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Comparison of Lower-risk MDS Patients With and Without Improvements in Fatigue Following Blood Transfusion Therapy (FITME)

Primary Purpose

Myelodysplatic Syndromes

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Physiological tests to measure fatigue level
Sponsored by
Centre Hospitalier Universitaire de Saint Etienne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Myelodysplatic Syndromes focused on measuring Myelodysplatic syndromes, elderly, fatigue, blood transfusion, physiopathology

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient affiliated to a social security regimen or beneficiary of the same
  • Signed written informed consent form
  • Patient, ≥ 18 years-old, with established diagnosis of myelodysplastic syndrome with low or intermediate-1 risk cytogenetic profile
  • FACIT-F score ≤ 34,
  • Indication of blood transfusion.

Exclusion Criteria:

  • Contra-indication to experimental procedures and/or physical exercise,
  • Concomitant cancer diagnosis,
  • Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent
  • Refusing participation.

Sites / Locations

  • CHU de Saint-Etienne

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MDS patients

Arm Description

MDS patients receiving blood transfusion

Outcomes

Primary Outcome Measures

Measurement of Fatigue using FACIT-F questionnaire
Measurement of Fatigue will be performed using FACIT-F questionnaire. This is a questionnaire with 13 questions about which the patient is positioned on a Likert scale ranging from 1 to 5 (1 = quite, 5 = not at all). By adding the answers, a score out of 65 is obtained. Unlike other scales the higher the score the less the patient is tired. As an indication, the non-sick average positions is 40.1 on this scale.

Secondary Outcome Measures

Full Information

First Posted
September 24, 2019
Last Updated
May 4, 2023
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Laboratoire Interuniversitaire de Biologie de la Motricité - Jean Monnet University Saint-Etienne, Institut de Cancérologie de la Loire
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1. Study Identification

Unique Protocol Identification Number
NCT04103359
Brief Title
Comparison of Lower-risk MDS Patients With and Without Improvements in Fatigue Following Blood Transfusion Therapy
Acronym
FITME
Official Title
Fatigue in Myelodysplasic Patients : Why Blood Transfusion Does Not Systematically Improve Symptoms? (FITME Study)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Terminated
Why Stopped
inclusion rate too low
Study Start Date
October 20, 2020 (Actual)
Primary Completion Date
October 20, 2020 (Actual)
Study Completion Date
October 20, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Laboratoire Interuniversitaire de Biologie de la Motricité - Jean Monnet University Saint-Etienne, Institut de Cancérologie de la Loire

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
At present, it is unclear why some myelodysplastic patients (MDS) receiving blood transfusion therapy exhibit an increase in Hemoglobin (Hb) without a concurrent improvement in fatigue. Research is thus required to elucidate on why fatigue persists in some MDS patients in order to devise strategies to alleviate fatigue in "non-responders" to blood transfusion.
Detailed Description
One hypothesis is that patients who exhibited persistent fatigue following a blood- transfusion- induced increase in Hb have an impaired ability to utilize oxygen at the peripheral level. This could be the consequence of impairments in vascular function, mediated by endothelial dysfunction as a result of transfusion-induced iron-overload and oxidative stress associated with the disease. Taking the current gaps in knowledge pertaining to MDS-related fatigue into account, the objective of this study is to improve understanding on the aetiology fatigue in MDS patients. To achieve this aim, the study will measure a comprehensive group of patient-reported and disease-related outcomes: i) prior to blood transfusion therapy when Hb levels are low and; ii) following blood transfusion therapy, when Hb levels have been increased. Results from the post-transfusion tests will be analyzed to determine which participants remain fatigued despite an increase in Hb, and which participants shown an improvement in fatigue.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myelodysplatic Syndromes
Keywords
Myelodysplatic syndromes, elderly, fatigue, blood transfusion, physiopathology

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MDS patients
Arm Type
Experimental
Arm Description
MDS patients receiving blood transfusion
Intervention Type
Other
Intervention Name(s)
Physiological tests to measure fatigue level
Intervention Description
Physiological tests to measure fatigue level
Primary Outcome Measure Information:
Title
Measurement of Fatigue using FACIT-F questionnaire
Description
Measurement of Fatigue will be performed using FACIT-F questionnaire. This is a questionnaire with 13 questions about which the patient is positioned on a Likert scale ranging from 1 to 5 (1 = quite, 5 = not at all). By adding the answers, a score out of 65 is obtained. Unlike other scales the higher the score the less the patient is tired. As an indication, the non-sick average positions is 40.1 on this scale.
Time Frame
10 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient affiliated to a social security regimen or beneficiary of the same Signed written informed consent form Patient, ≥ 18 years-old, with established diagnosis of myelodysplastic syndrome with low or intermediate-1 risk cytogenetic profile FACIT-F score ≤ 34, Indication of blood transfusion. Exclusion Criteria: Contra-indication to experimental procedures and/or physical exercise, Concomitant cancer diagnosis, Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent Refusing participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Denis Guyotat, PhD
Organizational Affiliation
CHU de Saint-Etienne
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Saint-Etienne
City
Saint-Étienne
ZIP/Postal Code
42055
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparison of Lower-risk MDS Patients With and Without Improvements in Fatigue Following Blood Transfusion Therapy

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