MedTrace Logo

Intensive Stress Coping Intervention Week - A Secondary Prevention For Real World Affective Disorder Patients

NCT02752295 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 43

Last updated 2016-09-16

No results posted yet for this study

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.

Conditions

  • Affective Disorders
  • Psychological Stress
  • Inflammation
  • Oxidative Stress
  • Anxiety Disorders
  • Mood Disorders
  • Emotions

Interventions

BEHAVIORAL

stress-coping week

The multidisciplinary team will offer Mindfulness-Based Stress Reduction (MBSR), group psychotherapy (resilience, Cognitive Behavioral Analysis System of Psychotherapy CBASP, psychodynamic therapy), relaxation training, nutrition course, stress-coping and physical training in a group setting.

BEHAVIORAL

additional two days follow-up weekend

A two-days follow-up which recapitulates previous treatment elements.

Sponsors & Collaborators

  • Sanatorium Hera Vienna

    collaborator UNKNOWN

  • Medical University of Vienna

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2016-07-31
Completion
2016-07-31

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02752295 on ClinicalTrials.gov