Online cognitive behavior therapy for common mental disorders in primary care

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized controlled trial aims to evaluate the effectiveness of online transdiagnostic cognitive behavior therapy (CBT) compared to standard care for adult primary care patients with common mental disorders. Participants will be randomly assigned to receive either online CBT, which includes psychoeducation and therapeutic exercises delivered through a secure web platform, or care as usual. The study will assess symptomatic improvement, quality of life, and functional impairment, while also exploring treatment moderators and mediators. The goal is to provide evidence for a more accessible and resource-efficient treatment option for common mental disorders.

Why it matters

Who can join: the full rules

Inclusion Criteria:

To be included patients have to:

1. have a common mental disorder in form of an anxiety disorder (social phobia, panic disorder, agoraphobia, general anxiety disorder, or specific phobia), health anxiety (hypochondriasis or illness anxiety disorder), obsessive-compulsive disorder, depression (depression or dysthymia), or a stress-related disorder (exhaustion disorder, adjustment disorder, or post-traumatic stress disorder), that warrants treatment,
2. be at least 18 years old,
3. have regular access to a device with an Internet connection,
4. be able to read and write in Swedish,
5. have no severe psychiatric disorder that requires specialized psychiatric care, such as psychosis, bipolar disorder, or anorexia nervosa,
6. if on medication with monoamine agonist, have stable dosage in the past month,
7. have no on-going psychological treatment, and
8. provide written informed consent for participation and complete baseline assessment

Where it's running

• Region Stockholm, Gustavsberg Primary Care Center
  Gustavsberg, Stockholm County, Sweden Recruiting

Study contacts

• Principal investigator: Erik Hedman-Lagerlöf, PhD, professor — Region Stockholm and Karolinska Institutet
• Study coordinator: Mari von Bahr Bentzer, MSc.
• Email: mari.vonbahr-bentzer@regionstockholm.se
• Phone: +46 8 123 395 50

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.