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临床试验/NCT06530758
NCT06530758已完成不适用

Does the Format of the Adult ADHD Self-Report Scale Impact the Results: a Randomized Controlled Trial

University of Alberta1 个研究点 分布在 1 个国家目标入组 587 人开始时间: 2024年7月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
587
试验地点
1
主要终点
Screen positive rate

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Screening
盲法
None

入排标准

年龄范围
19 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •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)

研究组 & 干预措施

ASRS without shading and with grouping

Experimental

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).

干预措施: Altered ASRS format, without shading and with grouping (Other)

ASRS with shading and without grouping

Experimental

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).

干预措施: Altered ASRS format, with shading and without grouping (Other)

ASRS without shading and without grouping

Experimental

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).

干预措施: Altered ASRS format, without shading and without grouping (Other)

Standard ASRS: with shading and with grouping

No Intervention

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).

结局指标

主要结局

Screen positive rate

时间窗: Through study completion, estimated to be 2 months

Poisson regression to determine the relative risk of a screen positive among the different versions of the form. We will include the following covariates: shading, grouping, shading x grouping, suspect ADHD without diagnosis, ADHD diagnosis, sex, and age.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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