A Study Of Evaluating Large Language Model Coding For DPICS
Overview
Tab Title Description
Study type
ObservationalDescribes the nature of a clinical study. Types include:
- Observational study — observes people and measures outcomes without affecting results.
- Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
- Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
Study IDs
Site IRB
- Rochester, Minnesota: 26-009092
About this study
The purpose of this study is to derive DPICs coding from LLMs using voice recordings from patent-child interactions at home.
Participation eligibility
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria for Children:
Ages 3-7 at time of enrolment
Outpatients
Any gender, race, or ethnicity
Able to provide developmentally appropriate informed assent, and parents or legal guardians able to provide informed consent
EBP Severity rated above the clinically significant range (≥120; T-score ≥ 60) (Eyberg Child Behavior Inventory- ECBI; Eyberg & Pincus, 1999).
Need for more intensive behavioural treatments such as ER visit for behavioral dyscontrol or hospitalization will not be exclusionary or exit criteria.
To be able to speak and understand English
Children included in the study will be allowed to use psychotropic medications (such as stimulants for ADHD) during the trial monitored by their clinician (combined treatment).
Exclusion Criteria Children:
Formal diagnosis of Severe Intellectual disability, Severe Autistic Spectrum Disorder, or a psychotic disorder for the child
Parents not consenting to study
Parents or child is not able to adhere to the study protocol. This is based on the principal investigator’s discretion
Unable to speak and understand English
Refusal or withdrawal of consent, inability, or unwillingness to adhere to study procedures
Any unstable medical condition
Inclusion Criteria Adults (Parents or legal caregiver):
Able to record the parent-child dyadic interaction into mobile application for 5 minutes while practicing the PCIT lessons.
Ages 18-99
Any gender, race, ethnicity
Able to provide informed consent
To be able to speak and understand English
Exclusion Criteria Adults (Parents or legal caregiver):
Unable to speak and understand English.
Refusal or withdrawal of consent, inability, or unwillingness to adhere to study procedures
Any unstable medical/psychiatric condition
Note: Other protocol defined Inclusion/Exclusion Criteria may apply.
Eligibility last updated 008/03/2026. Questions regarding updates should be directed to the study team contact.
Participating Mayo Clinic locations
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
| Mayo Clinic Location |
Status |
|
Rochester, Minn.
Mayo Clinic principal investigator Magdalena Romanowicz, M.D. |
Contact us for the latest status |
|
More information
Publications
Publications are currently not available