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Effectiveness and Cost-effectiveness of Telephone-delivered Psychotherapy for Depression in Primary Care

Primary Purpose

Depression

Status
Unknown status
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Tel-PT
TAU and text messages
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depression focused on measuring mild and moderate depression

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • PHQ-9 score of > 5 and ≤15.
  • Informed Consent as documented by signature (Appendix Informed Consent Form)
  • Minimum age of 18 years
  • Diagnosis of mild to moderate depression according to ICD-10 (F32.0, F32.1, F33.0, F33.1)

Exclusion Criteria:

  • Patients currently being in psychotherapeutic treatment or treatment in past three months
  • Suicidal tendencies or suicidality
  • Insufficient knowledge of German language
  • Health condition that does not allow questionnaire completion

Sites / Locations

  • University of Zurich

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tel-PT

TAU and text messages

Arm Description

Tel-PT receives a manualized short-term CBT. Treatment consists of one initial face-to-face appointment and 8-12 subsequent telephone sessions between patient and licensed therapist. Each telephone contact lasts between 20 and 30 minutes and take place on a weekly and later biweekly basis.

Control Group receives treatment as usual and additionally weekly text messages containing general information about depression.

Outcomes

Primary Outcome Measures

Change in depressive symptoms
The change in depressive symptoms will be assessed with the German version of Patient Health Questionnaire (PHQ-9; Löwe, Spitzer, Zipfel, & Herzog 2002).

Secondary Outcome Measures

Change in depressive symptoms
The change in depressive symptoms will be assessed with the German version of Patient Health Questionnaire (PHQ-9; Löwe, Spitzer, Zipfel, & Herzog 2002).
Response
Response defined as 50% reduction in the PHQ-9.
Change in health-related quality of life
Change in health-related quality of life is measured with the 12-Item Short Form Health Survey (SF-12; Bullinger & Kirchberger, 1998).
Self-efficacy for management and relapse prevention in depression
Depression self-efficacy scale for management and relapse prevention (Bush et al., 2001).
Cost-effectiveness
Health care utilization and productivity loss will be measured with an adapted version of the Client Sociodemographic and Service Receipt Inventory (CSSRI; Chisholm et al., 2000). For Switzerland, country-specific unit costs will be employed to calculate direct and indirect costs.
Cost-effectiveness
Health-related quality of life for the economic analyses will be measured using the EQ-5D-5L (The EuroQuol Group, 1990), Quality-adjusted life years (QALYs) based on the EQ-5D index will be determined and the incremental cost-effectiveness ratio (ICER) will be computed.

Full Information

First Posted
December 3, 2015
Last Updated
October 11, 2018
Sponsor
University of Zurich
Collaborators
Universitätsklinikum Hamburg-Eppendorf
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1. Study Identification

Unique Protocol Identification Number
NCT02667366
Brief Title
Effectiveness and Cost-effectiveness of Telephone-delivered Psychotherapy for Depression in Primary Care
Official Title
Improving Access to Evidence-based Treatment for Depression: Effectiveness and Cost-effectiveness of Telephone-delivered Cognitive Behavioral Therapy (CBT) in Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
March 2019 (Anticipated)
Study Completion Date
March 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich
Collaborators
Universitätsklinikum Hamburg-Eppendorf

