access to services permitting the participation in professional life demand for services permitting the participation in professional life Z50
Conditions
Interventions
Group 1: Step 1.1: Analysis of routine data from DRV.
Step 1.2: Focus groups with rehab teams in rehab clinics
Step 1.3: Group discussions with institutions for vocational/occupational reintegration,
Sponsors
Medizinische Hochschule Brandenburg Theodor Fontane
Eligibility
Sex/Gender
All
Age
18 Years to 67 Years
Inclusion criteria
Inclusion criteria: Employees* (rehab clinics): At least 2 years of professional experience in the designated professional field and within the LMR facility (cooperation partner), Written consent for voluntary participation as well as knowledge + acceptance of the general, participant and privacy policy. Employees* (LTA facilities): At least 2 years of professional experience in their position or within the LTA facility (cooperation partner), Written consent for voluntary participation as well as knowledge and acceptance of the general, participant and privacy policy. Rehabilitants: Age of majority (18 years), Fulfillment of DRV criteria for medical rehabilitation (§26 SGB IX), Fulfillment of DRV criteria for vocational rehabilitation (§10 SGB VI)/LTA, general earning capacity, Participation in one of the measures of the cooperating institutions, Written consent for voluntary participation as well as knowledge + acceptance of the general, patient and data protection declaration. Relatives of rehabilitants: Direct relatives or co-affected persons from the direct vicinity of the rehabilitant, Social/emotional, immediate and significant involvement (e.g., co-support, support) in the case of illness relevant to rehabilitation (the relative has relevant knowledge about the findings, the course of the illness, the treatment and rehabilitation measures), Written consent to voluntary participation as well as acknowledgement and acceptance of the general, participant and data protection declaration.
Exclusion criteria
Exclusion criteria: No sufficient German language skills of the participants, Voluntary discontinuation of the study/withdrawal of consent (possible at any time and without any giving reasons), Medical, psychiatric or other conditions that limit the abilities of the rehabilitants/relatives/staff: to understand the participation information, to give informed consent, to adhere to the rules of protocol, or to complete the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Objectives: The target criteria will be determined in consultation with a project advisory board during the course of the study. Before the start of the pilot phase, the exact target criteria will be determined, on the basis of which the final evaluation (quantitative) will take place. The overall aim is to improve access to LTA and the transition process from medical to vocational/occupational rehabilitation for rehabilitants. | — |
Secondary
| Measure | Time frame |
|---|---|
| Objectives: In the course of the study, existing knowledge about possible improvements in the interface management between medical and vocational/occupational rehabilitation will be used, individual problems and needs/demands will be identified, targeted gaps in care will be closed through better networking, and low-threshold and target group-oriented access to LTA should be facilitated. | — |
Countries
Germany
Contacts
Public ContactPaulina Kuper
Medizinische Hochschule Brandenburg Theodor Fontane
Outcome results
None listed