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OpenTrials
Completed

NCT Number: NCT03336489

Evaluation of the Organization of Continuity of Care for Home Hospice Patients by Four Parisian Health Networks

In Paris, France, home hospice care for terminally ill patients is organized by four "palliative care networks". These networks are responsible for information sharing and coordination of all health care professionals working with the patient. Two different systems are in place to ensure continuity of care outside working hours, in such a setting. In the first system, palliative care specialists from the network are reachable over the phone 24/7 by the patient or its caregivers, whenever needed. In the second system, medical information about the patient, regularly updated by the network's medical team, is available to professionals via a secure website, so that in case the patient requires an urgent medical home visit outside working hours, the visiting physician has access to accurate information.

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)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Reseau ENSEMBLE, Paris, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient has a disease with fatal prognosis and requires palliative care
  • Patient lives in Paris, France
  • Patient benefits from home hospice care through one of the four official Paris palliative care networks

Exclusion criteria

  • Pregnant women
  • 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

Treatment and study plan

Primary outcomes

  1. Satisfaction about the response given by the network's continuity of care system

    Time frame: between the first and tenth day after the patient or caregiver activated the network's continuity of care system

    Patient's (or caregiver's) satisfaction about the response given by the network's continuity of care system, after the patient or caregiver activated this system at night time or during week-ends or bank holliday, as measured on a 4-level Likert scale (verbal questionnaire by phone call)

Sponsors and collaborators

Lead sponsor

Fondation Ophtalmologique Adolphe de Rothschild

Network

Registry information

Acronym: DICODOM

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Nov 8, 2017
Registry last updated
Dec 7, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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