Comprehensive Study of Social Representation of Platelet Transfusion in Patients Followed for Advanced Hematological Malignancies (R-PLQ)

Sponsor
Centre Hospitalier Universitaire de Besancon (Other)
Overall Status
Completed
CT.gov ID
NCT03806712
Collaborator
(none)
45
1
3.7
12.2

Study Details

Study Description

Brief Summary

Limited data is available for end of life care in hematologic malignancies, moreover with thrombocytopenic patients. Thrombopenia is a frequent complication, specific of bone marrow involvement in those diseases or its treatments. Yet, a few studies was interested in, whereas platelet transfusion is the only treatment indicated. As it represent a scarce, limited resource, the ethical principles are in conflict in this setting and there's a lack of recommendation. The final decision is take by the clinician and his patient, but no study exist in representation of the two parts. We provide a qualitative study to understand what this decision is made of.

Condition or Disease Intervention/Treatment Phase
  • Other: multi method questionary (developped by De Rosa, in 1995 and 2014)

Study Design

Study Type:
Observational
Actual Enrollment :
45 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Comprehensive Study of Social Representation of Platelet Transfusion in Patients Followed for Advanced Hematological Malignancies (R-PLQ)
Actual Study Start Date :
Apr 1, 2019
Actual Primary Completion Date :
Jun 1, 2019
Actual Study Completion Date :
Jul 22, 2019

Arms and Interventions

Arm Intervention/Treatment
patient

patient with advanced, non curative hematological malignancies multi method questionary, at least 1 hour per patient

Other: multi method questionary (developped by De Rosa, in 1995 and 2014)
questions from an association network according to the subject and the grounded theorise (Glasser and Strauss)

hematologist

medical practitioner of platelet transfusion multi method questionary, at least 1 hour per hematologist

Other: multi method questionary (developped by De Rosa, in 1995 and 2014)
questions from an association network according to the subject and the grounded theorise (Glasser and Strauss)

Nurses

nurses working in hematology, practicing platelet transfusion multi method questionary, at least 1 hour per nurse

Other: multi method questionary (developped by De Rosa, in 1995 and 2014)
questions from an association network according to the subject and the grounded theorise (Glasser and Strauss)

Outcome Measures

Primary Outcome Measures

  1. measure the impact of social representation on platelet transfusion practice [3 months]

    inner core and peripheral items of platelet transfusion of each participant will be collected until reaching saturation, it's to say that the repetition of some terms will be measured between each interview thank's to a questionnaire of at least two principals opened questions.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • major patient

  • patient with advanced hematological malignancies

  • patient transfused in platelet regularly (3 time at least in last month)

  • medical practioner, hematologist, prescribing platelet transfusion at least one per week.

  • nurse working in hematology, practicing platelet transfusion at lest one peer week.

Exclusion Criteria:
  • minor patient

  • non communicant patient

  • non transfused platelet patient

  • non voluntary patient or hematologist or nurses

  • non graduated hematologist

Contacts and Locations

Locations

Site City State Country Postal Code
1 Moracchini Besançon France 25000

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Besancon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Centre Hospitalier Universitaire de Besancon
ClinicalTrials.gov Identifier:
NCT03806712
Other Study ID Numbers:
  • P/2019/413
First Posted:
Jan 16, 2019
Last Update Posted:
Jul 25, 2019
Last Verified:
Jul 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre Hospitalier Universitaire de Besancon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 25, 2019