The NICHQ Vanderbilt Assessment Scales are parent- and teacher-completed ADHD rating scales published by NICHQ with the American Academy of Pediatrics in 2002, with initial and follow-up forms and a third edition in 2019. Pediatric and primary care clinicians use them to gather cross-setting symptom, impairment, and follow-up data. They support a diagnosis; they never make one. This page covers how to document Vanderbilt results, with a fictional sample note.
Parents or caregivers and teachers complete the forms; the clinician scores and interprets; no qualification level, but the third-edition toolkit is licensed by the AAP
Pediatric and family-medicine clinicians, child psychiatry and psychology, school teams and 504 or IEP coordinators, payers and quality reviewers
4 to 10 chart lines per informant set · each form takes an informant about 10 minutes
Informant-rated ADHD scale (18 DSM-aligned symptom items scored 0 to 3, performance items scored 1 to 5, associated-condition screens; parent and teacher, initial and follow-up)
Pediatric ADHD evaluation (validated at ages 6 to 12), cross-setting collateral, associated-condition screening, medication titration and side-effect follow-up
First edition (2002) free from NICHQ with attribution; third-edition toolkit (2019) licensed by the AAP and EHR integration needs an institutional license; no authority mandates it
The NICHQ Vanderbilt Assessment Scales are informant-completed ADHD rating scales: a parent initial form, a teacher initial form, and parent and teacher follow-up forms that add a medication side-effect section. NICHQ published the first edition with the American Academy of Pediatrics in 2002, adapted from the Vanderbilt rating scales developed by Mark Wolraich and colleagues, so the accurate attribution is NICHQ and the AAP, not Vanderbilt University. A second edition followed in 2011 and the AAP's third-edition toolkit in 2019 (scoring instructions copyright 2020, DSM-5 aligned), with a fourth edition in development and no release date as of August 2026. Each form rates the 18 DSM-aligned ADHD symptom behaviors on a four-level frequency scale scored 0 to 3, rates performance in academic and social domains on a five-level scale, and screens for associated conditions (oppositional, conduct, and anxiety or depression symptoms on the parent form; a combined oppositional-conduct section, an anxiety or depression section, and an academic-performance flag on the teacher form).
Two facts govern the documentation. First, the Vanderbilt's own scoring is a two-part rule, not a total: an ADHD domain is scoring-positive when at least six of the nine behaviors in that domain are rated 2 or 3 and the performance-impairment criterion is met, which on the current edition means at least two performance ratings of 4 or one of 5 (the 2002 edition accepted any single 4 or 5). A symptom count without impairment is not a positive Vanderbilt result, and there is no official grand-total cutoff that establishes ADHD, even though raw sums and follow-up means exist. Second, the scale supports the diagnosis and never makes it: the AAP guideline requires DSM-5 criteria with symptoms and impairment in more than one major setting, established through parent, teacher or other school-personnel, and clinician information, and the community validation studies put the parent scale's positive predictive value at .19 and the teacher scale's at .32 against negative predictive values of .98 and .96, so a negative form excludes well and a positive form is a signal to evaluate. The full workup belongs in an ADHD evaluation report; the norm-referenced Conners 4 is the licensed comparator, and the ASRS and CAARS 2 take over at the adult boundary.
Pediatric and family-medicine practices are the core users, because the AAP's 2019 guideline expects a clinician to gather symptom and impairment information from more than one major setting before diagnosing ADHD and the Vanderbilt was built for exactly that collateral workflow: parent and teacher forms at evaluation, associated-condition screens alongside, and the follow-up forms for titration and side-effect monitoring once treatment starts. School teams see the results in school collateral notes and in the input that feeds a Section 504 statement or IEP input, where the form is one source among several and never the eligibility decision. In Canada, CADDRA's child pathway defaults to SNAP-IV parent and teacher forms with the Vanderbilt named as an acceptable substitute; in Australia the AADPA guideline (updated January 2026) lists it among example child instruments while insisting no diagnosis rests on scales alone. Direct validation is at ages 6 to 12; the AAP permits DSM-anchored use in preschoolers and adolescents without norms, and no Vanderbilt-specific preschool or adolescent diagnostic-accuracy study had been published as of August 2026, so those charts say so. Adult screening moves to the ASRS, and any diagnostic conclusion moves to the ADHD evaluation report.
