Evaluation of the Organization of Continuity of Care for Home Hospice Patients by Four Parisian Health Networks
NCT ID: NCT03336489
Last Updated: 2018-12-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
200 participants
OBSERVATIONAL
2017-03-29
2018-11-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The study's goal is to compare patient's and caregiver's satisfaction between these two systems of continuity of care.
For that purpose, patients will be taken care of as usual by every palliative care network. In every instance where the patient or caregivers have reached out for medical help through the network's continuity of care system, the patient or caregiver will be called 5 days later by the investigation team to go through a satisfaction questionnaire (Likert scales)
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patient lives in Paris, France
* Patient benefits from home hospice care through one of the four official Paris palliative care networks
Exclusion Criteria
* Breastfeeding womed
* Altered cognitive function with a Mini Mental Status below 20
* Patient not able to communicate or not speaking French
* Patient legally not capable of giving informed consent
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fondation Ophtalmologique Adolphe de Rothschild
NETWORK
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Herve PICARD, MD MSc
Role: PRINCIPAL_INVESTIGATOR
Clinical Research Department, Rothschild Foundation, Paris (France)
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Reseau QUIETUDE
Paris, , France
Reseaux ROPE
Paris, , France
Reseau ENSEMBLE
Paris, , France
Reseaux ParisOuest
Paris, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
HPD_2016_24
Identifier Type: -
Identifier Source: org_study_id