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Behavioral Activation for Treatment of Depression in Autistic Adolescents With Below Average Intelligence

Behavioral Activation for Treatment of Depression in Autistic Adolescents With Below Average Intelligence

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07812870
Enrollment
18
Registered
2026-09-10
Start date
2026-08-10
Completion date
2027-09-01
Last updated
2026-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism, Depressed, Depressed Mood

Keywords

Autism, Depression

Brief summary

Autism spectrum disorder is characterized by differences in social communication/interaction and the presence of restricted/repetitive behaviors, with significant heterogeneity in terms of autistic features, language ability, and cognitive characteristics. About 2-3% of individuals in the United States are autistic, and most autistic individuals have co-occurring mental health conditions. Autistic people are 3-4 times more likely to experience depression than non-autistic people. Of the emerging depression treatment research with autistic people, none to date has focused on developing and testing a depression treatment for autistic youth with below average cognitive abilities - a group which comprises over 50% of the autistic community. Therefore, this study seeks to evaluate the feasibility (Aim 1), acceptability (Aim 2), and preliminary treatment effects (Aim 3) of an extension of Behavioral Activation for Depression in Autistic Adolescents (BA-A), adapted to meet the needs of cognitively lower functioning autistic youth.

Interventions

BEHAVIORALBA-A

BA-A is an individually delivered manualized 12-session treatment that utilizes established behavioral strategies and incorporates common mental health treatment adaptations for autistic young people.

Sponsors

Stony Brook University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* 12-17 years old * Autism diagnosis * Symptoms of depression (more specifically, Children's Depression Inventory, Second Edition parent-report and/or self-report T-score ⩾ 65) * IQ 60-84 * Stable on medications for mood, anxiety, and/or behavior for 3 months * Participation of same parent(s) in all therapy sessions and assessment visits

Exclusion criteria

* Participation in another psychotherapy during the study period * Imminent risk of harm to self and/or others * Bipolar disorder, a personality disorder, and/or schizophrenia or another psychotic disorder

Design outcomes

Primary

MeasureTime frame
Children's Depression Rating Scale, RevisedBaseline, Post-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline]), 1-Month Follow-Up (1 month following completion of therapy sessions)
Children's Depression Inventory, Second EditionBaseline, Post-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline]), 1-Month Follow-Up (1 month following completion of therapy sessions)
Aberrant Behavior ChecklistBaseline, Post-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline]), 1-Month Follow-Up (1 month following completion of therapy sessions)
Behavioral Activation for Depression Scale-Short FormBaseline, Post-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline]), 1-Month Follow-Up (1 month following completion of therapy sessions)
Acceptability of Intervention MeasurePost-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline])
Intervention Appropriateness MeasurePost-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline])
Feasibility of Intervention MeasurePost-Treatment (i.e., after completion of 12 weekly therapy sessions [typically 12-13 weeks after baseline])

Countries

United States

Contacts

CONTACTMichelle Menezes, PhD
autismandneurodiversitylab@gmail.com631-638-3819
PRINCIPAL_INVESTIGATORMichelle Menezes, PhD

Stony Brook University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 11, 2026