Project Collabri for Treatment of Anxiety

Sponsor
Mental Health Centre Copenhagen (Other)
Overall Status
Completed
CT.gov ID
NCT02678624
Collaborator
(none)
406
1
2
68
6

Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether treatment of patients with anxiety according to the Collabri Model is more effective in reducing symptoms compared to treatment as usual (TAU)

Condition or Disease Intervention/Treatment Phase
  • Other: Treatment according to the Collabri model
N/A

Detailed Description

Background:

Depression and anxiety are common diseases often treated in general practice. However, there are obstacles for optimal treatment e.g. a lack of continuity in disease management, organized collaboration between primary and secondary care and access to psychotherapy. Previous collaborative care studies have shown significant improvements in treatment outcomes for patients with depression and anxiety in primary care; however studies have yet not been carried out in a Danish context. Thus, the Collabri-model for collaborative care for panic disorder, generalized anxiety, social phobia and depression has been developed. The model includes: a multi-professional approach to treatment including a care manager (e.g. a psychiatric nurse), enhanced inter-professional communication, scheduled monitoring and review and structured treatment plans.

Objective:

To investigate whether treatment according to the Collabri-model have an effect on symptoms for people with anxiety disorders.

Methods/design:

Three cluster-randomized, clinical trials are set up to investigate treatment according to the Collabri-model compared to treatment as usual for 364 patients diagnosed with panic disorder, generalized anxiety and social phobia respectively from general practices in the Capital Region of Denmark. For all studies, the primary outcome is anxiety symptoms measured with Beck Anxiety Inventory (BAI) at 6 months.

Results/discussion:

The results will contribute new knowledge on collaborative care for depression and anxiety disorders in Danish conditions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
406 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Project Collabri. The Effects of a Danish Model of Collaborative Care for People With Anxiety in General Practice
Actual Study Start Date :
Nov 1, 2014
Actual Primary Completion Date :
Jul 1, 2017
Actual Study Completion Date :
Jul 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment according to the Collabri model

Participants in this group will recive treatment according to the Collabri model which is a Danish model for collaborative care between primary and secondary care for depression, social phobia, generalized anxiety and panic disorder

Other: Treatment according to the Collabri model
The Collabri Model is a complex intervention and consists of a number of treatment modalities. The Collabri Model includes the following elements: A multi-professional approach to treatment including a care manager, scheduled monitoring and review, enhanced inter-professional communication and a structured treatment plan. It further integrates: Recruitment of staff with psychiatric experience, training of general practitioner and care manager, use of instruments for detection and follow-up, education and treatment of the patient, supervision from a psychiatric specialist, guided self-help, patient- and relative involvement and a stepped care approach to treatment where treatment is always commenced on the least invasive and least resource-demanding level.

No Intervention: Treatment as usual

Control group. Participants in this group will recive treatment as usual. This means that participants will recive treatment corresponding to what their GP normally would offer as treatment. E.g. this could be refferal to a psychologist or psychiatrist and/or medicine.

Outcome Measures

Primary Outcome Measures

  1. Degree of anxiety measured by the Beck Anxiety Inventory (BAI) [At 6 months follow up after baseline]

    The measure is self-reported

Secondary Outcome Measures

  1. Degree of depression measured by the Beck Depression Inventory (BDI) [At 6 months follow up after baseline]

    The measure is self-reported

  2. Psychological stress measured with the Symptom Checklist (SCL-92) [At 6 months follow up after baseline]

    The measure is self-reported

  3. Functional impairment measured with the Global Assessment of Functioning (GAF-F split version) [At 6 months follow up after baseline]

    The measure is obtained through a semi-structured interview

Other Outcome Measures

  1. Degree of anxiety measured by the Beck Anxiety Inventory (BAI) [At 15 months follow up after baseline]

    The measure is self-reported

  2. Degree of depression measured by the Beck Depression Inventory (BDI) [At 15 months follow up after baseline]

    The measure is self-reported

  3. Psychological stress measured with the Symptom Checklist (SCL-92) [At 15 months follow up after baseline]

    The measure is self-reported

  4. Functional impairment measured with the Global Assessment of Functioning (GAF-F split version) [At 15 months follow up after baseline]

    The measure is obtained through a semi-structured interview

  5. Quality of life measured with the WHO-5 scale [At 6 months follow up after baseline]

    The measure is self-reported

  6. Quality of life measured with the WHO-5 scale [At 15 months follow up after baseline]

    The measure is self-reported

  7. Personal and social performance measured with the Personal and Social Performance scale (PSP) [At 6 months follow up after baseline]

