Practitioner Development

Clinical Informed Consent and ABA

Graber et al. (2024) · Behavior Analysis in Practice 2024
★ The Verdict

Document the risk talk, not just the signature, or you risk losing in court.

✓ Read this if BCBAs writing treatment plans, supervisors, and clinic directors.
✗ Skip if RBTs who do not manage consent discussions.

01Research in Context

01

What this study did

Graber et al. (2024) read every major U.S. court case about informed consent. They picked the ones that shape what clinicians must tell clients before treatment starts.

The authors turned the legal rules into plain steps a BCBA can follow. They matched each step to the BACB Ethics Code so you know you are covered both legally and ethically.

02

What they found

Two landmark cases matter most: Canterbury v. Spence and Cobbs v. Grant. Courts say you must share the risks a reasonable person would want to know, not just what you think is important.

If a client can show you left out a risk, they can sue. The paper lists the exact words judges look for and the paper trail you need to stay safe.

03

How this fits with other research

Falakfarsa et al. (2022) found that only a large share of published ABA studies report treatment-integrity data. Graber’s legal review says poor documentation is exactly what loses lawsuits. Together, the papers flag the same gap: we are not writing enough down.

Castañe et al. (1993) showed that 30 years ago most child studies skipped integrity checks. Graber updates the stakes: today, missing data can break both ethics and the law.

Plattner et al. (2023) report that BCBAs feel under-trained in soft skills. Graber adds a new must-have skill: knowing consent case law. Both papers call for stronger supervision targets.

04

Why it matters

You already get consent signed, but this review says that is not enough. You need to document what you said about risks, benefits, and alternatives. Add a short note in the file: "Discussed possible escape extinction crying, parent stated understanding." Do it every time and you meet both the Ethics Code and the courts.

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Add a one-line consent note template to your session note and fill it every session.

02At a glance

Intervention
not applicable
Design
narrative review
Finding
not reported

03Original abstract

The practice of clinical informed consent in America is governed by over 100 years of case law. Although predominant ethics resources for behavior analysts offer some guidance regarding the provision of clinical informed consent, such guidance remains limited. The goal of this article is thus to expand the contemporary literature on clinical informed consent in behavior analysis by providing a historical and contemporary guide to relevant case law. The article will highlight seminal moments in the history of case law regarding clinical informed consent, discuss their applicability to the process of clinical informed consent in behavior analysis, and provide an enhanced understanding of the ethical and legal obligations related to informed consent in the therapeutic context. The online version contains supplementary material available at 10.1007/s40617-023-00902-0.

Behavior Analysis in Practice, 2024 · doi:10.1007/s40617-023-00902-0