No US, Canadian, or Australian authority prescribes a Vanderbilt note format, and none makes a score diagnostic. What survives review is a record that names the edition and form, the informant and setting for each form, both symptom-domain counts, whether the edition-specific impairment criterion was met, each associated-condition screen as a screen, an honest cross-setting synthesis, and, on follow-up, means against baseline with function and side effects. Each element below carries the pitfall that most often undermines it.
Edition and form. Name the edition or exact source (2002 first edition, 2011 second, 2019 third-edition toolkit) and whether each form is initial or follow-up. The editions differ in the impairment threshold, the length of the parent conduct section (14 versus 15 behaviors), and the follow-up arithmetic, so a reviewer cannot reproduce "Vanderbilt positive" without the edition. Pitfall: The 2002 impairment rule (any single performance rating of 4 or 5) applied to a current form, which manufactures false positives, or an indexed second-edition copy mistaken for the third because both use the two-4s-or-one-5 rule.
Informant, setting, date, and medication status. For each form, record who completed it (relationship; teacher role, subject, and how long they have observed the child), the completion date, and whether the child was unmedicated or on a named dose during the observation period, and when the rater usually sees the child relative to dosing. Pitfall: "Parent and teacher forms positive" with no dates, no observation window, and no medication context, which makes concordance meaningless and follow-up uninterpretable.
Domain counts, not a total. Chart inattentive x/9 and hyperactive-impulsive x/9 for each informant, counting behaviors rated 2 or 3 as symptom-positive; six or more of nine is the domain threshold, and both domains together is the combined pattern. Raw sums and means exist for research and follow-up, but no official grand-total cutoff establishes ADHD. Pitfall: "Total 42, diagnostic of ADHD," or one combined count that hides which domain carried it.
The performance-impairment rule. Record the number of performance ratings of 4 and 5 and whether the edition-specific criterion was met (current edition: at least two 4s or one 5). A domain is scoring-positive only when the symptom count and the impairment criterion are both met; you may separately document impairment established by interview, but do not alter the instrument classification. Pitfall: Performance items treated as optional, a symptom count called "positive" without impairment, or a rating of 3 read as impairment (on the current scale, 4 and 5 mark a problem).
Associated-condition screens as screens. Chart each screen with its numerator and denominator against the edition's threshold (for example, oppositional 4 of 8 on the parent form) plus the impairment finding, and write "screen positive" or "screen negative." The teacher form has one combined oppositional-conduct section and an academic-performance flag that points to records and achievement testing, not a diagnosis. Pitfall: "Vanderbilt diagnosed depression" or "conduct disorder per Vanderbilt": the 2012 validation found the parent comorbidity cutoffs had limited rule-in utility, and the oppositional cutoff was useful mainly for ruling out.
Concordance and discordance, without averaging. State which domains and impairments each informant reports and whether they agree, then interpret disagreement as information about settings, observation opportunity, structure, medication timing, learning demands, or family stress. When a teacher form is missing, document the attempts, the alternate school source used (another teacher, counselor, records, behavior plans), and whether the more-than-one-setting criterion is established, uncertain, or not met. Pitfall: Parent and teacher counts averaged into an artificial child, one rater dismissed as unreliable, or a diagnosis finalized on a parent form alone with no second-setting evidence.
Follow-up: means, function, side effects. On the current follow-up forms, calculate the mean rating for the nine inattentive and nine hyperactive-impulsive behaviors separately and compare each with its own baseline mean; record performance change and the side-effect section, with the medication, dose, dosing time, and observation interval, and the resulting decision. Pitfall: Follow-up scored by counting positives, baseline and follow-up on different informants or conditions, or side effects charted nowhere while the dose goes up.
