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Prevention of Vasovagal Reactions in First-time Blood Donors Using a Combined PSYchological and Physiological Approach (PREDONPSY)

Primary Purpose

Vasovagal Reaction

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Psychological strategy
Physiological strategy
Sponsored by
Hospices Civils de Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Vasovagal Reaction focused on measuring first time donor, whole blood donation, vasovagal Reaction, physiological, psychological, BDRI, BDAS

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: M/F between 18 and 70 years old, A first-time donor who wishes to donate blood in Lyon, either at a fixed site or at a mobile unit, Declared fit to donate whole blood after the EFS pre-donation interview, Weight ≥ 50kg and height ≥ 135 cm, Available for telephone contact between to 5d +/- 2 days after donation, Having signed a written consent to participate in the study. Non-inclusion criteria: Known allergy to shellfish, and/or gluten, and/or milk, and/or soy, Incomprehension of the French language, First-time donor under protective measures (guardian, curator) or any other administrative measure, Not affiliated to the French social security system or any other equivalent system, Pregnant or breastfeeding woman, Subject participating in any other interventional or non-interventional research Exclusion Criteria: Withdrawal of consent First-time donor with anemia following routine hemoglobin testing First-time donor not reachable for telephone interview

Sites / Locations

  • French Blood Establishment (EFS)

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

No Intervention

Experimental

Experimental

Experimental

Arm Label

Control group

Test Group 1

Test Group 2

Test group 3

Arm Description

EFS usual standard practices for the whole blood donation

A psychological strategy is added to EFS standard practices before the whole blood donation flyer given at the interview presenting the 4 most frequent fears as well as a description of the recommended muscular and breathing exercises, followed by a training of these exercises and their execution

A physiological strategy is added to EFS standard practices before the whole blood donation : - Ingesting a salty snack.

The both psychological and physiological strategies are added to EFS standard practices before the whole blood donation flyer given at the interview presenting the 4 most frequent fears as well as a description of the recommended muscular and breathing exercises, followed by a training of these exercises and their execution Ingesting a salty snack.

Outcomes

Primary Outcome Measures

Vasovagal reactions (VVR)
Proportion of first-time donors experiencing VVR (immediate and delayed up to 48 hours) during whole blood donation managed by both psychological and physiological strategies (group 4) compared to usual standard practices (group 1)

Secondary Outcome Measures

VVR psychological strategy
Proportion of first-time donors experiencing VVR (immediate and delayed up to 48 hours) during whole blood donation managed by psychological strategy (group 2) compared to usual standard practices (group 1)
VVR physiological strategy
Proportion of first-time donors experiencing VVR (immediate and delayed up to 48 hours) during whole blood donation managed by physiological strategy (group 3) compared to usual standard practices (group 1)
Immediate VVR
Proportion of first-time donors with immediate VVR compared between the groups
Delayed VVR
Proportion of first-time donors with delayed VVR compared between the groups
First-time donor adherence
Adherence of the primary donor to the study strategies and to the EFS recommendations (complete intake of salty snacks, hydration, performance of muscle and breathing exercises training, performance of muscle and breathing exercises during donation, compliance with the duration of post-donation monitoring stage).
Anxiety/fear
Assessment of the evolution of the "anxiety/fear" score between arrival and before the whole blood donation, compared between the groups. This questionnaire consists of the 6-item Blood Donor Anxiety Scale (BDAS) (5-point Likert scale) (Chell et al., 2016) and a 4-item component with a 5-point Likert scale that allows for an assessment of the 4 most common donor fears (of the needle, to see blood, to feel pain, to experience sensations of discomfort). The scoring is obtained by summing up the responses to the different items. Score is between 10 and 50, a higher score is associated to a better outcome.
Sense of control and fears
Assessment of the "sense of control and fears" score, compared between the groups. The concepts measured here are the feeling of control related to giving blood (5 items) and the feeling of control over fears (4 items) according to a 5-point Likert scale. The scoring is obtained by summing up the answers to the different items. Score is between 9 and 45, a higher score is associated to a better outcome.
Feelings of discomfort
Assessment of the "feelings of discomfort" score, compared between the groups. The BDRI (Blood Donation Reactions Inventory) (France et al., 2008) provides an assessment of the subjective evaluation of 11 pre-syncopal symptoms (5-point Likert scale). The BDRI is easily understood by donors and is rapid. The BDRI provides important information about the donor experience to predict satisfaction and likelihood of re-donation. The score is calculated by summing up the responses to the various items. Score is between 11 and 55, a higher score is associated to a worse outcome.
First-time donor retention
Compared between the groups the number of first-time donors who made a second blood donation in the 12 months following the first-time donation, collected by query from the EFS computerized file