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is the examination of effectiveness and cost-effectiveness of a telephone-based psychotherapy (Tel-PT) for depression compared to treatment as usual in primary care.
Detailed Description
The overall purpose of the study is to examine the effectiveness of telephone psychotherapy (Tel-PT) for the treatment of mild to moderate depression on different outcome-levels and under clinically representative conditions in Swiss primary health care. The randomized-controlled trial (RCT) will evaluate the primary hypothesis that Tel-PT is more effective than routine primary care (i.e. treatment as usual, TAU), more specifically, that it leads to significant higher reduction in depression severity than TAU at follow-up. The intervention group (IG) receives a manualized short-term cognitive behavioral treatment, which is the adapted German version of the program "Creating a balance" developed in the USA. The therapy consists of one face-to-face and 8-12 telephone contacts and is carried out by a licensed psychotherapist. More concrete, recruitment and inclusion of the patients will be carried out by the participating general practitioners (GPs). GPs will be instructed to screen patients at risk for depression, especially those revealing diffuse somatic symptoms and suffering from chronic diseases. If positively screened, patient's depressive symptoms are assessed with Patient Health Questionnaire (PHQ-9) and diagnosed according to ICD-10. All GPs will receive an initial training prior to their participation, providing them with study information and procedures as well as training in screening procedure, psychodiagnostics and study enrolment. Eligible patients are provided with detailed study information and asked to participate. Subsequently, patients will give informed consent. Patients will then be included into the study and fill out the baseline questionnaires (t0). After that, randomization will be carried out at the University of Zurich, based on an appropriately created computer algorithm. Both GPs and patients are informed about the results by the study team within two days. Subsequently, patients in control group (CG) will receive regular text messages and patients in the intervention group (IG) will be called by the study therapist to schedule an initial appointment. In case of positive results, the overarching objective is the optimization of mental health services for depressed patients by implementing an evidence-based, accessible and cost-effective treatment option into primary care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
Keywords
mild and moderate depression

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tel-PT
Arm Type
Experimental
Arm Description
Tel-PT receives a manualized short-term CBT. Treatment consists of one initial face-to-face appointment and 8-12 subsequent telephone sessions between patient and licensed therapist. Each telephone contact lasts between 20 and 30 minutes and take place on a weekly and later biweekly basis.
Arm Title
TAU and text messages
Arm Type
Active Comparator
Arm Description
Control Group receives treatment as usual and additionally weekly text messages containing general information about depression.
Intervention Type
Behavioral
Intervention Name(s)
Tel-PT
Intervention Type
Behavioral
Intervention Name(s)
TAU and text messages
Primary Outcome Measure Information:
Title
Change in depressive symptoms
Description
The change in depressive symptoms will be assessed with the German version of Patient Health Questionnaire (PHQ-9; Löwe, Spitzer, Zipfel, & Herzog 2002).
Time Frame
t0 (baseline) and t2 (12 months after baseline)
Secondary Outcome Measure Information:
Title
Change in depressive symptoms
Description
The change in depressive symptoms will be assessed with the German version of Patient Health Questionnaire (PHQ-9; Löwe, Spitzer, Zipfel, & Herzog 2002).
Time Frame
t0 (baseline) and t1 (four months after baseline)
Title
Response
Description
Response defined as 50% reduction in the PHQ-9.
Time Frame
t0 (baseline), t1 (four months after baseline), t2 (12 months after baseline)
Title
Change in health-related quality of life
Description
Change in health-related quality of life is measured with the 12-Item Short Form Health Survey (SF-12; Bullinger & Kirchberger, 1998).
Time Frame
t0 (baseline), t1 (four months after baseline), t2 (12 months after baseline)
Title
Self-efficacy for management and relapse prevention in depression
Description
Depression self-efficacy scale for management and relapse prevention (Bush et al., 2001).
Time Frame
t0 (baseline), t1 (four months after baseline), t2 (12 months after baseline)
Title
Cost-effectiveness
Description
Health care utilization and productivity loss will be measured with an adapted version of the Client Sociodemographic and Service Receipt Inventory (CSSRI; Chisholm et al., 2000). For Switzerland, country-specific unit costs will be employed to calculate direct and indirect costs.
Time Frame
t0 (baseline), t1 (four months after baseline), t2 (12 months after baseline)
Title
Cost-effectiveness
Description
Health-related quality of life for the economic analyses will be measured using the EQ-5D-5L (The EuroQuol Group, 1990), Quality-adjusted life years (QALYs) based on the EQ-5D index will be determined and the incremental cost-effectiveness ratio (ICER) will be computed.
Time Frame
t0 (baseline), t1 (four months after baseline), t2 (12 months after baseline)
Other Pre-specified Outcome Measures:
Title
Acceptance and satisfaction with the intervention
Description
Patients' and therapists' acceptance and satisfaction with the intervention will be assessed by a self-constructed questionnaire.
Time Frame
t1 (four months after baseline)
Title
Process and structural variable
Description
Mean duration of telephone contacts
Time Frame
t1 (four months after baseline), t2 (12 months after baseline)
Title
Process and structural variable
Description
Mean number of telephone contacts.
Time Frame
t1 (four months after baseline), t2 (12 months after baseline)
Title
Process and structural variable
Description
Dropout rate
Time Frame
t1 (four months after baseline), t2 (12 months after baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PHQ-9 score of > 5 and ≤15. Informed Consent as documented by signature (Appendix Informed Consent Form) Minimum age of 18 years Diagnosis of mild to moderate depression according to ICD-10 (F32.0, F32.1, F33.0, F33.1) Exclusion Criteria: Patients currently being in psychotherapeutic treatment or treatment in past three months Suicidal tendencies or suicidality Insufficient knowledge of German language Health condition that does not allow questionnaire completion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Birgit Watzke, Prof
Organizational Affiliation
University of Zurich, Department of Clinical Psychology and Psychotherapy Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Zurich
City
Zurich
ZIP/Postal Code
8050
Country
Switzerland