VANDERBILT DOCUMENTATION BLOCK Date: [ ] Setting: [ ] Clinician: [ ] Child age: [ ] Edition / source: [2002 first / 2011 second / 2019 third-edition toolkit] Form A: [parent initial / follow-up] Informant: [ ] Completed: [date] Medication status during observation: [none / drug + dose + timing] Inattentive [ ]/9 Hyperactive-impulsive [ ]/9 (rated 2 or 3 = positive; 6+ of 9 = domain threshold) Performance: ratings of 4 [ ] of 5 [ ] -> impairment criterion [met / not met] (current edition: two 4s or one 5) Screens: oppositional [ ]/8 conduct [ ]/15 anxiety-depression [ ]/7 -> [screen positive / negative], not diagnoses Form B: [teacher initial / follow-up] Informant + role + observation period: [ ] Completed: [date] Medication status: [ ] Inattentive [ ]/9 Hyperactive-impulsive [ ]/9 Performance: [ ] Combined oppositional-conduct [ ]/10 anxiety-depression [ ]/7 Academic-performance flag: [ ] Cross-setting synthesis: [concordant / discordant: pattern by setting; missing form: attempts + alternate school source; more-than-one- setting criterion established / uncertain / not met] Interpretation: [Vanderbilt supports, does not establish, the diagnosis; integrated with history, onset, duration, differential, records] Follow-up (if applicable): baseline means I [ ] HI [ ] -> current I [ ] HI [ ]; performance change; side effects; drug/dose/timing; decision Plan: [evaluation steps / school supports / treatment / next forms + date] Clinician signature / credentials: Date:
Free to use and share, no signup. The PDF includes a one-page cheat sheet with element-by-element pitfalls and a pre-sign checklist; the DOCX is the blank documentation block, ready to adapt. Neither reproduces the scale items, forms, or scoring sheets.
Scenario: concordant parent and teacher third-edition initial forms reviewed at the second visit of a pediatric ADHD evaluation, with impairment met in both settings, negative associated-condition screens, and the diagnosis made on the full evaluation rather than the forms. All details are fictional.
Patient: D.K., 8 · Setting: Pediatric primary care, ADHD evaluation visit 2 · Clinician: A. Mehta, MD · Note date: 08/13/2026
Forms reviewed: NICHQ Vanderbilt initial scales, AAP toolkit third edition, no ADHD medication during either observation period. Parent initial form completed by mother 08/05/2026: inattentive 7/9, hyperactive-impulsive 6/9; performance ratings include three 4s and no 5s, impairment criterion met. Associated-condition screens: oppositional 2/8, conduct 0/15, anxiety-depression 1/7, all screen negative. Teacher initial form completed 06/2026 by the third-grade homeroom teacher over the final term of last school year (about nine months of daily observation), returned through the school office 08/07/2026: inattentive 8/9, hyperactive-impulsive 7/9; performance ratings include one 5 and one 4, impairment criterion met; combined oppositional-conduct 1/10, anxiety-depression 0/7, academic-performance flag not raised.
Synthesis: Parent and teacher reports are concordant for clinically significant inattentive and hyperactive-impulsive symptoms with impairment at home and school, meeting the current symptom-count and impairment rules for a combined-domain Vanderbilt result in both settings. Vanderbilt results support, but do not independently establish, the diagnosis. Integrated with the developmental and medical history from visit 1 (symptoms noted by kindergarten, persistent, in excess of developmental level), report cards and the second-grade behavior plan, today's interview, normal hearing and vision screens, no sleep-disorder symptoms, no learning-disorder signal on records or teacher flag, and negative anxiety and mood screens, findings meet criteria for ADHD, combined presentation. No better explanation identified.
Discussion and plan: Diagnosis, options, and expected course reviewed with the mother and D.K. in age-appropriate terms. Plan by shared decision: behavioral parent-training referral placed; letter to school requesting a Section 504 evaluation with the parent's consent, enclosing a summary (school eligibility is the school's determination); stimulant trial discussed with cardiovascular history reviewed and no contraindication, family to decide at a phone check-in within one week; if medication starts, parent and teacher follow-up forms in four weeks under the same informants and observation conditions, first prescriber follow-up within 30 days, side effects reviewed at each contact.
Administrative: Both forms scanned to the chart with completion dates and informant details; domain counts, impairment findings, and screen results entered in the structured ADHD flowsheet with the edition named. Two standardized informant instruments scored and interpreted this encounter, reported under 96127 per payer rules; no diagnosis coded from the forms alone.
This sample is fictional and for educational purposes. It does not describe a real patient or record; the scores, dates, and details are invented to show documentation structure and are not clinical guidance.
Writing these after every session? BastionGPT drafts complete notes from bullets, dictation, or a transcript.
