Evaluation of a Stepped Care Approach to Manage Depression in Diabetes

NCT ID: NCT01812291

Last Updated: 2022-09-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

260 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-02-29

Study Completion Date

2015-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The study examines the efficacy of a stepped care approach for depressed diabetes patients (first study objective). 256 patients with diabetes and comorbid subthreshold or clinical depression will be randomly assigned to either a stepped care approach or a treatment-as-usual condition. The stepped care approach consists of three treatment steps comprising diabetes-specific cognitive-behavioral therapy (CBT) (group), depression-specific CBT (single), and psychotherapeutic and/or psychiatric treatment (single). Patients assigned to the stepped care approach will be treated stepwise until a clinically significant reduction of depressive symptoms is attained or all three treatment steps are passed.

The primary outcome of the first study objective is a clinically significant reduction of depressive symptoms in the 12-month follow-up. Secondary outcomes are reduction of diabetes-related distress and improvement of well-being, health-related quality of life, diabetes acceptance, diabetes self-care, and glycaemic control. Additionally, cost-benefit analyses will be performed.

The second study objective is to analyse associations between diabetes, depression, and the serum levels of inflammatory markers.

The third study objective is to analyse the courses of depressive conditions in diabetes with regard to recovery rates and incidence of major depression.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Compared to persons without diabetes, rates of depressive disorders and mood are doubled in diabetes patients. Epidemiologic studies have shown point prevalence rates of 10 - 14% for major depressive disorder and an additional proportion of almost 20% with subthreshold depression (defined as elevated depressive symptoms without meeting criteria for a specified clinical disorder). Depression and subthreshold depression in diabetes are associated with reduced quality of life, increased diabetes-related distress, and elevated health care costs. Furthermore, depression as well as subthreshold depression seem to be major barriers to an effective self-management of the disease and have been associated with reduced glycaemic control and hyperglycaemia. Both conditions seem to be independent prognostic factors for subsequent morbidity and mortality in diabetes.

Depressive conditions are commonly treated with psychotherapeutic or pharmacologic antidepressive therapies. Since the majority of diabetes patients is suffering from subthreshold depression, evaluated and suitable specific intervention concepts are rare. Moreover, the large variation of symptom levels of depressive patient groups suggests that different types of treatment with different treatment intensities may be required to match individual demands. The issue of 'optimal' treatment also regards concerns about overtreatment and undertreatment of particular patient groups with depressive conditions. Thus, an successive order of treatment steps of increasing intensity appears useful. Since depression in diabetes often is associated with high diabetes-related problems and distress, diabetes-specific as well as depression-specific interventions may be required.

We developed a stepped care approach with three treatment steps comprising diabetes-specific CBT (group), depression-specific CBT (single), and psychotherapeutic and/or psychiatric treatment (single).

The study is a randomized efficacy trial in which the efficacy of the stepped care approach is compared to a treatment-as-usual condition (standard diabetes education). 256 patients with diabetes and comorbid subthreshold or clinical depression will be randomly assigned to either the stepped care approach or the treatment-as-usual condition. Patients assigned to the stepped care approach will be treated stepwise until a clinically significant reduction of depressive symptoms is attained or all three treatment steps are passed.

The primary outcome is a clinically significant reduction of depressive symptoms in the 12-month follow-up. Secondary outcomes are reduction of diabetes-related distress and improvement of well-being, health-related quality of life, diabetes acceptance, diabetes self-care, and glycaemic control. The decisive measurement of this outcomes are conducted 12 months after the treatment (12 month follow up). Additionally, cost-benefit analyses will be performed.

Besides testing the efficacy of the stepped care approach (first objective), there are two additional study objectives:

The second study objective is to analyse associations between diabetes, depression, and the serum levels of inflammatory markers (C-reactive protein (CRP), Interleukin (IL)-6, IL-18, IL-1Ra, Adiponectin, Monocyte chemoattractant protein (MCP)-1). Additionally, the impact of depression treatment on the levels of these markers will be examined.

