MedPath

Online Training To Overcome Depressio

Not Applicable
Conditions
F32
Depressive episode
Registration Number
DRKS00005025
Lead Sponsor
euphana Universität LüneburgGET.ON Gesundheitstraining.Online / Innovations-Inkubator
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
131
Inclusion Criteria

access to Internet and e-mail
- diagnose of depressive episode (via SCID)

Exclusion Criteria

- acute psychotic symptoms (at baseline)
- current or former manic/hypomanic episode
- former diagnose of psychosis/schizophrenia
- suicide risk (score of BDI-II item 9 > 1)
- receiving psychotherapy
- changed medication against depression within 4 weeks before baseline

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of depressive symptoms (observer rated), measured with the Quick Inventory of Depressive Symptomatology (QIDS, Rush, 2003) and the Hamilton Rating Scale for Depression (HRSD, Hamilton, 1960/67) before treatment (baseline=pre) and after treatment (6 weeks=post)
Secondary Outcome Measures
NameTimeMethod
- course of depressive symptoms (Patient-Health-Questionnaire, PHQ-9): pre, post, follow up (12 weeks)<br>- activity level (Behavioural Activation Depression Scale, BA-DS, short version): pre, post, follow up<br>- anxiety symptoms (Hospital Anxiety and Depression Scale, HADS, anxiety subscale): pre, post, follow up<br>- problem solving (Social Problem Solving Inventory): pre, post, follow up<br>- attitudes towards seeking professional help (ATSPH-Scale): pre, post<br>- general health (Health Survey – Short Form, SF-12): pre, post, follow up<br>- well being (WHO Five Well-being Index): pre, post, follow-up<br>- side effects of psychotherapy (Inventar zur Erfassung negativer Effekte von Psychotherapie, INEP): post<br>- training satisfaction (Client Satisfaction Questionnaire, CSQ-8): post
© Copyright 2025. All Rights Reserved by MedPath