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Search / Trial NCT06604845

A Comparison of Group Cognitive Behavioural Therapy (CBT) and Structured Activity Group for Adults With Attention Deficit Hyperactivity Disorder (ADHD)

Launched by VASTRA GOTALAND REGION · Sep 17, 2024

Trial Information

Current as of July 21, 2025

Enrolling by invitation

Keywords

Attention Deficit Hyperactivity Disorder (Adhd) Cognitive Behavioral Therapy Controlled Clinical Trials, Randomized Adults

ClinConnect Summary

Despite medical treatment, many adults with ADHD experience residual symptoms that negatively affect work performance and social life. Hence, several psychological interventions targeting these symptoms have been developed, but the treatment effects are still unclear due to lack of controlled clinical trials.

In this single-blind randomised controlled clinical trial, we will evaluate the effects of group CBT based on Safren's manual "CBT for ADHD/Mastering Your Adult ADHD" (Safren SA et al, Behav Res Ther, 2005), compared to an active control group. The control intervention is a manualised...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria: Fulfilling criteria for ADHD , motivation and practical possibility to participate in the treatment.
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  • Exclusion Criteria: Ongoing psychosis or suicidality, severe self-injury, intellectual disability and insufficient Swedish language skills.
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About Vastra Gotaland Region

Vastra Gotaland Region is a prominent healthcare organization in Sweden, dedicated to advancing medical research and improving patient care through innovative clinical trials. As a sponsor, the region leverages its extensive network of hospitals and healthcare professionals to facilitate high-quality research initiatives that address pressing health challenges. With a commitment to ethical standards and patient safety, Vastra Gotaland Region strives to foster collaboration between researchers, clinicians, and patients, ensuring that clinical trials contribute valuable insights and advancements in medical science.

Locations

Gothenburg, , Sweden

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported