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Internet Videoconferencing-Delivered Cognitive Behavioural Therapy for Adult Attention-Deficit/Hyperactivity Disorder: A Feasibility Study

Internet Videoconferencing-Delivered Cognitive Behavioural Therapy for Adult Attention-Deficit/Hyperactivity Disorder: A Feasibility Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001200471
Enrollment
8
Registered
2025-10-31
Start date
2026-02-10
Completion date
2026-10-12
Last updated
2026-06-08

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

Conditions

None listed

Brief summary

The purpose of this study is to examine the efficacy, feasibility, and acceptability of videoconferencing-delivered cognitive behaviour therapy (CBT) for Adult Attention-Deficit/Hyperactivity Disorder (ADHD) in adults. After assessment, all participants will complete 10 sessions of vCBT with a psychologist.

Interventions

Treatment consists of individually delivered internet-videoconferencing delivered CBT (vCBT; 10x weekly 50-minute sessions). The vCBT will be manualised and will cover: psychoeducation about ADHD and goal setting; organisational skills; reducing distractibility; psychoeducation on the CBT model of ADHD; cognitive restructuring to develop adaptive thinking; and relapse prevention. The vCBT treatment will be provided by a provisional psychologist or psychologist with 1-5 years of experience. Adher

Treatment consists of individually delivered internet-videoconferencing delivered CBT (vCBT; 10x weekly 50-minute sessions). The vCBT will be manualised and will cover: psychoeducation about ADHD and goal setting; organisational skills; reducing distractibility; psychoeducation on the CBT model of ADHD; cognitive restructuring to develop adaptive thinking; and relapse prevention. The vCBT treatment will be provided by a provisional psychologist or psychologist with 1-5 years of experience. Adherence to the treatment will be monitored by the clinician each week.

Sponsors

University of Technology Sydney
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1) Presently residing in Australia; 2) Aged 18 years or over; 3) Fluent in English; 4) Meets criteria for ADHD and the disorder is of at least “moderate severity” (defined as a score of 4 on the DIAMOND module severity measure); 5) Medication-free or on a stable dose (6 weeks) of psychotropic medication or stimulant medication; and 6) Not presently receiving regular psychological services for their ADHD-related challenges (defined as sessions at least once a week with a qualified mental health professional, including an ADHD coach); and 7) Have access to a private location to complete the treatment for the duration of the study.

Exclusion criteria

1) Suicide risk as assessed by item 9 of the Patient Health Questionnaire-9 item (PHQ-9; a score of 2 or above) at baseline, or the Colombia Suicide Severity Rating Scale (C-SSRS), or a response of ‘yes’ to item 1–3 of the risk questionnaire, or via clinician judgement during the diagnostic interview; 2) Engagement in non-suicidal self-injury in the past 12 months; 3) Daily use of alcohol or illicit drugs (meaning illegal drugs, pharmaceutical drugs used outside their prescribed or intended use, and other substances inappropriately used); 4) The presence of a schizophrenia spectrum disorder, bipolar disorder, substance use disorder, or anorexia nervosa as assessed by the DIAMOND semi-structured clinical interview; 5) Any significant cognitive/intellectual impairment as assessed during the diagnostic interview; 6) A medical condition that may interfere with treatment; 7) No access to a computer with a camera and stable internet on a regular basis; 8) Is not willing to engage in treatment on a regular basis using internet-videoconferencing software; or 9) Does not meet the threshold on the Adult ADHD Self-Report Screening Scale for DSM-5 (ASRS-5) and the WURS-25 (Wender Utah Rating Scale-25).

Outcome results

None listed

Source: ANZCTR · Data processed: Jun 11, 2026