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Moodbuster Autism

Effectiveness of a guided self-help, internet-delivered CBT-based intervention for improving depressive symptoms and wellbeing in autistic adults (Moodbuster Autism) - Moodbuster Autism

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58030
Enrollment
184
Registered
2025-04-16
Start date
2026-01-14
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Autism, Autism Spectrum Disorder (ASD), Autism Spectrum Condition (ASC), Neurodevelopmental Disorder, Neurodevelopmental Condition, Neurodivergence, Depression, Low mood, Depressive Symptoms

Interventions

“Moodbuster” is adapted to “Moodbuster Autism” through collaboration with autistic individuals. It is a guided online intervention based on CBT, aimed at improving mood in autistic adults. It consists

Sponsors

Vrije Universiteit
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a participant must meet all of the following criteria:A participant must have a formal clinical diagnosis of Autism Spectrum Disorder (ASD) as established by an authorized professional (e.g., psychiatrist/psychologist). This information is provided by the participant;  Be at least 18 years of age;Have a minimal score of 5 on the Patient Health Questionnaire-9 (PHQ-9);Possession of a computer (or laptop or tablet) with internet connectivity.

Exclusion criteria

Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study:High suicidal risk, as assessed in the online screening procedure (see 6.3) using the Mini International Neuropsychiatric Interview (M.I.N.I.) questionnaire. High risk is defined as answering ‘Yes’ to either question 4 (suicide plans) or 5 (suicide attempt), or to both questions 3 (suicidal thoughts) and 6 (lifetime suicide attempt) of the instrument. Initiation of antidepressant medication less than three months before the screening for this study;PHQ-9 score = 20 at screening (indicative of severe depressive symptoms);A reported DSM-V diagnosis of depression in the annual Netherlands Autism Register (NAR) survey;Currently undergoing psychological treatment for depression.Other co-occurring psychological disorders or conditions and somatic diseases are allowed, since rates of co-occurring psychiatric conditions and disorders are very high in this population. There is large heterogeneity in the prevalence rates of co-occurring mental conditions across development reported in studies (55), but estimates range from 28 - 81% (4, 56). Anti-depressant and other care usage will be monitored at all timepoints in both conditions.

Design outcomes

Primary

MeasureTime frame
Depression symptom severity (primary outcome)

Secondary

MeasureTime frame
Secondary outcomes: insomnia severity, anxiety, quality of life, daily functioning. Outcomes will be measured at baseline, post-intervention (6 weeks after baseline), and 6 months follow-up. We will also explore moderators (e.g. baseline symptom severity, age, sex, and therapeutic alliance) of the intervention effect and predictors of treatment outcome to determine who benefits most of the intervention. 

Countries

Netherlands

Contacts

Public ContactK.L. Spaargaren

Vrije Universiteit

k.l.spaargaren@vu.nl+31205989698

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 3, 2026