RecruitingNCT07213700

InRAD Observational Study

The International Registry for Alzheimer's Disease and Other Dementias (InRAD): An International Registry Observational Study Dedicated to Evaluating Outcomes Data in Alzheimer's Disease


Sponsor

Stichting International Registry for Alzheimer's Disease and other Dementias Foundation

Enrollment

50,000 participants

Start Date

Mar 30, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this international observational study is to evaluate long-term disease outcomes and treatment safety in people with Alzheimer's disease (PwAD), by collecting real-world data from routine clinical practice across global clinical centers. The InRAD Registry Observational Study has several aims: * To collect medical information for many years from a large group of people with Alzheimer's disease. This will be used for research, which will support improved understanding about the disease. * To enable researchers to look at the effectiveness, usefulness and safety of treatments for Alzheimer's disease. * To enable researchers to answer similar research questions and compare results in many different areas of the world. People with Alzheimer's disease who meet the eligibility criteria and agree to participate in the Study will be asked to visit their doctor (e.g. psychiatrist, geriatrician, or neurologist) at least once a year, or as frequently as is needed for their care. During or after their appointments they may be offered assessments, tests, medications, and treatments as determined by their doctor and their team. This is an observational data collection.


Eligibility

Inclusion Criteria4

  • Be undergoing diagnostic work-up for Alzheimer's disease (AD), OR
  • Have a confirmed diagnosis of AD (whether currently treated with an AD-specific treatment, or untreated),
  • Be attending an InRAD Center,
  • Have provided informed consent for long-term follow-up

Exclusion Criteria1

  • Any patient or legal representative who is unable or unwilling to provide a signed informed consent form

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Interventions

OTHERNone, this is a non-interventional observational study

None applicable


Locations(1)

UZLeuven

Leuven, Belgium

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NCT07213700


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