Skip to main content
OpenTrials
Completed

NCT Number: NCT06053918

Research-Action in Hematology From Hospitalization to Home

Objective :

To study and support the hospitalization and the return home of patients with the help of a psychological follow-up started in a hospital institution and which will continue in the patient's home, based on the concepts of transitionality and narrativity.

Material and method To do this, the subjects will benefit from psychological interviews where they will freely discuss what concerns them, whether it is illness, treatment, returning home, or any other personal subject.

They will be divided into two groups of 5 patients each, one of the groups will benefit from follow-up in an institution as contracted for several years between the Institute of Hematology and the psychologists of the UMDSP, another from the same follow-up but with the presence of the psychologist at the time of discharge extended to the patient's home after leaving the hospital for a period of 2 months.

To ensure a certain consistency in the evaluation criteria, these will be standardized in the form of questionnaires completed blindly by the patient, a caregiver and the investigator, at 3 key times of the research (entry, discharge from hospital, two months after this discharge)

Device tested:

The aim of this work is to test the benefits of a device based on transitionality, which can limit, thanks to the restoration of the symbolization process, the deleterious effects of each of the stages imposed by the disease, the care and the resumption of autonomy once the active phase of care has passed.

Narrativity is also at the heart of this transitional device. It makes it possible to evoke the present experience of the patient in connection with future projects and in the continuity of past, potentially traumatic events. It opens onto a dynamic temporal perspective where the trauma freezes.

The whole process promotes the subjective reappropriation of the experience and a psychic well-being.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CAEN University Hospital

Caen, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patient hospitalized Protected Hematology Unit
  • patient with haematologic cancer
  • patient requesting psychological assistance or accepting proposed psychological assistance
  • signed informed consent

Exclusion criteria

  • patient refusing to participate
  • patient not able to participate

Treatment and study plan

additional follow-up extension at home

Other

additional interview when leaving the sector, and the extension of follow-up of the patient at home

Primary outcomes

  1. Clinical evaluation of the psychological state, anxiety-depressive disorders

    Time frame: At hospital Month 0 and at home Month 2

    anxiety-depressive disorders yes or no

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Registry information

Official study title

Psychological Follow-up in a Protected Hematology Unit as a Transitional Device Between Hospitalization and Return Home

Acronym: RAH HD

Important dates

Study start
2019
Primary completion
2020
Study completion
2021
First posted
Sep 26, 2023
Registry last updated
Sep 26, 2023

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.

Published trials that share one or more normalized conditions with this study.