Generate a note from bulletsUnited States: guideline convention, education law, and payer measures pull in different directions, and none names the Vanderbilt. The AAP's 2019 clinical practice guideline (CONVENTION) requires that DSM-5 criteria be met with documentation of symptoms and impairment in more than one major setting, drawing on parents or guardians, teachers, other school personnel, and involved mental health clinicians, and that alternative causes be ruled out; it requires a process to screen for associated conditions; and it does not name an instrument or require two positive forms, so "two informants" is shorthand for cross-setting evidence, which another credible school source can supply when a teacher form never returns. Under IDEA, 34 CFR 300.304 (LAW) requires a variety of assessment tools and forbids a single measure as the sole criterion for eligibility, and Section 504 evaluation duties (LAW, with 2016 federal guidance) turn on suspected disability and functional limitation, not on crossing a Vanderbilt cutoff, so a medical diagnosis and a positive form together do not produce an IEP or 504 plan; the school team decides on multiple sources. Stimulant prescribing carries state controlled-substance and PDMP obligations (LAW, varying by state) that attach to the prescription, not to a score, and no PDMP rule reviewed makes a Vanderbilt a prerequisite; defensible prescribing notes still carry the diagnostic basis, targets, cardiovascular and medical history, response, function, and adverse effects, which the follow-up forms document efficiently. AAP coding guidance maps an informant-completed Vanderbilt to 96127 rather than 96110 (CONVENTION), while units, bundling, and modifiers are PAYER POLICY. The HEDIS follow-up measure for children aged 6 to 12 newly prescribed ADHD medication (PAYER POLICY) counts a prescriber follow-up within 30 days of the first dispensing and, for the continuation phase, at least 210 treatment days with two additional follow-ups within 270 days after the initiation phase; it does not require a Vanderbilt result, so the record must support the dispensing chronology and the dated encounters, and the forms give those encounters their clinical content.
Canada and Australia name other defaults and stricter framing. CADDRA's current child flowchart (2025) places parent and teacher SNAP-IV forms, the CADDRA teacher assessment form, and a functional-impairment measure in its default workflow and expressly allows the Vanderbilt, Conners, or the Strengths and Difficulties Questionnaire instead (CONVENTION); its practice guidelines (4.1, 2021) call rating scales efficient but insufficient for diagnosis, because anxiety, depression, sleep apnea, anemia, and other conditions produce positive responses. Australia's AADPA guideline (2022, updated January 2026, NHMRC approval stated through 29 July 2027) says ADHD should not be diagnosed solely from rating scales or observation, requires information from more than one setting and reporter for children, and lists the Vanderbilt among example instruments (CONVENTION); the stimulant-authority layer is state law that names no scale and has been changing quickly through 2025 and 2026 (endorsed or authorized GP pathways in New South Wales, South Australia, Tasmania, the ACT, and Victoria; Queensland's post-December 2025 framework; monitored-medicines checks such as SafeScript, QScript, ScriptCheckWA, and Canberra Script), so an Australian note separates the clinical diagnostic basis from the authority, approval, and monitored-medicines requirements. On the evidence: the parent scale in a community sample (2013) showed sensitivity .80, specificity .75, positive predictive value .19, and negative predictive value .98, and the teacher scale .69, .84, .32, and .96, which is why the authors themselves read the numbers as an argument for multiple observers; a 2015 study of 6,659 children found parents rate higher than teachers, with weak agreement on inattention and stronger agreement on hyperactivity-impulsivity, so discordance is expected, not error; the 2022 nationally representative parent norms (1,570 caregivers, ages 5 to 12) were built on the older 55-entry form and did not create demographic cutoffs; a 2012 study found the parent comorbidity cutoffs had limited rule-in utility; and a 2024 AAP-AHRQ review of 231 studies found tools perform worse when separating ADHD from other referred conditions than from community controls. Direct validation is at ages 6 to 12: no Vanderbilt-specific preschool diagnostic-accuracy study was found, and the registered adolescent-modification study had no posted or published results as of August 2026.