The third study objective is to analyse the courses of depressive conditions in diabetes with regard to recovery rates and incidence of major depression in subclinically or clinically depressed diabetes patients treated as usual vs. given an intervention.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Major Depressive Disorder Minor Depressive Disorder Sub-Threshold Depression Diabetes Mellitus

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Stepped Care Approach for Depression

Step 1: Diabetes-Specific CBT (5 group sessions)

Step 2: Depression-Specific CBT (6 single sessions)

Step 3: Referral to Psychotherapist and/or Psychiatrist

Group Type EXPERIMENTAL

Step 1: Diabetes-Specific CBT (5 group sessions)

Intervention Type BEHAVIORAL

Diabetes-Specific CBT (5 group sessions) focusing on diabetes-related problems and distress ('DIAMOS - Strengthening Diabetes Motivation').

Includes:

* Diabetes problem analysis/ definition
* Diabetes problem solving intervention
* Cognitive restructuring of diabetes problems
* Activation of personal and social resources
* Goal definition and agreement

Step 2: Depression-Specific CBT (6 single sessions)

Intervention Type BEHAVIORAL

Depression-Specific CBT (6 single sessions) focusing on depressive cognitions and affective problems (manualised).

Includes:

* Functional explanatory model of depression
* Cognitive restructuring of negative thoughts
* Practice of alternative beneficial thoughts
* Specific cognitive interventions regarding self-criticism, guilt, low self-esteem, fear, and inactivity.

Step 3: Referral to Psychotherapist and/or Psychiatrist

Intervention Type BEHAVIORAL

Non-responders to previous treatment steps will be referred to an psychotherapist and/or psychiatrist for intensified treatment. Treatments procedures will be monitored and interventions will be scored to enable the evaluation of treatment effects.

Treatment-as-usual

Standard Diabetes Education

Group Type ACTIVE_COMPARATOR

Standard Diabetes Education

Intervention Type BEHAVIORAL

Standard diabetes education and professional care.

Includes:

* Health care and specific topics (e. g. blood pressure)
* Diabetes complications
* Healthy and unhealthy foods, cooking recommendations and recipes
* Foot care: exercises, care and control, injuries, and diabetic neuropathy
* Sports, activities and exercise
* Social aspects of living with diabetes

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Step 1: Diabetes-Specific CBT (5 group sessions)

Diabetes-Specific CBT (5 group sessions) focusing on diabetes-related problems and distress ('DIAMOS - Strengthening Diabetes Motivation').

Includes:

* Diabetes problem analysis/ definition
* Diabetes problem solving intervention
* Cognitive restructuring of diabetes problems
* Activation of personal and social resources
* Goal definition and agreement

Intervention Type BEHAVIORAL

Step 2: Depression-Specific CBT (6 single sessions)

Depression-Specific CBT (6 single sessions) focusing on depressive cognitions and affective problems (manualised).

Includes:

* Functional explanatory model of depression
* Cognitive restructuring of negative thoughts
* Practice of alternative beneficial thoughts
* Specific cognitive interventions regarding self-criticism, guilt, low self-esteem, fear, and inactivity.

Intervention Type BEHAVIORAL

Step 3: Referral to Psychotherapist and/or Psychiatrist

Non-responders to previous treatment steps will be referred to an psychotherapist and/or psychiatrist for intensified treatment. Treatments procedures will be monitored and interventions will be scored to enable the evaluation of treatment effects.

Intervention Type BEHAVIORAL

Standard Diabetes Education

Standard diabetes education and professional care.

