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Triage Survey for Neurology Research Eligibility

NCT06104852 · Adams Clinical
In plain English

Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.

About this study
TRIAGE-Neuro is a survey study designed to assess potential participants' eligibility to screen for industry-sponsored neurology clinical trials. Secondary objectives include identifying participant characteristics among the clinical trial-seeking population, identifying the percentage of potential participants currently taking prescribed memory medications that could exclude them from clinical trial participation, examining how changes in prescription memory medications impact performance on cognitive assessments, and identifying the percentage of potential participants whose laboratory results could exclude them from clinical trial participation.
Eligibility 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.
Study design
Enrollment target: 600 participants
Age groups: adult, older_adult
Timeline
Starts: 2023-06-02
Estimated completion: 2027-06-02
Last updated: 2023-10-27
Interventions
Other: SurveyOther: Optional Medication Washout
Primary outcomes
  • Proportion of the clinical trial seeking population for whom industry-sponsored clinical research is clinically appropriate, as defined as those who go on to screen for a study. (Up to 52 weeks)
Sponsor
Adams Clinical · network
Contacts & investigators
ContactSarah J Starling, PhD · contact · sstarling@adamsclinical.com · 6177448542
All locations (3)
Copley ClinicalNot Yet Recruiting
Boston, Massachusetts, United States
Adams ClinicalRecruiting
Watertown, Massachusetts, United States
Berman ClinicalRecruiting
New York, New York, United States
Triage Survey for Neurology Research Eligibility · TrialPath