interprof HOME: Development and Testing of an Interprofessional, Person-centered Care Concept for People Living at Home With Care Needs.

Sponsor
University Medical Center Goettingen (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05149937
Collaborator
(none)
152
1
24.2

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: interprofessional, person-centered care concept
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
152 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Development and Testing of an Interprofessional, Person-centered Care Concept for People Living at Home With Care Needs.
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Jan 6, 2025
Anticipated Study Completion Date :
Jan 6, 2025

Arms and Interventions

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.

Other: interprofessional, person-centered care concept
interprofessional, person-centered care concept

Outcome Measures

Primary Outcome Measures

  1. cumulative number of hospitalisation [40 months]

    Cumulative incidence of hospitalisations within 40 months

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Medical Center Goettingen

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Karsten Gavenis, Clinical Study Management on behalf of the Principal Investigator, University Medical Center Goettingen
ClinicalTrials.gov Identifier:
NCT05149937
Other Study ID Numbers:
  • 2020-00425
First Posted:
Dec 8, 2021
Last Update Posted:
Jul 7, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Karsten Gavenis, Clinical Study Management on behalf of the Principal Investigator, University Medical Center Goettingen

Study Results

No Results Posted as of Jul 7, 2022