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Wabe-Net: Overcoming unemployment through networked needs assessment and service provision - A cooperative joint project in Rhineland-Palatinate and Saarland

Wabe-Net: Overcoming unemployment through networked needs assessment and service provision - A cooperative joint project in Rhineland-Palatinate and Saarland - Wabe-Net

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00023037
Enrollment
1100
Registered
2020-09-28
Start date
2020-10-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The intervention is available to all job-seekers who meet the inclusion criteria, regardless to their specific diagnosis.

Interventions

Group 1: Intervention group: extended catalog of services and networking of DRV and AA/JC consultants. Group 2: control group: current catalog of measures of the DRV or AA/JC.

Sponsors

Universitätsklinikum Freiburg Institut für Medizinische Biometrie und Statistik Sektion Versorgungsforschung und Rehabilitationsforschung
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Voluntary project participation - At least one other obstacle to placement (besides the disability) - Rehabilitant* in the DRV Rhineland-Palatinate /DRV Saarland - Customer*at the employment agencies (AA) or job centers (JC) involved in the project or persons threatened by unemployment - Existing prohibition of services

Exclusion criteria

Exclusion criteria: - Rehabilitant*in need of at least 24 months of further training (qualification, retraining) - Participants*in ongoing retraining and the subsequent 6-month graduate management - Lack of motivation - Existing participation in another rehapro model project

Design outcomes

Primary

MeasureTime frame
The reintegration of the unemployed rehabilitants into working life. This criterion is considered to be fulfilled if the person undergoing rehabilitation is in employment 6 months after the end of the measure. The aim is to improve reintegration by 17%. In addition, it is examined whether the insured persons in the intervention group are in employment for a longer period of time than the control group at the end of the intervention and 6 months after the end of the intervention, and whether they were able to be integrated into working life earlier.

Secondary

MeasureTime frame
(1) the change in barriers to mediation over the course of the intervention (2) the cost-benefit ratio (3) the satisfaction of the rehabilitants with the model project and its elements (4) the acceptance of the rehabilitants and counselors towards the cross-sectoral counseling offer and the resulting reintegration plan

Countries

Germany

Contacts

Public ContactFranziska;Lena Kessemeier;Staab

Universitätsklinikum Freiburg Institut für medizinische Biometrie und Statistik Sektion Versorgungsforschung und Rehabilitationsforschung (SEVERA);Universitätsklinikum Freiburg Institut für medizinische Biometrie und Statistik Sektion Versorgungsforschung und Rehabilitationsforschung (SEVERA)

franziska.kessemeier@uniklinik-freiburg.de;lena.staab@uniklinik-freiburg.de+49 761 270-73530;+49 0761/270-74292

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026