Development of a Telephone-based Continuation Treatment for Patients With Chronic Depression.
NCT ID: NCT02397850
Last Updated: 2017-11-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
7 participants
INTERVENTIONAL
2015-02-28
2017-10-25
Brief Summary
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The main purpose of this pilot study is to evaluate the feasibility of a telephone based psychotherapeutic continuation treatment with a small sample of 20 patients suffering from chronic depression. In case of promising results the effectiveness of this kind of treatment is going to be investigated within a comparative trial (including face-to-face intervention, no intervention).
Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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30 min or 50 min
Patients receive either seven 30 minutes or 50 minutes phone calls over 6 months (psychotherapy/continuation treatment)
phone calls 30 min
Patients receive either seven 30 minutes phone calls over 6 months (psychotherapy/continuation treatment)
phone calls 50 min
Patients receive either seven 50 minutes phone calls over 6 months (psychotherapy/continuation treatment)
Interventions
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phone calls 30 min
Patients receive either seven 30 minutes phone calls over 6 months (psychotherapy/continuation treatment)
phone calls 50 min
Patients receive either seven 50 minutes phone calls over 6 months (psychotherapy/continuation treatment)
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of chronic (300.4) or recurrent (296.31-3) depression (according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition)
* Currently in partial or full remission
* Previous psychotherapy (acute treatment; some kind of cognitive-behavioral therapy)
* adequate knowledge of German language
* in case of taking antidepressants: long-term and stable dosage (with unchanged taking since 3 months at least)
Exclusion Criteria
* psychotic symptoms
* severe cognitive impairments
* in case of taking antidepressants: anticipated stopping medication within treatment period (6 months)
18 Years
ALL
No
Sponsors
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University of Zurich
OTHER
Responsible Party
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Principal Investigators
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Birgit Watzke, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
University of Zurich
Locations
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UniversitätsSpital Zürich Klinik für Psychiatrie und Psychotherapie Ambulatorium
Zurich, , Switzerland
Countries
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Other Identifiers
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WATZKE-892
Identifier Type: -
Identifier Source: org_study_id