- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05149937
Development and Testing of an Interprofessional, Person-centered Care Concept for People Living at Home With Care Needs. (interprof HOME)
The aim of the project is to develop and pilot measures to optimize the person-centered cooperation between nursing services, general practitioners and members of the therapeutic professions in the care of people living at home with care needs, so that hospital admissions and the use of unplanned medical and rescue services are avoided, the quality of life is improved and a deterioration in the need for long-term care can be stopped.
This is done by developing an interprofessional person-centered collaboration-concept, perform an explorative mixed-methods-study: interviews, focus groups, expert workshops, survey of best practices, shadowing, questionnaires.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Description of mixed-methods-study:
Interviews with
- 20 patients,
- 20 relatives,
- 5 experts of health insurance professionals,
- and 3 focus groups à 8 persons with general practioniers, nurses, therapists.
- investigation of best practice cases
explorative survey of 100 cases in each group:
- general practitioner
- nursing services
- therapists
- persons in need of care
- family members of persons in need of care
The mixed-methods-study is analysed in different ways:
- structured content analysis
- case-based qualitative analysis of interviews
- descriptive analysis
The mixed-methods-study has been approved by the ethics committee and is recruiting.
Study Type
Phase
- Not Applicable
Contacts and Locations
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- years of age >18
- receipt of benefits in the form of outpatient care according to SGB XI,
- preliminary / final classification of care ≥level 2
- expected life expectancy >6 months
- informed consent
- sufficient opportunity to answer answering questions about patient-reported outcomes
Exclusion Criteria:
- Living in nursing home / planned move-in within the following 6 months
- claim acceptance of SAPV
- participation in scientific study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Interventional group
Implementation of interprof Home measures to improve cooperation between nursing services, general practitioners and members of the therapeutic professions in the care of people living at home with care needs.
|
interprofessional, person-centered care concept
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
cumulative number of hospitalisation
Time Frame: 40 months
|
Cumulative incidence of hospitalisations within 12 months
|
40 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2020-00425
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.