Effects of a supportive German online program for people with depression or adjustment: A randomized controlled trial

Not Applicable

Recruiting

• Conditions: F32.0; F32.1; F33.0; F33.1; F34.1; F43.2; Mild depressive episode; Moderate depressive episode; Recurrent depressive disorder, current episode mild; Recurrent depressive disorder, current episode moderate

• Registration Number: DRKS00004616
• Lead Sponsor: euphana Universität LüneburgInnovations-InkubatorKompetenztandem Vernetzte Versorgung

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-01-07
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 608

Inclusion Criteria

F32.0; F32.1; F33.0; F33.1; F34.1; F43.2;
Current incapacity to work certificate;
Internet access/e-mail account

Exclusion Criteria

Presence of severe depression;
Risk of suicide (dedicated collection of active and passive suicidal tendencies);
Missing declaration of consent (informed consent)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Improvement of depressive symptoms or symptoms of adjustment disorder (weekly screening by the PHQ-9; pre-post measurement with two follow-ups by the BDI-II)

Secondary Outcome Measures

Name	Time	Method
Reduction of sick days (routine data analysis) and positive effects on patient reported outcomes (PROs; including quality of life, self-efficacy, physical and mental stress symptoms measured by EQ-5D, MANSA, ASF, SCL-14) and the use of disease-related services covered by the German statutory health insurance (SHI) (e.g. prescriptions, doctor consultations and hospitalization from routine data analysis).