NCT03996174

Brief Summary

This qualitative study aims to explore the assessment of palliative care needs of the population living in Mayotte, French territory of the Comoros. The aim is to offer a palliative care service tailored to the needs of the population in this area.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Sep 2018

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2018

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

June 3, 2019

Completed
21 days until next milestone

First Posted

Study publicly available on registry

June 24, 2019

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 28, 2019

Completed
1.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

May 18, 2021

Completed
Last Updated

July 9, 2021

Status Verified

May 1, 2021

Enrollment Period

10 months

First QC Date

June 3, 2019

Last Update Submit

July 8, 2021

Conditions

Palliative Therapy

Keywords

Palliative careneeds assessmentMayotteterminal care

Outcome Measures

Primary Outcomes (1)

  • individual semi-structured interviews

    individual semi-structured interviews to obtain a aata saturation Reliability and Validity of the research described according to Guba.

    day 1

Interventions

InterviewOTHER

Interview bases on the use of an interview guide, during one hour maximum

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

3 studies will be conducted: one with "palliative patients" identified by their care workers, one with their family or caregivers, and one with their care workers. .

You may qualify if:

  • patients study: to be at the palliative stage of his illness, informed consent
  • family study: being a family or caregiver of a patient in palliative care, informed consent
  • care workers study: being a care worker of a patient in palliative care, informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHRU Besançon

Besançon, 25000, France

Location

MeSH Terms

Interventions

Interviews as Topic

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Régis Aubry, MD, PhD

    Service douleur, soins palliatifs

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 3, 2019

First Posted

June 24, 2019

Study Start

September 1, 2018

Primary Completion

June 28, 2019

Study Completion

May 18, 2021

Last Updated

July 9, 2021

Record last verified: 2021-05

Locations

FR(1)