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Development of Transdiagnostic Single-session Treatment

L

Luleå Tekniska Universitet

Status

Enrolling

Conditions

Stress Disorder
Depression
Anxiety Disorders

Treatments

Behavioral: Transdiagnostic single-session treatment

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this clinical trial is to test a single session treatment program in primary care patients with anxiety and/or depression and/or stress-related issues. The main questions it aims to answer is:

  • Will the transdiagnostic treatment program decrease symptoms of depression/anxiety/stress?
  • Will the transdiagnostic treatment program decrease transdiagnostic risk factors?
  • Will the transdiagnostic treatment program decrease the measured risk factors equally?
  • Will the transdiagnostic treatment program impact patients with anxiety, depression or stress disorders equally?
  • Will the transdiagnostic treatment program have long term (6 months post-treatment) effect on transdiagnostic risk factors?
  • Will the transdiagnostic treatment program have long term (6 months post-treatment) effect on anxiety, depression, or stress-symptoms?
  • Have the participants been able to generalize the skills taught in the program(qualitative)?
  • Within group that were treated with single-session treatment and recieved additional care before follow-up, was there a difference in outcome?

Full description

The study investigates the effect of a single-session, 4 hour, transdiagnostic treatment for primary care patientst with depression, anxiety or stress.

The treatment includes, interoceptive exposure, behavioral activation, mindfulness, defusion and psycho-education about emotions.

The study is conducted in a clinical setting in northern sweden and follows up results at 3 weeks and 6 months post treatment.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Meet the criteria for anxiety, mood disorder, or stress diagnosis
  • Symptoms are mild to moderate in severity

Exclusion criteria

  • Already in ongoing psychotherapy
  • Within a month commenced pharmaceutical treatment that will likely impact mood or psychological functioning and is not deemed to be on a stable dose
  • Has a comorbid personality disorder
  • Has a risk of suicide deemed other than low
  • Has other severe psychological disorders outside the scope of primary care
  • Is in a severely stressful social situation deemed incompatible with psychotherapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 2 patient groups

Control group
No Intervention group
Treatment group
Experimental group
Description:
Transdiagnostic single-session treatment
Treatment:
Behavioral: Transdiagnostic single-session treatment

Trial contacts and locations

1

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Central trial contact

John Näsling, Master

Data sourced from clinicaltrials.gov

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