Rights are more layered than "the Vanderbilt is free." NICHQ offers the 2002 first edition for download without charge and asks publications that use it to reference NICHQ; the PDF carries the 2002 AAP and NICHQ copyright and no license authorizing re-typesetting, modification, removal of notices, or unrestricted redistribution. The 2019 third-edition toolkit is sold and licensed by the AAP: its product page states that the single-user license does not support EHR integration and that an institutional license is required for multi-user access or EMR and EHR integration (live August 2026), AAP permissions require material to be reproduced exactly with changes needing written consent, Spanish forms ship in the toolkit, and no NICHQ or AAP source publishes a carve-out for a public website that reproduces the items and scores responses, whether or not it is free; a calculator that accepts already-derived counts without displaying item wording is lower-risk, not AAP-approved. The NICHQ Vanderbilt Assessment Scales are published by NICHQ with the American Academy of Pediatrics, and the third-edition toolkit is copyright American Academy of Pediatrics. BastionGPT is not affiliated with, or endorsed by, NICHQ, the American Academy of Pediatrics, or the scales' authors. This page reproduces no items, forms, or scoring sheets and describes the scoring architecture in original prose.
The numbers behind these errors are specific. In the community validation studies the parent scale's positive predictive value was .19 and the teacher scale's .32, against negative predictive values of .98 and .96; a study of 6,659 children found parent-teacher agreement weak for inattention; the 2002 first edition accepted any single performance rating of 4 or 5 as impairment while the current edition requires two 4s or one 5; and the AAP's third-edition license excludes EHR integration without an institutional license. The BastionGPT Clinical Advisory Board sees the same errors most often in Vanderbilt documentation reviews:
BastionGPT is specifically trained, tuned, and clinically tested on behavioral health progress notes and screening documentation.
See how clinicians use it day to day on the AI therapy notes page.
Many BastionGPT users report saving more than 90 minutes per day on documentation.
HIPAA-compliant with a signed BAA on every plan. Your data is never used to train models. BastionGPT drafts, you review and sign.
As a two-part rule per informant, not a total. On the initial forms, each of the 18 DSM-aligned ADHD behaviors is rated 0 to 3, a rating of 2 or 3 counts as symptom-positive, and six or more of the nine behaviors in a domain meets the inattentive or hyperactive-impulsive threshold, with both domains together giving the combined pattern. Separately, the performance items rate functioning on a five-level scale, and the impairment criterion on the current edition is at least two ratings of 4 or one rating of 5 (the 2002 first edition accepted any single 4 or 5). A domain is scoring-positive only when both parts are met; a symptom count without impairment is not a positive Vanderbilt result. The associated-condition sections have their own thresholds and are screens. Raw sums and means exist for research and follow-up, but no official grand-total cutoff establishes ADHD, so "total 42, diagnostic" is a made-up rule.
It matters. The 2002 first edition (free from NICHQ) used any single performance rating of 4 or 5 as impairment, a 14-behavior parent conduct section, and a single combined symptom sum on its follow-up forms. The 2011 second edition adopted the two-4s-or-one-5 impairment rule but kept the 14-behavior conduct section. The 2019 third-edition AAP toolkit (scoring instructions copyright 2020) is DSM-5 aligned, has a 15-behavior parent conduct screen, uses two 4s or one 5, and tracks follow-up as separate inattentive and hyperactive-impulsive means; a fourth edition is in development. Freely circulating PDFs on hospital and university sites are mostly first- and second-edition copies. Name the edition or exact source in the chart, and never apply the 2002 impairment rule to a current form; the impairment rule alone cannot tell you which edition you hold, because the second and third share it.
You need evidence of symptoms and impairment in more than one major setting; you do not need two positive Vanderbilt forms. The AAP guideline draws that evidence from parents or guardians, teachers, other school personnel, and involved mental health clinicians, and it names no instrument, so a missing teacher form does not automatically block a diagnosis when reliable school-setting information arrives another way (a second teacher, counselor, or school psychologist; report cards, behavior plans, disciplinary or psychoeducational records; direct school communication). Document the attempts and dates, the alternate source, and whether the more-than-one-setting criterion is established, uncertain, or not met. When only a parent form exists and no second-setting evidence does, chart a positive parent screen and a pending evaluation, not a completed diagnosis. Return rates are a structural problem: a 195-child study of parent-return agreements found teacher forms came back 71% of the time before and 76% after, no significant change.
