Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation Research

NCT ID: NCT04806620

Last Updated: 2026-01-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

10000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-07-05

Study Completion Date

2030-12-31

Brief Summary

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The unhide® Project is a non-interventional, longitudinal research study designed to establish a secure data repository of demographic, health, and lifestyle information from individuals with brain inflammation and related neuroinflammatory conditions. Participants in the United States aged 2 years and older will provide self-reported health data, biometrics, and symptom diaries through the MyDataHelps™ app (branded as unhide® for this study). The goal is to create comprehensive longitudinal profiles to facilitate research into disease subtypes, causes, diagnostics, and potential treatments, as well as to identify potential participants for future optional studies. "Healthy" individuals without brain inflammation are also eligible to participate.

The digital health research platform used in this study was originally developed and designed by Solve M.E and was called SolveTogether. The Brain Inflammation Collaborative (BIC) expanded upon Solve M.E.'s work to include related diagnoses, pediatric participants, enhance symptom tracking, and more. BIC and Solve M.E. combined Solve Together and unhide®, to create The unhide® Solve Together Unified Platform in 2025.

Detailed Description

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The unhide® Project is sponsored by the Brain Inflammation Collaborative (BIC), a nonprofit organization dedicated to advancing understanding, diagnosis, and treatment of neuroinflammatory illness. This study will create a secure, long-term repository of demographic, health, lifestyle, biometric, and symptom data from individuals in the United States with brain inflammation and related conditions, as well as unaffected individuals. Data will be collected remotely through MyDataHelps™ by Care Evolution (rebranded as unhide®), a secure mobile and web-based platform enabling eConsent, survey completion, health record linkage, and optional symptom/activity tracking.

Eligible participants are U.S. residents aged 2 years and older, including both self-identified and physician-diagnosed individuals with infection-associated, autoimmune, neuroimmune, inflammatory gastrointestinal, and behavioral/mood disorders, as well as "healthy" individuals. There are minimal exclusion criteria: individuals living outside the U.S., wards of the state, and those with decisional impairment are ineligible. Pregnant women may participate, and prior or concurrent participation in other research studies is permitted.

The study will follow participants for 10 or more years, collecting self-reported health information, comorbidities, medical history, biometrics (e.g., heart rate, sleep, activity), and symptom data to generate comprehensive longitudinal health profiles. This data resource aims to accelerate translational research, identify disease subtypes, uncover causes and risk factors, support the development of diagnostic tests and treatments, and improve outcomes for individuals affected by neuroinflammation.

Conditions

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Post-Acute COVID-19 Syndrome ME/CFS Rheumatic Arthritis Juvenile Rheumatoid Arthritis (JRA) Psoriatic Arthritis (PsA) Ankylosing Spondylitis (AS) Autoimmune Encephalitis Celiac Disease Celiac Disease in Children Chronic Lyme Disease Post-treatment Lyme Disease Syndrome Crohn's Disease Dysautonomia Anorexia Nervosa Bulimia Nervosa ARFID Avoidant / Restrictive Food Intake Disorder Ehlers Danlos Syndrome Endometriosis Fibromyalgia (FM) Long COVID Lupus Migraines Mast Cell Activation Syndrome Multiple Sclerosis Myalgic Encephalomyelitis (ME) Myasthenia Gravis, Generalized Myasthenia Gravis in Children Narcolepsy Obsessive Compulsive Disorder (OCD) PANDAS Pediatric Acute-onset Neuropsychiatric Syndrome (PANS) POTS - Postural Orthostatic Tachycardia Syndrome General Anxiety Disorder, Social Anxiety Disorder PTSD - Post Traumatic Stress Disorder Psoriasis Traumatic Brain Injury Tourette's Syndrome Inflammatory Bowel Disease (IBD) Autoimmune Diseases Neurological Diseases or Conditions Psychiatric Disorder Sjogren's Syndrome Ulcerative Colitis and Crohn's Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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People with brain inflammation and related neuroinflammatory conditions

No intervention will be administered.

No interventions assigned to this group

Healthy Controls

No intervention will be administered.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

Participants may be either self-diagnosed, or diagnosed by a physician with the following conditions:

* Infection-associated chronic conditions such as Long COVID, chronic Lyme, myalgic encephalomyelitis (ME/CFS), and post-acute neuropsychiatric syndrome (PANS/PANDAS).
* Neuroimmune, developmental, autonomic, and neurological conditions like migraines, dysautonomia, POTS, multiple sclerosis, and autism spectrum disorder.
* Autoimmune diseases such as Lupus, Sjogren's Disease, rheumatoid arthritis, myasthenia gravis, ankylosing spondylitis, and related autoimmune conditions.

Inflammatory gastrointestinal conditions such as Crohn's Disease, Celiac Disease, and ulcerative colitis.

* Behavioral and mood disorders such as anxiety, depression, bipolar disorder, PTSD, eating disorders, OCD, and other related conditions.
* "Healthy" people (without brain inflammation), including unaffected individuals, unaffected individuals in the same household, and unaffected individuals who are married to relatives and family members.
* Have consistent internet access and a cell phone, tablet, or PC since this is an online or app-based platform that requires entering data and completing surveys.
* Currently live in the United States
* Be able to participate in English (stay tuned for updates about the Spanish language version)
* Be willing to share symptom and health data through the platform
Minimum Eligible Age

2 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Solve ME/CFS Initiative

OTHER

Sponsor Role collaborator

Care Evolution

UNKNOWN

Sponsor Role collaborator

Columbia University

OTHER

Sponsor Role collaborator

Brain Inflammation Collaborative

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Megan L Fitzgerald, PhD

Role: PRINCIPAL_INVESTIGATOR

Brain Inflammation Collaborative

Locations

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Brain Inflammation Collaborative

Delafield, Wisconsin, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Megan L Fitzgerald, PhD

Role: CONTACT

1-833-286-4433

Christina Moon

Role: CONTACT

1-833-286-4433

Facility Contacts

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Christy Jagdfeld, CPA

Role: primary

833-286-4433

Christina Moon

Role: backup

833-286-4433

References

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Ramiller A, Mudie K, Seibert E, Whittaker S. The Facilitation of Clinical and Therapeutic Discoveries in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and Related Diseases: Protocol for the You + ME Registry Research Platform. JMIR Res Protoc. 2022 Aug 10;11(8):e36798. doi: 10.2196/36798.

Reference Type DERIVED
PMID: 35816681 (View on PubMed)

Other Identifiers

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1

Identifier Type: -

Identifier Source: org_study_id

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