Full Information

First Posted
August 21, 2023
Last Updated
October 2, 2023
Sponsor
Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT06014346
Brief Title
Prevention of Vasovagal Reactions in First-time Blood Donors Using a Combined PSYchological and Physiological Approach
Acronym
PREDONPSY
Official Title
Prospective Study of the Prevention of Vasovagal Reactions in First-time Whole Blood Donors Using a Combined PSYchological and Physiological Approach: PREDONPSY
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 10, 2023 (Anticipated)
Primary Completion Date
May 18, 2025 (Anticipated)
Study Completion Date
August 18, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon

4. Oversight

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

5. Study Description

Brief Summary
The prevention of vasovagal reactions (VVR) occurring during or after donation is a major issue for the French Blood Establishment (EFS), firstly to guarantee the safety of donors but also to retain them, as this reaction is one of the negative experiences affecting the return to donation. The EVASION study conducted in the Auvergne Rhône-Alpes region (AURA) on 4828 donors representative of the French donor population, reported a beneficial effect of muscle contraction exercises to prevent the occurrence of VVR during donation, while hydric solutions, and even more so isotonic solutions, were likely to decrease the frequency of delayed VVR. These preventive measures have been integrated into the internal guidelines and currently include muscular and breathing exercises and hydration. Nevertheless, the isotonic solution could not be routinely deployed for feasibility and cost reasons. A salty snack could replace the isotonic solution to produce the same effects with better feasibility and acceptability. Furthermore, a significant proportion of discomfort is psychological in origin, related to stress and anxiety which persist despite these measures, particularly in the first-time donor population. These measures, which are mainly focused on the prevention of VVR of physiological origin, are still insufficient and can be optimized and complemented to reduce the occurrence of VVR, especially in first-time donors for whom anxiety and stress play an important role in the etiology of VVR. Two measures could further reduce the occurrence of VVR: Reinforcement of the physiological strategy: ingestion of a salty snack before donation, the effect of which could be similar to the effect of the isotonic solution, which could not be delivered in practice because of its cost following the data of the EVASION study. Addition of a psychological strategy: flyer given at the interview presenting the four most frequent fears as well as a description of the recommended muscular and respiratory exercises, followed by the execution of the recommended exercises before the sampling. Hypothesis is that the combination of a psychological and physiological strategies would allow a reduction of the occurrence of immediate and/or 48 h delayed VVR during the whole blood donation in first time donors compared to the current practices.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vasovagal Reaction
Keywords
first time donor, whole blood donation, vasovagal Reaction, physiological, psychological, BDRI, BDAS