Do not choose one by default and do not average them. Preserve each informant's counts and impairment findings, describe the setting-specific pattern, and treat the disagreement as information: parents rate higher than teachers on average, agreement is weak for inattention and stronger for hyperactivity-impulsivity across 6,659 children, and different observers validly see different contexts. Then investigate: classroom structure and size, academic level and homework conflict, sleep, anxiety, learning, family stress, medication timing if applicable, observation opportunity, another teacher or activity setting, and school records. If credible information shows impairment only at home, the more-than-one-setting criterion is not yet established; the home concern may still warrant intervention and differential assessment, and the chart says exactly that.
The 2002 first edition is free to download from NICHQ, which asks for a reference to NICHQ in publications and grants no license to re-typeset, modify, remove notices, or redistribute without limit; the PDF carries the 2002 AAP and NICHQ copyright. The 2019 third-edition toolkit is sold and licensed by the AAP, and its product page states that the single-user license does not support EHR integration and that an institutional license is required for multi-user access or EMR and EHR integration; AAP permissions require exact reproduction with written consent for changes, and Spanish forms are part of the licensed toolkit. No NICHQ or AAP source publishes a carve-out for a free public website that reproduces the items and scores responses, so a tool that displays item wording or rebuilds the form should obtain written permission; a calculator that only accepts already-derived counts is lower-risk, not approved. Terms as stated on the NICHQ and AAP pages in August 2026; confirm before building anything.
As a screen. Record the exact numerator and denominator against the edition's threshold (the parent form separates oppositional and conduct sections and has an anxiety-depression section; the teacher form has one combined oppositional-conduct section, an anxiety-depression section, and an academic-performance flag), the impairment finding, and the words "screen positive." Then document the targeted history, severity, duration, settings, a risk inquiry when clinically indicated, collateral, the differential, and the plan for assessment, treatment, or referral. The 2012 validation study found the parent comorbidity cutoffs generally lacked adequate utility for confirming or excluding structured-interview diagnoses, with the oppositional cutoff useful mainly for ruling out oppositional defiant disorder, which is why "Vanderbilt diagnosed depression" is wrong twice over. The teacher's academic flag points to records and achievement testing, not to a learning-disorder diagnosis.
With the follow-up forms, scored differently from intake. On the current edition, calculate the mean rating for the nine inattentive and the nine hyperactive-impulsive behaviors separately and compare each with its own baseline mean; record performance change (how many 4s and 5s remain), the side-effect section, the medication, dose, dosing time, and the rater's observation interval relative to dosing, and the decision (continue, adjust, change). Use the same informants under comparable conditions, and repeat when results can inform titration, after meaningful dose changes, and periodically in maintenance; no official source fixes an interval. HEDIS timing (a prescriber follow-up within 30 days of the first dispensing for children 6 to 12, then two more visits in the continuation phase) is an encounter requirement, not a form requirement, and PDMP checks attach to the prescription under state law. Charting side effects nowhere while the dose rises is the follow-up error reviewers see most.
Choose by age, question, and setting. The Vanderbilt suits pediatric primary care and school-collateral workflows at ages 6 to 12 when DSM-aligned domain counts, an impairment rule, associated-condition screens, and follow-up with side-effect tracking are what you need; it has no response-style index and its current edition is licensed, not simply free. The Conners 4 is a norm-referenced, licensed instrument for ages 6 to 18 with parent, teacher, and self-report forms, broader content, and response-style indicators, interpreted on its own norms and never on Vanderbilt thresholds. The SNAP-IV is the free scale CADDRA names as its default parent and teacher form in Canada. The ASRS and CAARS 2 are adult instruments, not pediatric substitutes. None of them is an evaluation: the diagnostic formulation belongs in the ADHD evaluation report, and a positive scale of any kind is a reason to do one.
Yes. Give it the facts (edition, each form's informant, completion date, and medication status, the domain counts and performance ratings, the screen results, the history and records, and the plan) and it drafts the full entry: counts and impairment per informant, screens as screens, the cross-setting synthesis, the supports-not-establishes statement, and the plan with dates and owners, ready for your review. It can also check a finished note for a form charted as the diagnosis, a count without the impairment rule, an unnamed edition, averaged informants or a missing form with no trail, and follow-up scored like an intake. BastionGPT is HIPAA-compliant with a signed BAA on every plan, and your data is never used to train models.
The instrument facts and compliance claims on this page trace to these sources, last verified August 2026:
Educational content, not legal or billing advice. Sample notes are fictional. Follow your organization's policies and your board, payer, and jurisdiction requirements.