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Family Psychoeducation for Major Depressive Disorder

Primary Purpose

Major Depressive Disorder

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Family psychoeducation
Social support group
Sponsored by
Mental Health Services in the Capital Region, Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Major Depressive Disorder focused on measuring Unipolar depression, Family Therapies, Psychoeducation, Family psychoeducation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Patients:

Inclusion Criteria:

  • Age between 18 and 75
  • Major depression diagnosis according to the ICD-10 established by a board certified psychiatrist and verified by the MINI International Neuropsychiatric Interview
  • Living together , or in very regular contact (every day or almost every day), with an adult relative that the patient considers as emotionally important and who are available for intervention

Regarding hypothesis 1 and 2, patients will be included if they are in remission or partial remission at the inclusion time defined as a score <13 on the Hamilton Rating Scale for Depression (HAM-D17) [20]. Patients included for the test of hypothesis 3 have a HAM-D17-score >13 at the time of the inclusion.

Exclusion Criteria:

  • Insufficient knowledge of Danish
  • Clinical suspicion of dementia
  • Alcohol, drug or medicine abuse
  • Psychotic symptoms
  • Co-morbidity of severe personality disorder
  • Having undergone ECT treatment during the index depressive episode
  • Maximum duration of the current depressive episode may not exceed 2 years
  • Maximum duration of a period with stable remission may not exceed 3 consecutive months

Regarding to the relatives following criteria for participation apply:

Inclusion criteria:

• Age between 18 and 75

Exclusion criteria:

• Insufficient knowledge of Danish

Sites / Locations

  • Psychiatric Research Unit, Mental Health Centre North ZealandRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Family psychoeducation

Social support group

Arm Description

The intervention consists of group-based family psychoeducation-program aimed at the patients' relatives. Each group will consist of 5 participants and the patients will not be present at group sessions. The program consists of four weekly sessions each consisting of both short lectures on relevant topics as well as interactive séances designed to give participants problem-solving skills.

Relatives in the social support group will attend the same number of sessions of the same duration, as the relatives in the intervention group (family psychoeducation). The psychiatric nurse who will be in charge of the social support group will not give any psychoeducational intervention.

Outcomes

Primary Outcome Measures

Number of relpase
The primary outcome is relapse defined as a score ≥ 7 on HAM-D6 [47] in the 9-month follow-up period (hypothesis 1) among remitted patients.

Secondary Outcome Measures

Time to relapse
The number of weeks from baseline to relapse, time to full remission defined as a HAM-D6 <5, among the partially remitted patients (hypothesis 2)
Reduction of depressive symptoms
Reduction of depressive symptoms in the HAM-D6-score (hypothesis 3).

Full Information

First Posted
January 5, 2015
Last Updated
April 27, 2016
Sponsor
Mental Health Services in the Capital Region, Denmark
Collaborators
Mental Health Centre North Zealand
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1. Study Identification

Unique Protocol Identification Number
NCT02348827
Brief Title
Family Psychoeducation for Major Depressive Disorder
Official Title
Family Psychoeducation for Major Depressive Disorder - a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2015 (undefined)
Primary Completion Date
July 2016 (Anticipated)
Study Completion Date
September 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mental Health Services in the Capital Region, Denmark
Collaborators
Mental Health Centre North Zealand

