Survey to assess eligibility for neurology clinical trials
Official title: Triage Survey for Neurology Research Eligibility
Run by Adams Clinical · NCT06104852 · Data updated 2026-11-12
This study is trying to see if people with Alzheimer’s disease can join upcoming neurology clinical trials based on their health and medication use.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 600 (estimated) |
| Sponsor | Adams Clinical Research network |
| Locations | 3 sites (Boston, Massachusetts and 2 other locations) |
| Status | Recruiting |
| Started | June 2, 2023 |
| Main results expected | June 2, 2027 |
| Study ends | June 2, 2027 |
| Registry record updated | October 27, 2026 |
| Trial ID | NCT06104852 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 and older who are interested in participating in neurology clinical trials.
✕Probably not a fit
Patients who lack the cognitive ability to understand the screening process or have significant health issues that could impact safety or study results may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
TRIAGE-Neuro is an observational survey designed to evaluate potential participants' eligibility for industry-sponsored neurology clinical trials, specifically targeting individuals with Alzheimer Disease. The study aims to identify participant characteristics, the impact of prescribed memory medications on eligibility, and how changes in these medications affect cognitive assessment performance. Additionally, it will assess laboratory results that may exclude individuals from participation. This comprehensive approach will help streamline the recruitment process for future clinical trials in neurology.
Why it matters
Potential benefit: If successful, this study could enhance the recruitment process for neurology clinical trials, ultimately leading to more effective treatments for Alzheimer Disease.
How similar studies have gone: While this approach is somewhat novel in its focus on eligibility assessment through surveys, similar studies have shown success in improving participant recruitment in clinical trials.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participant and study partner (when applicable) have signed an ICF prior to study-specific procedures being performed. * Participant and study partner (when applicable) are at least 18 years old. Exclusion Criteria: * Participant lacks the language skills or cognitive ability to understand the screening process. * Participant is pregnant, breast-feeding, or planning to become pregnant. * History of a clinically significant illness which in the investigator's opinion may impact participant safety or the ability to analyze study results. * Participant represents an acute suicidal risk, as defined as a "yes" response to ideation on Columbia-Suicide Severity Rating Scale questions 4 or 5, or answer "yes" to behavior questions within 90 days of screening. * Moderate or severe substance use disorder within 90 days prior to screening, according to DSM-5 criteria that in the investigator's opinion could pose undue risk to the participant. * Any condition that in the investigator's opinion makes a participant unsuitable for the study. * Currently employed by Adams Clinical or a first-degree relative of an employee working on this study.
Where it's running
-
Adams Clinical
Watertown, Massachusetts, United States Recruiting -
Berman Clinical
New York, New York, United States Recruiting -
Copley Clinical
Boston, Massachusetts, United States Not yet recruiting
Study contacts
- Study coordinator: Sarah J Starling, PhD
- Email: sstarling@adamsclinical.com
- Phone: 6177448542
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.