Introduction
At Lionheart Longevity, we believe that any consideration of travel for out-of-U.S. care should begin with a thoughtful conversation, clear information, and respect for patient choice.
For individuals interested in visiting a participating practitioner within the Lionheart Trusted Clinician Network at an out-of-U.S. location, the process begins with a Zoom call focused on trust-building, education, and determining whether participation in an applicable study, protocol, or evaluation process may be appropriate.
Lionheart Longevity provides non-medical coordination support for travel and logistics. Medical decisions are handled by the licensed clinician and site.
Step 1: Introductory Zoom Call
Your first step is a private Zoom conversation with a Lionheart Longevity care coordination representative.
This introductory call is intended to:
- help you understand the general process
- discuss your goals and interests
- explain available out-of-U.S. locations and participating practitioners
- review whether you may wish to be considered for a study, protocol, registry, or other clinician-directed program
- explain next-step requirements, including medical review and informed consent
This call is not a medical consultation, does not create a physician-patient relationship, and does not guarantee acceptance into any study, protocol, or clinical program.
Step 2: Study Participation and Eligibility Review
For many advanced regenerative, bioelectric, wellness, and longevity-oriented interventions available through participating out-of-U.S. sites, it is necessary for the individual to be considered for study participation, structured data collection, or a clinician-supervised protocol before proceeding.
Participation may require:
- submission of medical history and prior records
- review by the participating clinician or site
- confirmation that the individual meets inclusion criteria, if applicable
- discussion of alternatives, limitations, and uncertainties
- execution of a formal informed consent
- acknowledgement that results cannot be guaranteed
Not every individual will qualify. Participation is always subject to clinician review, site requirements, safety considerations, and local legal and regulatory frameworks.
Step 3: Informed Consent is Required
Before any study-related procedure, protocol-based care, or site-specific intervention is provided, the patient must receive and sign an appropriate informed consent document from the participating provider or study site.
Informed consent is important because it helps ensure that each patient understands, to the extent applicable:
- the nature of the study, protocol, or proposed intervention
- potential risks, discomforts, and burdens
- possible benefits, if any
- alternatives that may exist
- follow-up expectations
- privacy and data collection practices, if applicable
- the voluntary nature of participation
Patients should take the time needed to review all consent materials carefully and ask questions directly to the treating provider or study personnel before making a decision.ntary participation
Step 4: Travel, Hotel, and Clinic Logistics Support
If an individual is accepted by a participating site and chooses to proceed, Lionheart Longevity may provide concierge-style non-medical coordination to help make the visit more organized and less stressful.
This support may include:
- helping coordinate scheduling windows with the site
- sharing hotel options near the clinic
- assisting with trip timing and local transportation planning
- helping align travel dates with evaluation and follow-up appointments
- providing a clear coordination contact for non-medical logistics questions
Lionheart Longevity does not provide air travel, does not act as a travel agency, and does not make medical decisions on behalf of the treating clinic or practitioner.
Step 5: Independent medical judgment remains with the treating clinician
All medical care is provided only by the participating licensed practitioner or site. Each participating clinician exercises independent medical judgment and is solely responsible for patient evaluation, suitability determinations, study enrollment decisions, informed consent, treatment decisions, follow-up recommendations, and applicable recordkeeping.
Lionheart Longevity’s role is limited to education, introductions, and non-medical coordination support.
Important Disclosures
Lionheart Longevity does not guarantee outcomes, symptom improvement, eligibility, acceptance into any study, or access to any specific intervention.
Out-of-U.S. therapies, procedures, protocols, and study frameworks may not be reviewed, cleared, or approved by the U.S. Food and Drug Administration for any particular use.
Some offerings may be investigational, study-related, wellness-oriented, or available under local medical practice standards outside the United States.
Patients are encouraged to consult with their personal physician and other appropriate advisors before making travel or healthcare decisions.
A Careful and Respectful Way to Begin
We believe the best care journeys begin with transparency, patient choice, and informed decision-making.
That is why the process starts with a trust-building Zoom call, continues through eligibility review, and requires formal informed consent before any study participation or site-based intervention can proceed.
Request an Introductory Zoom Call
To learn more about non-medical coordination support for visiting a participating practitioner in the Lionheart Trusted Clinician Network at an out-of-U.S. location, request an introductory Zoom call today.
All participation is subject to clinician review, study or protocol requirements where applicable, and informed patient consent. Most OUS therapies require qualifying to enter a clinical study.
Disclaimer: Lionheart Longevity is not a hospital, does not practice medicine, and does not provide medical advice through this page. Lionheart Longevity provides education, introductions, and non-medical coordination support only. Any medical services are provided solely by independent licensed practitioners or study sites. Participation in any study, protocol, or intervention is voluntary and requires appropriate informed consent.