Initial Validation of the Vanderbilt ADHD Measure for Adolescent Patients in the ICISS Project

Background and Specific Aims:

Study Design: We will use the ICISS system's capacity for prospective and ongoing collection
of data from enrolled patients and their families to conduct our prospective, longitudinal
study consisting of a baseline assessment at enrollment into ICISS, a one-month re-test
assessment, and a follow-up assessment at either 3 months for patients who were
newly-diagnosed with ADHD or had a change in medication, or 6 months for patients with an
established diagnosis and no medication changes.

Recruitment and Consent: Once a patient has enrolled in ICISS, they will be asked if they
wish to participate in the modified Vanderbilt validation study, initially by phone call.
Some patients and/or their parents will want to discuss this in person or may not be reached
by phone call, in which case the research assistant will meet with them at the clinic visit.
This will take place in a quiet, confidential space.

However, with adolescents it is typical that the parent is not present at the clinic visit.
The Vanderbilt validation study will then be discussed with the parent verbally by phone and
consent will be implicit in answering the two Conners questionnaires when sent online.
Interested and eligible patients will be reminded in this email that participation in this
research study is completely voluntary, that a decision not to participate will not affect
their medical care in any way and that they may withdraw from the study at any time.

As participation in this study consists simply of answering two Conners questionnaires which
represent the standard of care for ADHD both nationally and in our clinics, presents
virtually no risk to the participant above the minimal risks associated with the general
ICISS study, and the parent, participant and teacher all have the option to simply not
respond to the email requesting Conners completion for this study.

Data Collection and Measures: The increase in effort to collect the additional data needed
for our study will be small as most of these measures are already being collected as part of
the larger ICISS implementation. The added time for each participant to complete the Conners
measures is marginal, on the order of 30 minutes total over a few interactions. After
enrollment into ICISS, all eligible patients aged 13-21 years will be asked to complete the
baseline youth self-report Vanderbilt-Long Form questionnaire and their parents the Parent
version. In addition, patients 13-18 years will have teachers complete the Teacher version.
All Long-Form versions include 18 items assessing the frequency (using a response scale of
0=Never, 1=Occasionally, 2=Often, 3=Very often) of symptoms and behaviors indicative of the
predominant subtype of ADHD (Inattentive, Hyperactive/Impulsive, or Combined). Additionally,
all three versions screen for Anxiety/Depression (7 items) and Oppositional-Defiant Disorder
(8 items), disorders that often co-occur with ADHD. Lastly, only the Parent and Teacher
versions include items assessing Conduct Disorder and School Performance (e.g., academic
performance, peer relations, classroom behavior, and assignment completion). To assess
test-retest reliability, we will again administer the Long-Forms at one-month follow-up.
However, for subsequent follow-ups (i.e., 3- or 6-months), we will administer the Short-Form
for all three Vanderbilt measures, which is the Long-Form but with the omission of
Anxiety/Depression and Oppositional-Defiant disorder items. We will also collect the
following data to address each of our study aims:

Aim 1: Feasibility and Acceptability: We will record patient, parent, and teacher response
and completion rates for each Vanderbilt administration. We will also measure the length of
time it takes for them to complete the Long Form (administered at baseline and one-month
follow-up) and Short Form (administered monthly thereafter), and provide comment fields so
that they can describe any difficulties they may have had in answering any of the questions.

Aim 2: Test-Retest and Inter-Rater Reliability: All patients, parents, and teachers will
again receive their respective Long-Form version of the Vanderbilt at one-month follow-up. As
part of the ICISS system, they will receive an email prompting them to complete the forms and
submit them electronically to ICISS where they will be made available to the team and the
patient's clinician. We will examine test-retest only for those patients who had no new
medications or changes in their medications and stable symptoms during the intervening month.
We will use the following two items to identify these patients: 1) "Since your/your child's
last medical appointment in the Adolescent Practice, have there been any changes in
your/his/her ADHD-related medications or therapies?" (Yes, No, I/My child do/does not receive
ADHD-related medications or therapies); and 2) "In general, how would you describe your/your
child's ADHD symptoms since your/his/her last medical appointment in the Adolescent
Practice?" (They have improved, They have stayed about the same, They have gotten worse). We
will only include patients for whom both the parent and patient reports indicate no changes
in symptoms or medications/therapies. We will examine both item-level retest agreement as
well as reliability of the overall screening outcome within each Vanderbilt domain (e.g.,
whether criteria are met for ADHD [and the predominant subtype], Oppositional-Defiant
Disorder, Anxiety/Depression, etc.).

We will also examine, when data are available, the level of "inter-rater" agreement, at the
domain level, across screening results obtained from youth, parent, and teacher forms.

Aim 3: Concurrent and Known-Groups Validity: For patients ages 13-18 years, we will
administer concurrent with the Vanderbilt at all assessment time points (see Study Design),
the Conners 3rd Edition Self Report Scale - Short Form (39 items); the Parent Rating Scale
(43 items); and the Teacher Rating Scale (39 items). For patients ages 19-21 yrs, we will
administer the Conners Adult ADHD Rating Scale Self-Report - Screening Version (30 items),
and ask parents to complete the corresponding Observer Report - Screening Version (30 items)
(Erhardt et al, 1999; Van Voorhees et al., 2011). We opted to use the adult ADHD rating
scales for patients aged 19 years or older since the Conners 3rd Edition measures have only
been validated up to age 18 years. We also opted to drop the teacher-based assessment for
patients older than 18 years due to concern that many teachers would be unable to assess
participants given minimal personal interaction in most college classes and the participant's
possible desire to keep ADHD diagnosis private. To test the ability of the Vanderbilt scores
to differentiate adolescents who are expected to differ (known-groups validity), we will
administer 1) a modified version of the Clinical Global Impression Scale [CGIS], a
single-item measure of adolescent global functioning (Busner & Targum, 2007) that parents and
youth both complete; 2) among patients 13-18 years, the PedsQL-Family Impact Module (Varni et
al., 2004) a 36-item parent-report measure of the impact a child's health condition is having
on parent/family quality of life; and among patients 19-21 years, the 29-item Adult ADHD
Quality of Life Questionnaire (AAQoL) (Matza et al., 2007). We will use these quality of life
and functioning measures to categorize youth into low, medium, and high symptom-severity
groups, and assess the ability of the Vanderbilt measures to discriminate these groups.
Finally, we will identify those patients who experience a change in their scores on the
validation measures (Conners, CGIS, PedsQL-Family Impact Module) over the follow-up period (3
months for newly-diagnosed or medication-change patients, 6 months for
established/no-medication-change patients) and assess the Vanderbilt's ability to detect that
change.

Inclusion Criteria:

- Patients ages 13-21 who already have an ADHD diagnosis or are being evaluated for
ADHD.

- Parent/guardian will be asked to participate for patients ages 13-21.

- Teachers will be asked to participate for patients ages 13-21.

- All informants should be able to read and understand English at a 5th grade reading
level; and enrolled in the ICISS system.

Exclusion Criteria:

- Cognitive impairment or developmental delay.