Depressive reactionto traumatic experiences and its impact on mother-child interactio

Not Applicable

Recruiting

• Conditions: F32; Z61; Depressive episode; Problems related to negative life events in childhood

• Registration Number: DRKS00004231
• Lead Sponsor: Psychiatrische Universitätsklinik der Charité, St. Hedwig Krankenhaus

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-01-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 168

Inclusion Criteria

Depression & Trauma Group:
Age of mother > 17;
Experience of abuse in childhood;
At least one depressive episode in the past;
Depression remitted;
Medication stable for 2 weeks;
Age of child: 5-11 years;
Mother and child live together;
Sufficient knowledge of German

Group depression without trauma:
Age of mother > 17;
At least one depressive episode in the past;
Depression remitted;
Medication stable for 2 weeks;
Age of child: 5-11 years;
Mother and child live together;
Sufficient knowledge of German

Control group
Age of mother > 17;
Age of child: 5-11 years;
Mother and child live together;
Sufficient knowledge of German

Exclusion Criteria

Trauma & Depression Group
Acute suicidal tendency
Schizophrenic or schizoaffective disorder, mania, bipolar disorder, borderline personality disorder, antisocial personality disorder, dementia, substance-related addiction in the last six months (exception nicotine), benzodiacepine medication
Mental retardation or physical disability of mother or child,
Danger to child welfare;
Organic Diseases of mother or child interfering with study-related assessment.

Depression without trauma Group
Acute suicidal tendency
Experience of abuse in childhood
Schizophrenic or schizoaffective disorder, mania, bipolar disorder, borderline personality disorder, antisocial personality disorder, dementia, substance-related addiction in the last six months (exception nicotine), benzodiacepine medication
Mental retardation or physical disability of mother or child,
Danger to child welfare;
Organic Diseases of mother or child interfering with study-related assessment.

Control group
Past or present psychiatric disorder
Acute suicidal tendency
Experience of abuse in childhood
Schizophrenic or schizoaffective disorder, mania, bipolar disorder, borderline personality disorder, antisocial personality disorder, dementia, substance-related addiction in the last six months (exception nicotine), benzodiacepine medication
Mental retardation or physical disability of mother or child,
Danger to child welfare;
Organic Diseases of mother or child interfering with study-related assessment.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Maternal Outcome:<br>Maternal sensitivity (Emotional Availability Scales): Difference between Baseline and Follow-Up-1 (Measurement after intervention).<br>Child Outcome: <br>Child Life Quality (KidScreen): Difference between Baseline and Follow-Up-1 (Measurement after intervention).