Includes:

* Health care and specific topics (e. g. blood pressure)
* Diabetes complications
* Healthy and unhealthy foods, cooking recommendations and recipes
* Foot care: exercises, care and control, injuries, and diabetic neuropathy
* Sports, activities and exercise
* Social aspects of living with diabetes

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age \>=18 and \<=70
* Diabetes mellitus
* Elevated depressive symptoms (CES-D score \>=16) and/or elevated diabetes-related distress (PAID score \>=40)
* Sufficient language skills (German)
* Written informed consent

Exclusion Criteria

* Severe depressive episode (F32.2/ F32.3)
* Current psychotherapeutic/ psychiatric treatment
* Current antidepressive medication
* Suicidal intention
* Current schizophrenia/ psychotic disorder, specified eating disorder, bipolar disorder, addictive disorder, personality disorder
* Severe physical illness (i.e. cancer, multiple sclerosis, dementia)
* Terminal illness
* Bedriddenness
* Guardianship
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

German Federal Ministry of Education and Research

OTHER_GOV

Sponsor Role collaborator

German Diabetes Center

OTHER

Sponsor Role collaborator

Heinrich-Heine University, Duesseldorf

OTHER

Sponsor Role collaborator

University of Giessen

OTHER

Sponsor Role collaborator

Helmholtz Zentrum München

INDUSTRY

Sponsor Role collaborator

Coordination Center for Clinical Trials (KKS)

UNKNOWN

Sponsor Role collaborator

Forschungsinstitut der Diabetes Akademie Mergentheim

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Norbert Hermanns

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Bernhard Kulzer, PD Dr.

Role: PRINCIPAL_INVESTIGATOR

Forschungsinstitut der Diabetes Akademie Mergentheim

Norbert Hermanns, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

Forschungsinstitut der Diabetes Akademie Mergentheim

Thomas Haak, Prof. Dr.

Role: STUDY_DIRECTOR

Forschungsinstitut der Diabetes Akademie Mergentheim

Johannes Kruse, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University of Giessen

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Forschungsinstitut der Diabetes Akademie Mergentheim e. V.

Bad Mergentheim, Baden-Wurttemberg, Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

References

Explore related publications, articles, or registry entries linked to this study.

Schmitt A, Kulzer B, Ehrmann D, Haak T, Hermanns N. Diabetes Distress and Depression during COVID-19: Response to Breznoscakova et al. Uncovering the Untold Emotional Toll of Living with Diabetes in the COVID-19 Era. Psychother Psychosom. 2022;91(4):288-289. doi: 10.1159/000524602. Epub 2022 May 6. No abstract available.

Reference Type BACKGROUND
PMID: 35526518 (View on PubMed)

Schmitt A, Kulzer B, Reimer A, Herder C, Roden M, Haak T, Hermanns N. Evaluation of a Stepped Care Approach to Manage Depression and Diabetes Distress in Patients with Type 1 Diabetes and Type 2 Diabetes: Results of a Randomized Controlled Trial (ECCE HOMO Study). Psychother Psychosom. 2022;91(2):107-122. doi: 10.1159/000520319. Epub 2021 Dec 7.

Reference Type RESULT
PMID: 34875666 (View on PubMed)

Herder C, Schmitt A, Budden F, Reimer A, Kulzer B, Roden M, Haak T, Hermanns N. Association between pro- and anti-inflammatory cytokines and depressive symptoms in patients with diabetes-potential differences by diabetes type and depression scores. Transl Psychiatry. 2018 Mar 9;7(11):1. doi: 10.1038/s41398-017-0009-2.

Reference Type RESULT
PMID: 29520075 (View on PubMed)

Herder C, Schmitt A, Budden F, Reimer A, Kulzer B, Roden M, Haak T, Hermanns N. Longitudinal associations between biomarkers of inflammation and changes in depressive symptoms in patients with type 1 and type 2 diabetes. Psychoneuroendocrinology. 2018 May;91:216-225. doi: 10.1016/j.psyneuen.2018.02.032. Epub 2018 Mar 6.

Reference Type RESULT
PMID: 29525039 (View on PubMed)

Schmitt A, Reimer A, Kulzer B, Haak T, Gahr A, Hermanns N. Assessment of diabetes acceptance can help identify patients with ineffective diabetes self-care and poor diabetes control. Diabet Med. 2014 Nov;31(11):1446-51. doi: 10.1111/dme.12553. Epub 2014 Aug 2.

Reference Type DERIVED
PMID: 25047992 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

FKZ 01GI1107

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Depression in Youth Onset Type 2 Diabetes
NCT06285487 NOT_YET_RECRUITING NA