Assessment & Research

Preliminary study of imipramine in profoundly retarded residents.

Aman et al. (1986) · Journal of autism and developmental disorders 1986
★ The Verdict

Imipramine at 3 mg/kg/day made adults with profound ID more irritable, hyper, and less skilled—skip it.

✓ Read this if BCBAs serving adults with profound ID in residential or day programs.
✗ Skip if Clinicians working only with children or mild ID.

01Research in Context

01

What this study did

Researchers gave imipramine to adults with profound intellectual disability. They used a double-blind crossover design so no one knew who got the pill or the placebo.

Each adult got 3 mg of imipramine for every kilogram of body weight each day. The team watched for changes in mood, movement, and self-care skills.

02

What they found

The drug made things worse. Adults became more irritable, more withdrawn, and moved around too much.

Skills like feeding and dressing dropped. The study stopped early because the harm was clear.

03

How this fits with other research

Clarke et al. (1998) later tested SSRIs in the same group. About one in four adults also got worse on those newer antidepressants. Both papers warn that any antidepressant can backfire in people with severe ID.

Webb et al. (1999) hunted for RCT proof that antipsychotics help challenging behavior. They found almost none. Together with Osnes et al. (1986), the message is: pills for behavior in ID need rock-solid evidence before you try them.

Cohen-Almeida et al. (2000) showed atypical antipsychotics had milder side-effects than older ones. That finding does not clash with G et al.; it simply shifts the risk question to a different drug class.

04

Why it matters

If a psychiatrist suggests imipramine for your adult client with profound ID, show them this paper. The risk of sudden behavior collapse is real. Push for a functional assessment and evidence-based behavioral interventions first. When medication is on the table, ask for data from people who match your client’s profile, not just general psychiatry studies.

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Add a red-flag note in the behavior plan: ‘Imipramine worsened skills and mood in RCT—discuss alternatives before any tricyclic trial.’

02At a glance

Intervention
not applicable
Design
randomized controlled trial
Sample size
10
Population
intellectual disability
Finding
negative

03Original abstract

This was a double-blind, placebo-controlled crossover trial of imipramine (3 mg/kg/day) in 10 profoundly retarded residents. Two groups were formulated: one with depressivelike (or affective) symptoms and one with acting-out behaviors. Measures of drug response included ratings of ward behavior using the Aberrant Behavior Checklist, interval samples of behavior in the living units, and observations of behavior in a playroom situation. Results indicated that the drug caused behavioral deterioration in the Irritability, Lethargy/social withdrawal, and Hyperactivity dimensions of the rating scale, irrespective of subgroup. In addition, gross motor activity was significantly increased on the wards due to imipramine, and it was found that the affective group became less active and the acting-out group more active during free play. Physical side effects were uncommon. These unexpected adverse behavioral effects were discussed with respect to dosage and diagnostic considerations.

Journal of autism and developmental disorders, 1986 · doi:10.1007/BF01531659