce evidence that is scientifically valid, emotionally resonant, and socially credible.
Our approach is adaptable across interventions.
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Non-invasive behavioral therapies
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Plant-based and natural compounds
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Digital therapeutics and immersive experiences
SCIENTIFIC & THEORETICAL FOUNDATION
Our work stands at the intersection of psychophysiology, behavioral science, and human experience.
We draw on contemporary theories that explain how people regulate stress, safety, and engagement—not through a single pathway, but through the constant dialogue between body, mind, and environment.
These frameworks guide how we design studies, choose metrics, and interpret outcomes within our Context-to-Action Framework.
Polyvagal Theory
Core Insight:
The ANS shifts among states of safety/activation/shutdown based on cues of connection or threat.
How it Informs Our Research:
We use EEG and HRV to observe these state transitions before and after exposure to a modality: whether a behavioral program, digital tool, or experiential intervention.
Embodied Cognition
Core Insight:
Thinking and emotion are shaped through movement and interaction with the physical world.
How it Informs Our Research:
Supports our inclusion of movement- and environment-based modalities—from endurance programs to immersive learning—as valid mechanisms for nervous-system regulation.
Social Baseline Theory
Core Insight:
Humans conserve energy and regulate stress more efficiently through social connection and trust.
How it Informs Our Research:
Justifies evaluating social and group-based programs using both qualitative interviews and physiological synchrony measures.
Flow Theory
Core Insight:
Optimal performance arises when challenge and skill balance, producing focus and absorption.
How it Informs Our Research:
Guides how we interpret EEG Alpha/Theta dynamics and subjective flow reports during high-engagement activities.
Together, these perspectives form the backbone of our research philosophy:
Human regulation is relational, embodied, and measurable.
Our stance
We are agnostic to the modality and devoted to the method.
If an approach is ethical, non-addictive, and aimed at restoring or enhancing regulation, we can design the science to validate it.
Our role is not to champion a product—but to let transparent data reveal what truly works.
How we apply this foundation
We use these frameworks not as dogma, but as design principles.
They ensure our studies capture multiple dimensions of change—biological, psychological, and social—so findings remain relevant across diverse modalities:
Each pathway is unified by a single aim, which is to generate credible, human-centered evidence of how people self-regulate and recover.
HOW WE HELP & WHY IT MATTERS
We don’t just validate products
—
We Validate Possibilities.
Evidence is not just a regulatory checkbox—it’s an act of respect.
It respects the people who participate, the professionals who deliver care, and the public who decide what to believe.
When we bring empirical data, lived experience, and interpretive insight into a continuous loop, we generate more than statistics. We create scientific narratives. Stories that regulators can verify, clinicians can understand, and people can feel.
Innovation matures through clarity, accountability, and compassion.
That’s what TEXTA stands for.
Wellness & Health Brands
You’ve built products that promote rest, recovery, and regulation.
We design the science that allows you to make credible, compliant wellness or therapeutic claims.
→ Result: defendable evidence that strengthens consumer trust and market position.
Digital Therapeutic Developers
Your platform collects data every day, but turning that data into clinical-grade evidence requires structure and oversight.
We integrate physiological sensing, user self-report, and interpretive analysis to produce outcomes that align with DTx and regulatory standards.
→ Result: readiness for FDA or CE pathways and investor confidence.
Behavioral & Experiential Programs
Team-based performance schools, endurance or movement-based interventions: these experiences transform people.
We quantify that transformation, combining EEG, HRV, and qualitative insight to demonstrate how participants regulate, connect, and grow.
→ Result: measurable proof that elevates your program from anecdotal to empirical.
Non-profits & Community Initiatives
Your mission is to help people heal from anxiety, depression, PTSD, or substance use.
We help you validate outcomes ethically and affordably, so your impact is visible to funders and the communities you serve.
→ Result: transparent data that attracts support and sustains trust.
What You Gain
Integrated Validation Report
A unified analysis that weaves together physiological, psychological, and qualitative outcomes. We demonstrate real-world efficacy in language that regulators and investors trust.
Publication-Ready Manuscript
A peer-review-formatted document complete with figures, tables, and references, enabling submission to journals, white-paper release, or investor documentation.
Clinical & Regulatory Readiness Pack
Comprehensive documentation including protocols, SOPs, monitoring logs, and consent templates, all aligned with IRB, FDA, and digital-therapeutic standards.
Communication Brief
A plain-language summary that translates complex data into compelling, ethical storytelling for media, stakeholders, and the public.
Let’s turn meaningful work into measurable impact.
You’ve built something that helps people feel better, think clearer, sleep deeper, or reconnect with themselves and others.
Now it’s time to show, with data and dignity, how and why it works.
At TEXTA, we partner with wellness innovators, digital therapeutics teams, and experiential leaders who are ready to take their mission to the next level—through science that honors both human experience and clinical rigor.
Together, we can design a study that not only meets regulatory and scientific standards, but also tells the story of transformation in a way that inspires trust.
Let’s build the evidence your work deserves.