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the present study is to compare an intervention consisting of Family Psychoeducation (FPE) to an active control intervention of social support for relatives of patients with a diagnosis of major depression.
Detailed Description
More than 50 % of patients experiencing their first depressive episode will have at least one new episode. Therefore, effective interventions to reduce the risk of relapse are. Psychoeducation is an interactive education form enhancing knowledge about patients' illness, including it course, symptoms and treatment. Psychoeducational methods can also act as family intervention which already is an evidence-based practice in schizophrenia and bipolar disorder. In spite of unipolar depression's high prevalence, only few studies have focused on the effect of psychoeducation, including family psychoeducation, in the prevention of new depressive episodes. The aim of the present study is to compare an intervention consisting of Family Psychoeducation (FPE) to an active control intervention of social support for relatives of patients with a diagnosis of major depression. The following hypotheses are proposed: Psychoeducational intervention for relatives will reduces the risk of depressive relapse (defined as a score on The Hamilton six-item subscale, HAM-D6≥7), among remitted depressed patients compared to the control condition Psychoeducational intervention for relatives will shorten time to achieve full symptomatic remission (defined as a score HAM-D6<5) among partially remitted depressed patients compared to the control condition Psychoeducational intervention for relatives will more effectively reduce depressive symptoms (measured on the HAM-D6) among patients fully symptomatic currently depressed patients, compared to control condition. Secondary aims The study has as a secondary goal to investigate whether a high level of expressed emotion (EE) in relatives at baseline will be associated with poorer outcome, in the form of relapse, in depressed patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder
Keywords
Unipolar depression, Family Therapies, Psychoeducation, Family psychoeducation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Family psychoeducation
Arm Type
Experimental
Arm Description
The intervention consists of group-based family psychoeducation-program aimed at the patients' relatives. Each group will consist of 5 participants and the patients will not be present at group sessions. The program consists of four weekly sessions each consisting of both short lectures on relevant topics as well as interactive séances designed to give participants problem-solving skills.
Arm Title
Social support group
Arm Type
Active Comparator
Arm Description
Relatives in the social support group will attend the same number of sessions of the same duration, as the relatives in the intervention group (family psychoeducation). The psychiatric nurse who will be in charge of the social support group will not give any psychoeducational intervention.
Intervention Type
Behavioral
Intervention Name(s)
Family psychoeducation
Intervention Type
Behavioral
Intervention Name(s)
Social support group
Primary Outcome Measure Information:
Title
Number of relpase
Description
The primary outcome is relapse defined as a score ≥ 7 on HAM-D6 [47] in the 9-month follow-up period (hypothesis 1) among remitted patients.
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Time to relapse
Description
The number of weeks from baseline to relapse, time to full remission defined as a HAM-D6 <5, among the partially remitted patients (hypothesis 2)
Time Frame
Up to 9 months from baseline
Title
Reduction of depressive symptoms
Description
Reduction of depressive symptoms in the HAM-D6-score (hypothesis 3).
Time Frame
9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Patients: Inclusion Criteria: Age between 18 and 75 Major depression diagnosis according to the ICD-10 established by a board certified psychiatrist and verified by the MINI International Neuropsychiatric Interview Living together , or in very regular contact (every day or almost every day), with an adult relative that the patient considers as emotionally important and who are available for intervention Regarding hypothesis 1 and 2, patients will be included if they are in remission or partial remission at the inclusion time defined as a score <13 on the Hamilton Rating Scale for Depression (HAM-D17) [20]. Patients included for the test of hypothesis 3 have a HAM-D17-score >13 at the time of the inclusion. Exclusion Criteria: Insufficient knowledge of Danish Clinical suspicion of dementia Alcohol, drug or medicine abuse Psychotic symptoms Co-morbidity of severe personality disorder Having undergone ECT treatment during the index depressive episode Maximum duration of the current depressive episode may not exceed 2 years Maximum duration of a period with stable remission may not exceed 3 consecutive months Regarding to the relatives following criteria for participation apply: Inclusion criteria: • Age between 18 and 75 Exclusion criteria: • Insufficient knowledge of Danish
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nina Timmerby, MD
Phone
+4538643197
Email
nina.02.timmerby@regionh.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nina Timmerby Timmerby, MD
Organizational Affiliation
Mental Health Centre North Zealand, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Psychiatric Research Unit, Mental Health Centre North Zealand
City
Hilleroed
ZIP/Postal Code
3400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nina Timmerby, MD
Phone
+4538643197
Email
nina.02.timmerby@regionh.dk

12. IPD Sharing Statement

Citations:
PubMed Identifier
27577267
Citation
Timmerby N, Austin SF, Ussing K, Bech P, Csillag C. Family psychoeducation for major depressive disorder - study protocol for a randomized controlled trial. Trials. 2016 Aug 30;17(1):427. doi: 10.1186/s13063-016-1549-0.
Results Reference
derived
Links:
URL
https://www.psykiatri-regionh.dk/forskning/For-patienter/Sider/psykoedukation_depression.aspx
Description
For information about the project (in Danish)

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Family Psychoeducation for Major Depressive Disorder

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