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CompletedNCT03113175Updated Feb 4, 2026

Collabri Flex - Effect of Collaborative Care for People With Anxiety Disorders in General Practice

An interventional study of Collaborative care and Consultations-Liaison in Panic Disorder, Generalized Anxiety Disorder and Social Phobia, sponsored by Amager Hospital. Completed at 1 site in Denmark. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-04.

Sponsored by Amager Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
302
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The aim of the study Collabri Flex is to:

  • Develop a Danish model for collaborative care for patients with anxiety in general practice, based on past experience gained in the Collabri Project.
  • Examine the impact of this model compared with liaison-consultation for people with anxiety in a randomized controlled design from selected endpoints.
Read the detailed description

The Collabri Flex model for Collaborative Care takes point of departure in the earlier study Collabri. It is changed according to gathered information under the first study of the Collabri model in order to achieve a Danish Collaborative Care model easier to implement.

The aims of Project Collabri Flex are to:

  • Develop a flexible model for collaborative care (the Collabri Flex model) for patients with anxiety.
  • Study the effects of this Collabri Flex model against consultation liaison in a randomized design on selected outcomes.

In Collabri the treatment is in line with a set of general treatment principles relevant for collaborative care interventions. The patients in the intervention group are offered cognitive behavioral therapy (CBT), psychoeducation and medication according to at stepped care model by a care manager refering to the general practitioner.

The Collabri Flex study is set up as a researcher-blinded individually randomized controlled trial with participation of an intervention group (treatment according to the Collabri Flex model) and a consultation liaison group.

This study will contribute with new knowledge on collaborative care interventions in a Scandinavian context.

02

Conditions studied

  • Panic Disorder
  • Generalized Anxiety Disorder
  • Social Phobia
  • Obsessive-Compulsive Disorder
  • Post Traumatic Stress Disorder
  • Agoraphobia

Keywords

  • Anxiety
  • Collaborative care
  • Consultation-liaison
  • General practitioner
  • Psychiatry
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age: 18+ years
  • Danish speaking
  • Diagnosis of current anxiety in the form of panic disorder, generalized anxiety, PTSD, agoraphobia, OCD or social phobia based on the Mini International Neuropsychiatric Interview (MINI) by care manager that have been trained in using MINI. Patients can be referred from the GP on the basis of panic disorder, generalized anxiety, social phobia, OCD, PTSD, agoraphobia or depression diagnosis
  • The patient has given her/his written informed consent to participate in the trial at the described terms.

Exclusion criteria

Exclusion Criteria:

  • High risk of suicide assessed in the Mini International Neuropsychiatric Interview (MINI) and/or by the GP
  • Psychotic condition assessed in the MINI and/or by the GP
  • Patients with a diagnosis of dementia
  • Alcohol or substance misuse that will hinder the person's participation in Collabri treatment assessed by the practitioner or care manager at inclusion interview
  • If the patient has been referred or is recommended referral to secondary care treatment (mental health center) or psychiatrist in private practice
  • Patients who are assessed by the GP as medically unstable making it impossible for the patient to adhere to treatment
  • Bipolar affective disorder as assessed in the MINI and/or by the GP
  • Pregnancy

For patients in the Collabri Flex group:

  • Patients with depression who wants treatment cf. the psychologist scheme (Psykologordningen) or similar treatment and do not want the refferal to the psychologist preceded by other treatment, cf. the Collabri Flex model assessed by the GP
  • Patients that wish to continue current psychological or psychiatric treatment due to anxiety or depression
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
302 participants (actual)

Study arms

  • Experimental
    Collabri Flex

    Collaborative care

    Behavioral: Collaborative care

  • Experimental
    Consultation-Liaison

    Consultations with general practitioner

    Behavioral: Consultations-Liaison

Interventions

  • BehavioralCollaborative care

    Collaborative care provided by the general practitioner and the care manager. Treatment modalities: Cognitive-behavior Therapy, psychoeducation, medication according to a stepped care model

  • BehavioralConsultations-Liaison

    Consultation-Liaison provided by general practitioner involving a educational relationship with the Collabri Flex team (care manager and psychiatrist).

