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Does the Format of the Adult ADHD Self-Report Scale Impact the Results

U

University of Alberta

Status

Enrolling

Conditions

Attention Deficit Hyperactivity Disorder

Treatments

Other: Altered ASRS format, with shading and without grouping
Other: Altered ASRS format, without shading and with grouping
Other: Altered ASRS format, without shading and without grouping

Study type

Interventional

Funder types

Other

Identifiers

NCT06530758
Pro00144202

Details and patient eligibility

About

The World Health Organization Adult ADHD Self-Report Scale v1.1 (ASRS) is frequently used in family medicine clinics to screen for ADHD. Numerous studies have found the ASRS has a low positive predictive value. Compounding this concern is the format of the ASRS. Specifically, the answers on the ASRS that lead to screen positive results are shaded in gray and grouped together, which may make it easy for patients to discern which responses should be selected for a positive screen.

Full description

The ASRS is used widely to screen for ADHD in adults. It has 18 questions, with response options "never," "rarely," "sometimes," "often," and "very often." The 6 questions considered most predictive of ADHD are grouped together in Part A and questions that are meant to provide additional cues are grouped together in Part B. The options that are considered a positive response vary between questions; for some questions the option is at least "sometimes," while for others it is at least "often." The positive response options are shaded on the ASRS. A person is considered to have a positive screen if 4 of the 6 questions in Part A are positive.

The objective of this trial is to determine if the shading and grouping on the ASRS impacts screening results. This trial has a 2x2 factorial design set in a family medicine clinic(s). When a patients check in for an appointment, clinic staff will offer them a survey that includes 1) demographic questions and 2) 1 of the 4 versions of the ASRS, the version they receive is randomized (with programming). Most patients will take approximately 5 minutes to complete the survey prior to them seeing the family physician.

After 600 surveys are completed, we will provide the analytic data set to an outside biostatistician to determine if there is a significant interaction between the two factors (shading and grouping). If the interaction is significant we will continue recruiting participants.

Enrollment

600 estimated patients

Sex

All

Ages

19 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 19 - 65 years old
  • Patients who are registering for their appointment at the family medicine clinic
  • Patients who are expected to be in the reception area for ≥5 minutes before going to a clinic room

Exclusion criteria

  • Any patients who do not have the capacity to complete the form (e.g., cognitive impairment, unable to read English, unable to use a computer)

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

600 participants in 4 patient groups

ASRS without shading and with grouping
Experimental group
Description:
These participants will receive the ASRS form that does not have shading for the screen positive response options and has the questions grouped (ie, the headings "Part A" and "Part B" will remain on the form).
Treatment:
Other: Altered ASRS format, without shading and with grouping
ASRS with shading and without grouping
Experimental group
Description:
These participants will receive the ASRS form that has the screen positive response options shaded and has the questions ungrouped (ie, the headings "Part A" and "Part B" are removed).
Treatment:
Other: Altered ASRS format, with shading and without grouping
ASRS without shading and without grouping
Experimental group
Description:
These participants will receive the ASRS form that does not have shading for the screen positive response options and has the questions ungrouped (ie, the headings "Part A" and "Part B" are removed).
Treatment:
Other: Altered ASRS format, without shading and without grouping
Standard ASRS: with shading and with grouping
No Intervention group
Description:
These participants will receive the standard ASRS form. This form has the positive response options for each question shaded and has the questions grouped (ie, the headings "Part A" and "Part B" will remain on the form).

Trial contacts and locations

1

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Central trial contact

Roni Kraut

Data sourced from clinicaltrials.gov

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