12. IPD Sharing Statement

Citations:
Citation
Löwe, B, Spitzer, RL, Zipfel, S, & Herzog, W. Gesundheitsfragebogen für Patienten (PHQ-D): Manual und Testunterlagen. Pfizer. Karlsruhe: 2002.
Results Reference
background
PubMed Identifier
25182269
Citation
Watzke B, Heddaeus D, Steinmann M, Konig HH, Wegscheider K, Schulz H, Harter M. Effectiveness and cost-effectiveness of a guideline-based stepped care model for patients with depression: study protocol of a cluster-randomized controlled trial in routine care. BMC Psychiatry. 2014 Aug 20;14:230. doi: 10.1186/s12888-014-0230-y.
Results Reference
background
PubMed Identifier
15328325
Citation
Simon GE, Ludman EJ, Tutty S, Operskalski B, Von Korff M. Telephone psychotherapy and telephone care management for primary care patients starting antidepressant treatment: a randomized controlled trial. JAMA. 2004 Aug 25;292(8):935-42. doi: 10.1001/jama.292.8.935.
Results Reference
background
Citation
Bush, T, Russo, J, Ludman, E, Lin, E, Von Korff, M, Simon, G, Walker, E. Perceived self-efficacy for depression self-management. A reliable and valid self-report measure with predictive validity: Poster presentation at the American Psychological Society Meeting, June 2001. Toronto, Canada.
Results Reference
background
Citation
Bullinger, M, & Kirchberger, I. Fragebogen zum Gesundheitszustand. Hogrefe. Göttingen: 1998.
Results Reference
background
PubMed Identifier
31597555
Citation
Haller E, Besson N, Watzke B. "Unrigging the support wheels" - A qualitative study on patients' experiences with and perspectives on low-intensity CBT. BMC Health Serv Res. 2019 Oct 9;19(1):686. doi: 10.1186/s12913-019-4495-1.
Results Reference
derived
PubMed Identifier
28724423
Citation
Watzke B, Haller E, Steinmann M, Heddaeus D, Harter M, Konig HH, Wegscheider K, Rosemann T. Effectiveness and cost-effectiveness of telephone-based cognitive-behavioural therapy in primary care: study protocol of TIDe - telephone intervention for depression. BMC Psychiatry. 2017 Jul 19;17(1):263. doi: 10.1186/s12888-017-1429-5.
Results Reference
derived

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Effectiveness and Cost-effectiveness of Telephone-delivered Psychotherapy for Depression in Primary Care

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