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Completed

NCT Number: NCT02044913

Randomized-controlled Trial of Aftercare-Coordination by Phone for Depression and Anxiety

The primary objective of this study is to test in a randomized controlled trial if aftercare-coordination by phone subsequent to inpatient treatment is an effective aftercare approach in the treatment of depression and anxiety.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Medical Center Hamburg-Eppendorf, Centre of Psychosocial Medicine, Department of Medical Psychology

Hamburg, Germany

About this study

Depression and anxiety are among the most prevalent mental health problems and are associated with a high risk of chronification. Despite the large capacities in the German health care system only a small percentage of these patients receive treatment. Relevant barriers on the pathways of patients are communication und coordination difficulties between different services and providers.The aftercare subsequent to an inpatient treatment represents one of these interfaces. Here the aim is to consolidate the treatment outcomes and to minimize the so called rebound-effect, the reduction of the positive treatment effects after the inpatient treatment. Although evidence-based treatments for depression and anxiety disorders exist, treatment effects often decrease after treatment due to the lack of an integration of different steps in care. The method of a case management-based aftercare coordination by phone could be a promising approach to overcome the interface between inpatient treatment and aftercare: case management is a patient-centered and situation-based approach which comprises systematic tracking and support of patients by a case-manager. Primary goal is to coordinate and integrate services across treatment settings. This approach can help to maintain and even improve longterm treatment outcomes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Depressive disorder (F32.x; F33.x; F34.1) and/or Anxiety disorder (F40.0; F40.1, F41.0; F41.1) according to ICD-10

Exclusion criteria

  • Concurrent outpatient psychotherapeutic treatment which will be continued after the inpatient rehabilitation treatment.
  • No knowledge of the German language
  • Risk of suicide
  • Acute psychosis or psychotic symptoms

Treatment and study plan

Phone-based Aftercare-Coordination

Behavioral

After inpatient treatment patients receive six phone contacts of aftercare-coordination at intervals of two weeks carried out by therapists for 12 weeks. The intervention is case-management orientated and aims at supporting the patients in finding and organising an adequate aftercare treatment.

Primary outcomes

  1. Measure of the symptom severity - Beck Depression Inventory (BDI)

    Time frame: Change in the BDI from the beginning of the intervention to follow up (6 months after termination of the intervention)

Secondary outcomes

  1. Measure of health related quality of life - Short Form 8 Health Survey (SF-8), Measure of health related quality of life (EQ-5D)

    Time frame: Change in the SF-8 and EQ-5D from the beginning of the intervention to follow up (6 months after termination of the intervention)

  2. Proportion of patients who get routine outpatient aftercare treatment at follow up (6 months after the intervention)

    Time frame: 6 months after termination of the intervention

  3. Patient-rated acceptance and satisfaction with the intervention

    Time frame: Approximately 3 months (end of intervention)

    Patients rate their acceptance of the intervention and their satisfaction using non-standardized items.

Sponsors and collaborators

Lead sponsor

Universitätsklinikum Hamburg-Eppendorf

Other

Registry information

Official study title

Randomized-controlled Trial of Aftercare-Coordination by Phone for Patients With Depression and Anxiety Subsequent to an Inpatient Treatment.

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Jan 24, 2014
Registry last updated
Jul 15, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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