Actively Recruiting
Guided Internet-delivered Treatment for Moderate Depression, Social Anxiety Disorder and Panic Disorder - An Open Naturalistic Multicentre Cost-effectiveness Trial
Led by St. Olavs Hospital · Updated on 2025-06-05
800
Participants Needed
4
Research Sites
74 weeks
Total Duration
On this page
Sponsors
S
St. Olavs Hospital
Lead Sponsor
H
Haukeland University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness and cost-effectiveness of a therapist-guided internet-based cognitive behavioral therapy (ICBT) program called eMeistring. This program targets adults with moderate depression, social anxiety disorder, and panic disorder in routine healthcare settings. The study aims to understand who benefits from the treatment, predictors of drop-out, and how user experience affects adherence and outcomes across multiple clinics. Participants receive up to nine guided ICBT sessions delivered online, with weekly therapist support via secure email. The treatment starts with an initial face-to-face visit, followed by the online modules, and concludes with a final face-to-face session. Therapists involved are licensed healthcare professionals such as psychologists and social workers. The program is integrated as standard care at four hospital locations, and patients enter through usual clinical pathways. During the study, participants complete questionnaires on symptom severity, quality of life, work and social function, medication use, and satisfaction at several points: before treatment, up to 14 weeks after starting, six months later, and after two years. Routine clinical follow-up monitors any adverse events, including suicidal behavior alerts. Researchers will analyze effectiveness, adherence, drop-out predictors, and cost-effectiveness across clinics and patient groups over the study period.
CONDITIONS
Brief Title
Effects and Cost-effectiveness of e-Meistring - a Guided Internet-delivered Psychological Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Diagnosed with moderate depression, panic disorder, or social anxiety disorder as the primary condition
- Access to a computer and internet
You will not qualify if you...
- Having severe depression
- Experiencing suicidal impulses or thoughts
- Diagnosed with bipolar disorder or psychosis
- Substance abuse
- Having unstable medication in the last month
- Severe reading or writing disabilities
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 pre-treatment assessment visit (in-person)
Duration - Up to 14 weeks
Participants receive therapist-guided internet-based cognitive behavioral therapy (ICBT) consisting of eight to nine weekly sessions or modules, with therapist guidance provided at least once a week via secure email. The treatment starts with an initial face-to-face visit and ends with a final face-to-face visit.
1 initial face-to-face visit, weekly online sessions with therapist guidance, and 1 final face-to-face visit
Duration - Up to 2 years after treatment
Participants are followed up with assessments at six months and two years after treatment completion to evaluate ongoing outcomes.
Assessments at 6 months and 2 years post-treatment (may be in-person or remote)
Trial Site Locations
Total: 4 locations
1
Helse Bergen HF
Bergen, Norway
Actively Recruiting
2
Sykehuset Innlandet HF
Lillehammer, Norway
Actively Recruiting
3
St. Olavs Hospital HF
Trondheim, Norway
Actively Recruiting
4
Sykehuset i Vestfold HF
Tønsberg, Norway
Actively Recruiting
Research Team
V
Vidar Halsteinli, PhD
J
Jørn Heggelund, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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