05

What researchers measure

Primary outcomes

  1. Self-reported degree of anxiety

    Measured by Beck Anxiety Inventory (BAI)

    Time frame: 6 months

Secondary outcomes

  1. Self-reported degree of depression

    Measured by Beck Depression Inventory (BDI-II)

    Time frame: 6 months

  2. Self-reported pychological stress

    Measured by the Symptom Checklist SCL-90-R

    Time frame: 6 months

  3. Self-reported functional impairment

    Measured by Sheehan Disability Scale (SDS)

    Time frame: 6 months

  4. Self-reported quality of life/well-being

    Measured by WHO-5

    Time frame: 6 months

Other outcomes

  1. Sick leave

    Obtained from the DREAM database

    Time frame: 6 months

  2. Sick leave

    Obtained from the DREAM database

    Time frame: 18 months

  3. Self-reported self-efficacy

    Measured by the IPQ-R Scale (Personal control) and two subscales from the Chronic disease Selv-Efficacy Scales (SECD-32); Obtain help from Community, Family, Friends Scale and control Manage Depression Scale

    Time frame: 6 months

  4. Self-reported self-efficacy

    Measured by the IPQ-R Scale (Personal control) and two subscales from the Chronic disease Selv-Efficacy Scales (SECD-32); Obtain help from Community, Family, Friends Scale and control Manage Depression Scale

    Time frame: 18 months

  5. Self-reported health-related quality of life

    Measured by EQ-5D

    Time frame: 6 months

  6. Self-reported health-related quality of life

    Measured by EQ-5D

    Time frame: 18 months

  7. Employment

    Obtained from the DREAM database

    Time frame: 6 months

  8. Employment

    Obtained from the DREAM database

    Time frame: 18 months

  9. Mental-health outpatient services

    National patient register

    Time frame: 6 months

  10. Mental-health outpatient services

    National patient register

    Time frame: 18 months

  11. Experience of support in recovery

    Self-reported support in recovery (INSPIRE)

    Time frame: 6 months

  12. Patient satisfaction

    Self-reported satisfaction with treatment (CSQ-8)

    Time frame: 6 months

  13. Self-reported degree of anxiety

    Measured by Beck Anxiety Inventory (BAI)

    Time frame: 18 months

  14. Self-reported degree of depression

    Measured by Beck Depression Inventory (BDI-II)

    Time frame: 18 months

  15. Self-reported pychological stress

    Measured by the Symptom Checklist SCL-90-R

    Time frame: 18 months

  16. Self-reported functional impairment

    Measured by Sheehan Disability Scale (SDS)

    Time frame: 18 months

  17. Self-reported quality of life/well-being

    Measured by WHO-5

    Time frame: 18 months

06

Study locations

1 site
  • Mental Health Centre Copenhagen
    Copenhagen, Denmark
07

References and documents

Publications

  • Curth NK, Bjorkedal STB, Hjorthoj C, Brinck-Claussen U, Jorgensen KB, Rosendal S, Bojesen AB, Nordentoft M, Eplov LF. Collaborative Care Versus Consultation Liaison for Patients With Depression or Anxiety Disorders in General Practice in Denmark: 18-Month Follow-Up From the Collabri Flex Trials. Depress Anxiety. 2025 Jun 5;2025:2909617. doi: 10.1155/da/2909617. eCollection 2025. PubMed 40510804 ↗
  • Curth NK, Hjorthoj C, Brinck-Claussen U, Jorgensen KB, Rosendal S, Bojesen AB, Nordentoft M, Eplov LF. The effects of collaborative care versus consultation liaison for anxiety disorders and depression in Denmark: two randomised controlled trials. Br J Psychiatry. 2023 Sep;223(3):430-437. doi: 10.1192/bjp.2023.77. PubMed 37395101 ↗
  • Curth NK, Brinck-Claussen U, Jorgensen KB, Rosendal S, Hjorthoj C, Nordentoft M, Eplov LF. Collaborative care vs consultation liaison for depression and anxiety disorders in general practice: study protocol for two randomized controlled trials (the Danish Collabri Flex trials). Trials. 2019 Oct 25;20(1):607. doi: 10.1186/s13063-019-3657-0. PubMed 31653228 ↗

Individual participant data

Plan to share: Undecided

08

Registry details

Key details

Study ID
NCT03113175
Lead sponsor
Amager Hospital
Responsible party
Lene Falgaard Eplov (Head of Research, Associate professor, Amager Hospital) — Principal investigator
First posted
Apr 13, 2017
Start date
Jan 15, 2018
Primary completion
Mar 29, 2021
Completion
Mar 29, 2021
Last update
Feb 4, 2026

Study contacts

Lene Falgaard Eplov, MD,PhD
principal investigator · Research Unit, Mental Health Center Copenhagen

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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