Viewing Study NCT02752295



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Last Modification Date: 2024-10-26 @ 12:01 PM
Study NCT ID: NCT02752295
Status: COMPLETED
Last Update Posted: 2016-09-16
First Post: 2016-04-07

Brief Title: Intensive Stress Coping Intervention Week - A Secondary Prevention For Real World Affective Disorder Patients
Sponsor: Medical University of Vienna
Organization: Medical University of Vienna

Study Overview

Official Title: Intensive Stress Coping Intervention Week - A Secondary Prevention For Real World Affective Disorder Patients
Status: COMPLETED
Status Verified Date: 2016-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ISCIW
Brief Summary: This study intents to determine who will benefit from an intensive brief stress coping intervention week ISCIW as secondary prevention for real world affective disorder patients
Detailed Description: Affective disorders are associated with a substantial personal and socio-economic burden This study evaluates an intensive brief stress-coping intervention week ISCIW as feasible follow-up treatment for real world patients who suffer from this highly prevalent and chronic stress-related disorders Stress-associated blood Interleukin-6 Homocystein Myeloperoxidase saliva cortisol and psychosocial screening parameters will be analyzed to determine who will benefit from the ISCIW All patients were identified in a preventive medical screening before pre-treatment for at least three month as outpatient and the following inclusion to the follow-up ISCIW-trial at the Health and Prevention Center Sanatorium Hera Vienna Austria For the three planed groups and interventions see interventions and arms

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None