Evaluation of the primary prevention program Lebe Balance

Not Applicable

• Conditions: Z73; Problems related to life-management difficulty

• Registration Number: DRKS00006216
• Lead Sponsor: AOK Baden-Württemberg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-06-11
• Study Completion: 2015-11-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 3626

Inclusion Criteria

Participants of the prevention courses; matched controls (age, gender, health costs)

Exclusion Criteria

Insufficient comprehension of the German language, impaired ability to judge or capacity to consent.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Measurement time points are previous to participation in the course (t0), after completing the course (t1= t0+10 weeks) and 3 months follow-up (t2 = t1 + 12 weaks).<br>This study is carried out with questionnaire-based self-ratings. The following measures are used at all three time points. <br>• „Satisfaction with Life Scale (SWLS; Glaesmer et al., 2011)<br>• Resilience Scale (11 Item-Version) von Wagnild und Young (Wagnild et al., 1993, dt. von Schumacher, Leppert, Gunzelmann, Strauß & Brähler, 2005)<br>• „Hospital Anxiety and Depression Scale (HADS-D; Herrmann, Buss & Snaith, 2007)<br>The specific and unspecific health costs are drawn from the insurance company’s stock data.<br>

Secondary Outcome Measures

Name	Time	Method
Secondary criteria are compliance, course satisfaction and lasting behavior changes in the study-group. These criteria are measured at t1 and t2 (maintaining of behavior change) via self-developed items.