Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06661460 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Internet-Delivered Cognitive Behavioral Intervention for Youths With Anxiety Disorders

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Trial status: Not Yet Recruiting to Recruitingv4 Show 4 more changesShow less
    • Primary completion date: Jan 1, 2027 to Mar 1, 2027
    • Study completion date: Apr 1, 2027 to Jun 1, 2027
    • Start date changed from estimate of Oct 1, 2025 to Dec 12, 2025
    • Site details revised
  2. Notable Primary completion date: Jul 1, 2026 to Jan 1, 2027
    • Start date: Apr 1, 2025 to Oct 1, 2025
    • Study completion date: Oct 1, 2026 to Apr 1, 2027
    v3
  3. Minor Secondary endpoints: 32 to 31v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
3,263 trials monitored
See 159 trials at risk
The goal of this study is to develop a new internet-delivered cognitive behavioral therapy (ICBT) intervention for youths with anxiety disorders based on the best current knowledge about effective cognitive behavioral therapy for the target group, refine the intervention in collaboration with patient and public representatives, and conduct a preliminary evaluation of the treatment effects in an open clinical trial. The primary objective of the study is: 1\. To evaluate the preliminary efficacy of a newly developed ICBT intervention for children and adolescents with anxiety disorders in reducing anxiety severity, as measured by the Pediatric Anxiety Rating Scale (PARS). Secondary objectives of the study are: 1. To examine the preliminary efficacy (PARS) of the ICBT intervention at 3 months post-treatment. 2. To examine how youths with anxiety disorders, their caregivers, therapists, and healthcare leadership experience the ICBT intervention. 3. To examine factors (e.g., age, type of anxiety disorder, presence of depressive symptoms, experiences of ICBT) that predict treatment outcome. 4. To examine how the ICBT intervention can be improved (e.g., treatment content and technical delivery) for future use. Participants will: * Undergo ICBT treatment for anxiety disorders during 12 weeks * Complete questionnaires at multiple time points throughout the study * Participate in follow-ups post-treatment and 3 months post-treatment * A selection of participants will also be invited to focus group interviews with the aim to generate ideas on how the intervention may be improved for future use
Trial Details
NCT Number NCT06661460
Lead Sponsor Lund University
Conditions
(from sponsor)
ANXIETY DISORDERS (or Anxiety and Phobic Neuroses), Specific Phobia, Social Anxiety Disorder, Separation Anxiety Disorder, Generalized Anxiety Disorder, Panic Disorder, Agoraphobia
Related terms Agoraphobia, Anxiety Disorders, Anxiety, Separation, Generalized Anxiety Disorder, Panic Disorder, Phobia, Social, Phobia, Specific, Phobic Disorders
Enrollment 48 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov