The Study of Internet-delivered, Transdiagnostic Treatments for Anxiety and Depression
TRAbee
1 other identifier
interventional
2,477
1 country
1
Brief Summary
Anxiety and depression are common psychiatric disorders, resulting in suffering and impaired functioning for the individual. Today, most psychological treatments are disorder specific, even tough comorbidity between depression and anxiety and different anxiety disorders is rule rather than exception. Transdiagnostic treatments target the common features between depression and anxiety disorders and has shown to be as effective as disorder specific treatments in reducing symptoms of the disorders. Unified protocol and Affect phobia treatment are two types of transdiagnostic treatments that, to our knowledge, never been compared in research before. Internet-administered treatment presents a promising way to increase availability of psychotherapeutic interventions such as transdiagnostic treatments. However, questions regarding the optimal treatment length and level of support remain unanswered. The aim of this study is to examine two internet-administered transdiagnostic treatments and their effect on anxiety and depression, and to investigate the impact of treatment length and access to a moderated forum. The study will investigate three factors: type of transdiagnostic treatment, length of treatment and whether patients have access to a moderated forum or not. 2400 participants with anxiety and/or depression will be randomly assigned to one of 12 subgroups and subsequently offered treatment based on differing combinations of the previously mentioned factors (200 participants/arm). The treatment conditions are internet-administered cognitive, behavioral treatment (CBT) Unified protocol and the psychodynamic Affect phobia treatment as well as a waitlist control group. Participants will also be randomized to either 8 or 16 weeks of treatment and access to a moderated forum or not. Primary outcome measures will be the Patient Health Questionnaire, the Generalized Anxiety Disorder 7-item scale and the Brief Quality of Life scale. Negative effects of treatment will also be assessed. In addition to pre- and post-treatment measurements, the study includes one mid-treatment and three follow-up assessments (6, 12 and 24 months).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2021
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 8, 2021
CompletedFirst Posted
Study publicly available on registry
August 23, 2021
CompletedStudy Start
First participant enrolled
August 25, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 22, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 22, 2026
CompletedJanuary 26, 2026
January 1, 2026
4.4 years
August 8, 2021
January 22, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Patient Health Questionnaire 9-item scale (PHQ-9)
The PHQ-9 features nine items for assessing depression in a clinical context and screening of depression in the general population.
Through study completion, an average of 2 years.
Generalised Anxiety Disorder 7- item scale (GAD-7)
The GAD-7 features seven items for assessing anxiety and screening for generalized anxiety disorder.
Through study completion, an average of 2 years.
Brunnsviken Brief Quality of Life Scale (BBQ)
The BBQ features 12 items concerning 6 areas of life rated on importance and satisfaction.
Through study completion, an average of 2 years.
Secondary Outcomes (3)
The Personality Inventory for DSM Short Form (PID-5)
Baseline only.
Negative Effects Questionnaire (NEQ)
At post-treatment only (which is week 8 or 16 depending on treatment allocation).
Reflective Functioning Questionnaire 8 (RFQ-8)
Through study completion, an average of 2 years.
Study Arms (12)
CBT, 8 weeks and access to forum.
EXPERIMENTALCBT, 16 weeks and access to forum.
EXPERIMENTALCBT, 8 weeks and no access to forum.
EXPERIMENTALCBT, 16 weeks and no access to forum.
EXPERIMENTALPsychodynamic therapy, 8 weeks and access to forum.
EXPERIMENTALPsychodynamic therapy, 16 weeks and access to forum.
EXPERIMENTALPsychodynamic therapy, 8 weeks and no access to forum.
EXPERIMENTALPsychodynamic therapy, 16 weeks and no access to forum.
EXPERIMENTALWaitlist, 8 weeks and access to forum.
EXPERIMENTALWaitlist, 16 weeks and access to forum.
EXPERIMENTALWaitlist, 8 weeks and no access to forum.
EXPERIMENTALWaitlist, 16 weeks and no access to forum.
EXPERIMENTALInterventions
Treatment condition: The cognitive, behavioral treatment Unified protocol is a transdiagnostic treatment for anxiety and depression. Participants are taught five techniques in order to find new and more helpful ways to react to hindering thoughts and feelings: mindfulness, cognitive flexibility, identify and reduce behavioral avoidance, increase willingness to experience physiological sensations and exposure. The intervention is delivered online through a secure platform. Modules consist of text and the participants can work with the material whenever they wish to. Participants gain access to a new treatment modul every week.
The waitlist condition is a control condition without any intervention.
The aim of psychodynamic Affect phobia treatment is for the patient to reach an intellectual and emotional understanding of his/hers problems. The goal of the treatment is for participants to decrease emotional avoidance and start to approach emotions and increase emotional awareness. Participants are taught this through linking their symptoms to their emotional avoidance, observe frequent and maladaptive patterns in relationships and see how these are linked to emotional avoidance. The intervention is delivered online through a secure platform. Modules consist of text and the participants can work with the material whenever they wish to. Participants gain access to a new treatment modul every week.
Participants will partake in their treatment condition for 8 weeks.
Participants will partake in their treatment condition for 16 weeks.
During their treatment, participants will have access to a discussion forum moderated by a clinician. Participants are encouraged to discuss questions and experiences related to their treatment condition.
Participants will not have access to a moderated forum, hence their treatment is self-guided.
Eligibility Criteria
You may qualify if:
- Be able to read and write Swedish,
- access to a mobile phone/computer,
- years or older,
- GAD-7 ≥ 5 and/or
- PHQ-9 ≥ 10.
You may not qualify if:
- Partaking in other psychological treatment,
- has started or adjusted treatment with psychopharmacological drugs for anxiety, worry or depression within the nearest month,
- severe depression (PHQ-9 ≥ 20) or suicidal (PHQ-9, item 9\>2).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Psychology
Stockholm, Stockholm County, 10691, Sweden
Related Publications (2)
Hlynsson JI, Carlbring P. Diagnostic accuracy and clinical utility of the PHQ-2 and GAD-2: a comparison with long-format measures for depression and anxiety. Front Psychol. 2024 May 10;15:1259997. doi: 10.3389/fpsyg.2024.1259997. eCollection 2024.
PMID: 38800678DERIVEDHlynsson JI, Lindner P, Barri B, Carlbring P. Exploring cutoff points and measurement invariance of the Brunnsviken brief quality of life inventory. Front Psychol. 2024 Jan 8;14:1305682. doi: 10.3389/fpsyg.2023.1305682. eCollection 2023.
PMID: 38259555DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 8, 2021
First Posted
August 23, 2021
Study Start
August 25, 2021
Primary Completion
January 22, 2026
Study Completion
January 22, 2026
Last Updated
January 26, 2026
Record last verified: 2026-01