NCT05016843

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,477

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2021

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
15 days until next milestone

First Posted

Study publicly available on registry

August 23, 2021

Completed
2 days until next milestone

Study Start

First participant enrolled

August 25, 2021

Completed
4.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 22, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 22, 2026

Completed
Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

4.4 years

First QC Date

August 8, 2021

Last Update Submit

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.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Unified protocolOther: Treatment length: 8 weeksOther: Access to a moderated forum

CBT, 16 weeks and access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Unified protocolOther: Treatment length: 16 weeksOther: No access to a moderated forum

CBT, 8 weeks and no access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Unified protocolOther: Treatment length: 8 weeksOther: No access to a moderated forum

CBT, 16 weeks and no access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Unified protocolOther: Treatment length: 16 weeksOther: Access to a moderated forum

Psychodynamic therapy, 8 weeks and access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Affect phobia treatmentOther: Treatment length: 8 weeksOther: Access to a moderated forum

Psychodynamic therapy, 16 weeks and access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Affect phobia treatmentOther: Treatment length: 16 weeksOther: Access to a moderated forum

Psychodynamic therapy, 8 weeks and no access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Affect phobia treatmentOther: Treatment length: 8 weeksOther: No access to a moderated forum

Psychodynamic therapy, 16 weeks and no access to forum.

EXPERIMENTAL
Behavioral: Treatment condition: Internet-administered Affect phobia treatmentOther: Treatment length: 16 weeksOther: No access to a moderated forum

Waitlist, 8 weeks and access to forum.

EXPERIMENTAL
Other: Treatment condition: Waitlist controlOther: Treatment length: 8 weeksOther: Access to a moderated forum

Waitlist, 16 weeks and access to forum.

EXPERIMENTAL
Other: Treatment condition: Waitlist controlOther: Treatment length: 16 weeksOther: Access to a moderated forum

Waitlist, 8 weeks and no access to forum.

EXPERIMENTAL
Other: Treatment condition: Waitlist controlOther: Treatment length: 8 weeksOther: No access to a moderated forum

Waitlist, 16 weeks and no access to forum.

EXPERIMENTAL
Other: Treatment condition: Waitlist controlOther: Treatment length: 16 weeksOther: No access to a moderated forum

Interventions

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.

CBT, 16 weeks and access to forum.CBT, 16 weeks and no access to forum.CBT, 8 weeks and access to forum.CBT, 8 weeks and no access to forum.

The waitlist condition is a control condition without any intervention.

Waitlist, 16 weeks and access to forum.Waitlist, 16 weeks and no access to forum.Waitlist, 8 weeks and access to forum.Waitlist, 8 weeks and no access to forum.

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.

Psychodynamic therapy, 16 weeks and access to forum.Psychodynamic therapy, 16 weeks and no access to forum.Psychodynamic therapy, 8 weeks and access to forum.Psychodynamic therapy, 8 weeks and no access to forum.

Participants will partake in their treatment condition for 8 weeks.

CBT, 8 weeks and access to forum.CBT, 8 weeks and no access to forum.Psychodynamic therapy, 8 weeks and access to forum.Psychodynamic therapy, 8 weeks and no access to forum.Waitlist, 8 weeks and access to forum.Waitlist, 8 weeks and no access to forum.

Participants will partake in their treatment condition for 16 weeks.

CBT, 16 weeks and access to forum.CBT, 16 weeks and no access to forum.Psychodynamic therapy, 16 weeks and access to forum.Psychodynamic therapy, 16 weeks and no access to forum.Waitlist, 16 weeks and access to forum.Waitlist, 16 weeks and no access to forum.

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.

CBT, 16 weeks and no access to forum.CBT, 8 weeks and access to forum.Psychodynamic therapy, 16 weeks and access to forum.Psychodynamic therapy, 8 weeks and access to forum.Waitlist, 16 weeks and access to forum.Waitlist, 8 weeks and access to forum.

Participants will not have access to a moderated forum, hence their treatment is self-guided.

CBT, 16 weeks and access to forum.CBT, 8 weeks and no access to forum.Psychodynamic therapy, 16 weeks and no access to forum.Psychodynamic therapy, 8 weeks and no access to forum.Waitlist, 16 weeks and no access to forum.Waitlist, 8 weeks and no access to forum.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

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.

  • Hlynsson 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.

MeSH Terms

Conditions

Anxiety DisordersDepression

Condition Hierarchy (Ancestors)

Mental DisordersBehavioral SymptomsBehavior

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

Locations