Evidence map›Paper›PMID 41713568›Full record

Trial reportAcademic pediatrics2026

Personalized ADHD Medication Experiments to Inform Decisions About Continued Medication Use: An Open-Label Trial.

Alyssa K Banister, Jeffery N Epstein, Kevin A Hommel, Maggie Breslin, Melinda C MacDougall, Shelley Ehrlich, William B Brinkman

Abstract readClinical Trial
In one paragraph

Trial report in Academic pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Alyssa K BanisterDivision of General & Community Pediatrics (AK Banister, MC MacDougall, and WB Brinkman), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio. Electronic address: alyssa.banister@cchmc.org.
Jeffery N EpsteinDepartment of Pediatrics (JN Epstein, KA Hommel, S Ehrlich, and WB Brinkman), University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Behavioral Medicine & Clinical Psychology (JN Epstein and KA Hommel), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Kevin A HommelDepartment of Pediatrics (JN Epstein, KA Hommel, S Ehrlich, and WB Brinkman), University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Behavioral Medicine & Clinical Psychology (JN Epstein and KA Hommel), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Maggie BreslinSchool of Visual Arts (M Breslin), New York, NY.
Melinda C MacDougallDivision of General & Community Pediatrics (AK Banister, MC MacDougall, and WB Brinkman), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Shelley EhrlichDepartment of Pediatrics (JN Epstein, KA Hommel, S Ehrlich, and WB Brinkman), University of Cincinnati College of Medicine, Cincinnati, Ohio; Department of Environmental and Public Health Sciences (S Ehrlich), University of Cincinnati College of Medicine, Cincinnati, Ohio; Division of Biostatistics and Epidemiology (S Ehrlich), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
William B BrinkmanDivision of General & Community Pediatrics (AK Banister, MC MacDougall, and WB Brinkman), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio; Department of Pediatrics (JN Epstein, KA Hommel, S Ehrlich, and WB Brinkman), University of Cincinnati College of Medicine, Cincinnati, Ohio.

Funding

Improving Medication Continuity among Adolescents with ADHDR34MH112648 · NIMH · CINCINNATI CHILDRENS HOSP MED CTR · PI BRINKMAN, WILLIAM BERNARD · 2018 to 2020
$716k
NIMH NIH HHS R34 MH112648
6 · The paper itself

Abstract

objectiveTo pilot test personalized stimulant medication experiments among children 11 to 15 years old with ADHD who questioned maintaining their current medication regimen.

methodsOpen-label trial involving 30 children (63.3% male, 86.7% white) and their parents. Experiments involved tracking personally meaningful measures daily for 2 weeks on their current regimen and 2 to 4 weeks after making a change. Validated outcome measures included the Decisional Conflict Scale (DCS) and the Decision-Making Involvement Scale (DMIS).

resultsParticipants selected 1 of 5 experiments: 1) try different dose or medication (50.0%); 2) start taking medicine on non-school days (20.0%); 3) stop taking medicine on non-school days (16.7%); 4) discontinue medicine (6.7%); and 5) no change (6.7%). Parents and children completed 92.8% (standard deviation [SD] = 7.5) of daily tracking questions. Following the experiment, 46.7% chose to continue the regimen tried during the experiment, 23.3% returned to their previous regimen, and 30.0% returned to their primary care provider to discuss other options. Participants felt less conflicted about treatment pre- to post-experiment, with parent mean (SD) pre DCS score = 15.9 (13.7)→post = 9.3 (10.0), P = .01; child pre DCS score = 26.3 (11.6)→post = 22.5 (13.1), P = .12. The mean (SD) DMIS subscale score for parents seeking information/opinions from their child increased from pre-to-post-experiment based on reports from children (pre = 2.6 (0.8), post = 2.9 (0.7), P = .03) but not parents (pre = 2.6 (0.7), post = 2.6 (0.7), P = .48). Most parents (83.3%) and children (76.7%) rated the medication experiment as helpful to extremely helpful.

conclusionsPersonalized medication experiments show promise to support the transition from family- to self-management of ADHD.

Indexed as

Attention Deficit Disorder with HyperactivityCentral Nervous System StimulantsDecision MakingMedication AdherencePrecision MedicineAdolescentChildFemaleHumansMaleParentsPilot ProjectsCentral Nervous System Stimulantsattention-deficit/hyperactivity disorderchild involvementdecision-makingpatient participation

Identifiers

PMID41713568
PMCPMC13078350

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.