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Clinical Trials/NCT03748225
NCT03748225
Completed
Not Applicable

The Fami-Life Study: Protocol of a Prospective Multicenter Observational Mixed Study of Psychological Consequences of Grieving Families in French Palliative Care Units on the Behalf of the F.R.I.P.C Research Network

Hôpital Franco-Britannique-Fondation Cognacq-Jay1 site in 1 country609 target enrollmentFebruary 4, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bereaved Families
Sponsor
Hôpital Franco-Britannique-Fondation Cognacq-Jay
Enrollment
609
Locations
1
Primary Endpoint
Risk factors of prolonged grief in bereaved family members
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to assess the incidence and risk factors of prolonged grief in family members of patients died in French palliative care units and to explore experience of bereaved families to build a scientifically valid management prevention program.

Detailed Description

There is hardly knowledge on how bereavement is treated in palliative care patient's relatives. The field of bereavement needs studies that validate the theoretical underpinning of the research area. This study will depict the grieving process of individuals having lost a relative in palliative care in France. Having baseline data of incidence of prolonged grief, risk factors of relative's prolonged grief and identification of risk factors associated with the management of end-of-life issues in palliative care will contribute to target interventions that should help decrease bereaved families burden. The investigator designed a quantitative study to assess the psychological effect of families after the death of the patient in palliative care unit and a qualitative study to examine the grieving prolonged process.

Registry
clinicaltrials.gov
Start Date
February 4, 2019
End Date
February 10, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Hôpital Franco-Britannique-Fondation Cognacq-Jay
Responsible Party
Principal Investigator
Principal Investigator

Maité Garrouste-Orgeas, MD

Director, head of clinical research, principal investigator, medical doctor

Hôpital Franco-Britannique-Fondation Cognacq-Jay

Eligibility Criteria

Inclusion Criteria

  • Families of adult patients hospitalized more than 72 hours in a palliative care unit for end-of-life care.
  • Eligibility of end-of-life cares are defined after the first evaluation by the palliative care physician.

Exclusion Criteria

  • Patients with less than 72 hours of life-expectancy
  • Patients or families who refused the study
  • Patients or families included in a study using the same questionnaires
  • Patients without families visiting them in the first 24 hours after admission
  • Patients not hospitalized for end-of-life issues
  • Families not fluent in French
  • Deaf or mute families

Outcomes

Primary Outcomes

Risk factors of prolonged grief in bereaved family members

Time Frame: 6 months after patient's death in palliative care unit

Hierarchical logistic regression models with a random effect center after selection of variables by univariate analysis then introduced in a multivariate analysis

Incidence of prolonged grief in bereaved family members

Time Frame: 6 months after patient's death in palliative care unit

Inventory Grief Disorder \> 25

Secondary Outcomes

  • Anxiety and depression symptoms in bereaved family members(6 months after patient's death in palliative care unit)
  • Post traumatic stress disorder in bereaved family members(6 months after patient's death in palliative care unit)
  • Anxiety and depression symptoms in family members(Between between day 3 and day 5 after patient admission in the palliative care unit)
  • Report of the families' grief experience in those who have signs of prolonged grief according to the Inventory of Complicated Grief questionnaire with a score > 25(Between 6 and 12 months after the patient' death.)

Study Sites (1)

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