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5320 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
No Intervention
Arm Description
EFS usual standard practices for the whole blood donation
Arm Title
Test Group 1
Arm Type
Experimental
Arm Description
A psychological strategy is added to EFS standard practices before the whole blood donation flyer given at the interview presenting the 4 most frequent fears as well as a description of the recommended muscular and breathing exercises, followed by a training of these exercises and their execution
Arm Title
Test Group 2
Arm Type
Experimental
Arm Description
A physiological strategy is added to EFS standard practices before the whole blood donation : - Ingesting a salty snack.
Arm Title
Test group 3
Arm Type
Experimental
Arm Description
The both psychological and physiological strategies are added to EFS standard practices before the whole blood donation flyer given at the interview presenting the 4 most frequent fears as well as a description of the recommended muscular and breathing exercises, followed by a training of these exercises and their execution Ingesting a salty snack.
Intervention Type
Other
Intervention Name(s)
Psychological strategy
Intervention Description
flyer given at the interview presenting the 4 most frequent fears as well as a description of the recommended muscular and breathing exercises, then realization accompanied by a training of these exercises
Intervention Type
Other
Intervention Name(s)
Physiological strategy
Intervention Description
- ingesting a salty snack
Primary Outcome Measure Information:
Title
Vasovagal reactions (VVR)
Description
Proportion of first-time donors experiencing VVR (immediate and delayed up to 48 hours) during whole blood donation managed by both psychological and physiological strategies (group 4) compared to usual standard practices (group 1)
Time Frame
Day 1 = donation day ; Day 3 = 48h post donation
Secondary Outcome Measure Information:
Title
VVR psychological strategy
Description
Proportion of first-time donors experiencing VVR (immediate and delayed up to 48 hours) during whole blood donation managed by psychological strategy (group 2) compared to usual standard practices (group 1)
Time Frame
Day 1 = donation day ; Day 3= 48h post donation
Title
VVR physiological strategy
Description
Proportion of first-time donors experiencing VVR (immediate and delayed up to 48 hours) during whole blood donation managed by physiological strategy (group 3) compared to usual standard practices (group 1)
Time Frame
Day 1 = donation day ; Day 3= 48h post donation
Title
Immediate VVR
Description
Proportion of first-time donors with immediate VVR compared between the groups
Time Frame
Day 1 = donation day, before leaving the centre
Title
Delayed VVR
Description
Proportion of first-time donors with delayed VVR compared between the groups
Time Frame
Day 3= 48h post donation
Title
First-time donor adherence
Description
Adherence of the primary donor to the study strategies and to the EFS recommendations (complete intake of salty snacks, hydration, performance of muscle and breathing exercises training, performance of muscle and breathing exercises during donation, compliance with the duration of post-donation monitoring stage).
Time Frame
Day 1 = donation day, before leaving the centre
Title
Anxiety/fear
Description
Assessment of the evolution of the "anxiety/fear" score between arrival and before the whole blood donation, compared between the groups. This questionnaire consists of the 6-item Blood Donor Anxiety Scale (BDAS) (5-point Likert scale) (Chell et al., 2016) and a 4-item component with a 5-point Likert scale that allows for an assessment of the 4 most common donor fears (of the needle, to see blood, to feel pain, to experience sensations of discomfort). The scoring is obtained by summing up the responses to the different items. Score is between 10 and 50, a higher score is associated to a better outcome.
Time Frame
Day 1 = donation day, before donation
Title
Sense of control and fears
Description
Assessment of the "sense of control and fears" score, compared between the groups. The concepts measured here are the feeling of control related to giving blood (5 items) and the feeling of control over fears (4 items) according to a 5-point Likert scale. The scoring is obtained by summing up the answers to the different items. Score is between 9 and 45, a higher score is associated to a better outcome.
Time Frame
Day 1 = donation day, before donation
Title
Feelings of discomfort
Description
Assessment of the "feelings of discomfort" score, compared between the groups. The BDRI (Blood Donation Reactions Inventory) (France et al., 2008) provides an assessment of the subjective evaluation of 11 pre-syncopal symptoms (5-point Likert scale). The BDRI is easily understood by donors and is rapid. The BDRI provides important information about the donor experience to predict satisfaction and likelihood of re-donation. The score is calculated by summing up the responses to the various items. Score is between 11 and 55, a higher score is associated to a worse outcome.
Time Frame
Day 1 = donation day, after donation and before leaving the centre
Title
First-time donor retention
Description
Compared between the groups the number of first-time donors who made a second blood donation in the 12 months following the first-time donation, collected by query from the EFS computerized file
Time Frame
Month 12 following the first-time donation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: M/F between 18 and 70 years old, A first-time donor who wishes to donate blood in Lyon, either at a fixed site or at a mobile unit, Declared fit to donate whole blood after the EFS pre-donation interview, Weight ≥ 50kg and height ≥ 135 cm, Available for telephone contact between to 5d +/- 2 days after donation, Having signed a written consent to participate in the study. Non-inclusion criteria: Known allergy to shellfish, and/or gluten, and/or milk, and/or soy, Incomprehension of the French language, First-time donor under protective measures (guardian, curator) or any other administrative measure, Not affiliated to the French social security system or any other equivalent system, Pregnant or breastfeeding woman, Subject participating in any other interventional or non-interventional research Exclusion Criteria: Withdrawal of consent First-time donor with anemia following routine hemoglobin testing First-time donor not reachable for telephone interview
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Brice MD POREAU
Phone
478 656 137
Ext
+33
Email
brice.poreau@efs.sante.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Julie MD-PhD HAESEBAERT
Phone
472 115 732
Ext
+33
Email
julie.haesebaert@chu-lyon.fr
Facility Information:
Facility Name
French Blood Establishment (EFS)
City
Lyon
ZIP/Postal Code
69153
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brice MD POREAU, MD/PhD
Phone
478 656 137
Ext
+33
Email
brice.poreau@efs.sante.fr

12. IPD Sharing Statement

Plan to Share IPD
No

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Prevention of Vasovagal Reactions in First-time Blood Donors Using a Combined PSYchological and Physiological Approach

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