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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03217864
Other study ID # 6843
Secondary ID
Status Recruiting
Phase N/A
First received July 11, 2017
Last updated July 13, 2017
Start date July 12, 2017
Est. completion date July 2018

Study information

Verified date July 2017
Source University Hospital, Strasbourg, France
Contact Laurent CALVEL, MD, PhD
Phone 33 3 88 12 83 39
Email laurent.calvel@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hospitalization at home is booming. It is designed to meet the demands of patients and their families to continue care at home. It partially solves the problem of the lack of places in the "long-term care" structures and allows to respond to a desire of the health policy to reduce the lengths of stay in the hospital. Hospitalization at home is also an alternative in the management of chronic patients. Nevertheless, at the moment a certain number of requests for hospitalization at home remain unsuccessful or their implementation is complicated. In addition, the number of home health care provider has increased significantly in recent years. According to the federation of home health care provider, the number of beneficiaries increased by 1.7% in 4 years. The home health care provider would support 1,200,000 patients per year.

The objective of the study is to analyze the factors participating in Implementation of a return home with a Hospitalization at home or a home health care provider during a return home project constructed with the patient and his / her relatives from the services of Oncology, oncology, hematology of the University Hospital of Strasbourg.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date July 2018
Est. primary completion date July 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient over 18 years old

- Patient for whom an application for Hospitalization at home or with a home health provider is initiated by the Oncology, Oncology or Hematology Department of the University Hospital of Strasbourg.

Exclusion Criteria:

- Refusal to participate in the study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service Soins Palliatifs Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analysis of factors participating in Implementation of a return home with a Hospitalization at home or a home health care provider 15 days after patient discharge from hospital
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