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A pilot randomised controlled trial of an internet-based cognitive behavioral therapy (CBT) treatment for adolescent anxiety

A pilot randomised controlled trial of an internet-based cognitive behavioral therapy (CBT) treatment for adolescent anxiety

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN79652741
Enrollment
60
Registered
2012-06-11
Start date
2012-06-01
Completion date
Unknown
Last updated
2018-07-30

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

Conditions

Topic: Mental Health Research Network

Interventions

Adolescents will be randomised to receive either internet-based CBT (n=20), the same internet-based CBT with additional parental sessions (n=20), or waitlist control (n=20) 1. CBT for adolescent anxi

Sponsors

University of Reading (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Current primary anxiety disorder identified as primary problem 2. Any psychoactive medication at a stable dose for at least two months before the initial assessment, with agreement to maintain that dose until after the laboratory assessment 3. Able to understand and speak English at an age-appropriate level 4. Parent who is primary caregiver and the person that the adolescent lives with (for the majority of the time) agrees to participate in the study 5. Target Gender: Male & Female; Upper Age Limit 18 years; Lower Age Limit 13 years

Exclusion criteria

Exclusion criteria: 1. Presence of psychotic symptoms, substance dependence, a risk of deliberate self-harm, attention deficit hyperactivity disorder (ADHD), conduct disorder, an autistic spectrum disorder or learning problems that would interfere with their understanding and participation in the trial (based on school/clinic/parent information) 2. Currently receiving therapy for their anxiety disorder 3. Parent has a significant intellectual impairment (as evidenced by them receiving a service from the local learning disabilities service) Non-anxious adolescents: Parent has a significant intellectual impairment (as evidenced by them receiving a service from the local learning disabilities service)

Design outcomes

Primary

MeasureTime frame
Clinical diagnoses; Timepoint(s): post-treatment and at 6-month and one-year follow-up

Secondary

MeasureTime frame
Added 12/04/2016: 1. Anxiety severity, measured by the ADIS-C/P 2. Self-report measure of anxiety symptoms (SCAS-C/P) 3. Impact of anxiety on the adolescent's life (CAIS-C/P) Timepoint(s): post-treatment and at 6-month and one-year follow-up

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026