    The measure is obtained through a semi-structured interview

  8. Personal and social performance measured with the Personal and Social Performance scale (PSP) [At 15 months follow up after baseline]

    The measure is obtained through a semi-structured interview

  9. Side effects measured by the PRISE questionnaire [At 6 months follow up after baseline]

    The measure is self-reported

  10. Side effects measured by the PRISE questionnaire [At 15 months follow up after baseline]

    The measure is self-reported

  11. Health-related quality of life measured with the EQ-5D [At 6 months follow up after baseline]

    The measure is self-reported

  12. Health-related quality of life measured with the EQ-5D [At 15 months follow up after baseline]

    The measure is self-reported

  13. Functional impairment measured with Sheehan Disability Scale (SDS) [At 6 months follow up after baseline]

    The measure is self-reported

  14. Functional impairment measured with Sheehan Disability Scale (SDS) [At 15 months follow up after baseline]

    The measure is self-reported

  15. Sick leave [At 6 months follow up after baseline]

    The measure is obtained from the Danish DREAM database

  16. Sick leave [At 15 months follow up after baseline]

    The measure is obtained from the Danish DREAM database

  17. Self-efficacy measured with the subscale "Obtain Help from Community, Family, Friends" from the Chronic Disease Self-Efficacy Scale [At 6 months follow up after baseline]

    The measure is self-reported

  18. Self-efficacy measured with the subscale "Obtain Help from Community, Family, Friends" from the Chronic Disease Self-Efficacy Scale [At 15 months follow up after baseline]

    The measure is self-reported

  19. Self-efficacy measured with the subscale "Control/Manage Depression Scale" from the Chronic Disease Self-Efficacy Scale [At 6 months follow up after baseline]

    The measure is self-reported

  20. Self-efficacy measured with the subscale "Control/Manage Depression Scale" from the Chronic Disease Self-Efficacy Scale [At 15 months follow up after baseline]

    The measure is self-reported

  21. Self-efficacy measured with the subscale "Personal Control" from The Revised Illness Perception Questionnaire (IPQ-R) [At 6 months follow up after baseline]

    The measure is self-reported

  22. Self-efficacy measured with the subscale "Personal Control" from The Revised Illness Perception Questionnaire (IPQ-R) [At 15 months follow up after baseline]

    The measure is self-reported

  23. Apathia [At 6 months follow up after baseline]

    The measure is obtained through a semi-structured interview

  24. Apathia [At 15 months follow up after baseline]

    The measure is obtained through a semi-structured interview

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age: 18+ years

  • Danish speaking

  • Diagnosis of current depression using the Mini International Neuropsychiatric Interview (MINI) (DSM IV) by researchers that have been trained in using MINI and according to the ICD-10 criteria or when diagnosed by GP after conference with a psychiatrist in Project Collabri

  • The patient has given her/his written informed consent to participate in the trial at the described terms

Exclusion Criteria:
  • High risk of suicide assessed in the Mini International Neuropsychiatric Interview (MINI) and/or by general practitioner

  • Psychotic condition detected in the MINI and/or by general practitioner

  • Patients with a diagnosis of dementia

  • Pregnancy

  • Alcohol or substance misuse that hinders the person participating in Collabri treatment as assessed by the practitioner or researcher at inclusion interview

  • Patients that are in current psychological or psychiatric treatment due to anxiety or depression

  • Patients with a pending disability pension case

  • Patients who have been treated for anxiety or depression within the last 6 months

  • For patients in the intervention group: Patients with depression who wants treatment cf. the Danish psychologist scheme and do not want the reference to the psychologist preceded by other treatment, cf. the Collabri model

  • For patients in the intervention group: If the patient at the first point of contact with the general practitioner after inclusion by a research assistant is referred to treatment as a part of the secondary psychiatric care system.

  • Patients who are assessed by the general practitioner as medically unstable making it impossible for the patient to adhere to treatment

  • OCD, PTSD, bipolar affective disorder as assessed in the MINI and/or by the general practitioner

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mental Health Centre Copenhagen Copenhagen Denmark

Sponsors and Collaborators

  • Mental Health Centre Copenhagen

Investigators

  • Principal Investigator: Lene F Eplov, MD PhD, Mental Health Center Copenhagen

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mental Health Centre Copenhagen
ClinicalTrials.gov Identifier:
NCT02678624
Other Study ID Numbers:
  • H-3-2013-203-A
First Posted:
Feb 10, 2016
Last Update Posted:
Sep 13, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2021