Actively Recruiting

Age: 18Years +
All Genders
ID05868135

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 pre-treatment assessment visit (in-person)

Treatment

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

Follow-up

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

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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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