Health-related, self-reported outcomes such as well-being, depressive symptoms, anxiety symptoms, and caregiver burden in the home setting assessed by pre-post survey.
Conditions
Interventions
Group 1: The primary objective of the exploratory observational study is to examine the health effects of a stay at the PflegeÜbungsZentrum of Caritas in Mellrichstadt (Subproject 1) or at the PflegeÜ
Sponsors
Institut für Klinische Epidemiologie und Biometrie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Included will be informal and related caregivers as well as people in need of care who complete a stay at the Care Training Center (Subproject 1) or the Care Training Mobile Home (Subproject 2).
Exclusion criteria
Exclusion criteria: None.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints for the group of family caregivers in subproject 1 and subproject 2 are: a) Well-being, measured using the WHO-5 Well-Being Index (WHO-5) b) Anxiety symptoms, measured using the Patient Health Questionnaire-4 (PHQ-4) c) Depressive symptoms, measured using the Patient Health Questionnaire-4 (PHQ-4) d) Burden among caregivers or caring persons, measured using the Home Care Scale (Häusliche Pflege-Skala, HPS) The primary endpoints for people in need of care in subproject 1 and subproject 2 are: a) Well-being, measured using the WHO-5 Well-Being Index (WHO-5) | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoints in subproject 1 and subproject 2 include: a) The health status of the family caregiver b) The health status of the person in need of care c) The home care situation from the perspective of the family caregiver d) The home care situation from the perspective of the person in need of care | — |
Countries
Germany
Contacts
Public ContactThomas Keil
Institut für Klinische Epidemiologie und Biometrie
Outcome results
None listed