Encouraging Blood Donation in Patients With a Blood Type in Short Supply
1 other identifier
interventional
59,093
1 country
1
Brief Summary
As of November 2021, partly due to the COVID-19 pandemic, there has been a months-long national shortage of several types of blood in the U.S. (O-Pos, O-Neg, A-Neg, B-Neg, and AB-Neg), which has extended to a local blood shortage within the Geisinger community. The broad aim of this collaborative healthcare operations quality improvement project is to determine whether a message indicating that a patient's own blood type is in short supply increases the likelihood that they will donate, compared to a message that mentions a blood shortage without referencing the patient's blood type, or no message at all. Scientists in Geisinger's Behavioral Insights Team (BIT), part of Geisinger's Steele Institute for Health Innovation, will collaborate with Miller Keystone, where Geisinger refers patients who wish to donate blood and from whom Geisinger receives blood for clinical purposes. Patients with one of the needed blood types will be randomized to receive 1) a message about a blood shortage that does not specify the blood types in short supply or their own blood type (no-blood-type message), 2) the same message modified slightly to specify the recipient's blood type, and to mention that their blood type is in short supply (blood-type message), or 3) no message (shortage control group). A second no-contact control group of patients without any of the needed blood types will also be observed (no-shortage control group). Both the blood-type and no-blood-type messages are informed by behavioral science, emphasizing supply needs in local hospitals and providing community-relevant examples of why someone might need blood (e.g., farming or industrial accidents). The BIT will compare how many patients in each group choose to donate blood. They hypothesize that: 1) patients who receive either message will be more likely to donate than patients who receive no message; and 2) patients who receive the blood-type message will be more likely to donate than those who receive the no-blood-type message. With respect to the latter hypothesis, informing the recipient that they have one of the needed blood types may increase their perception that they are in a semi-unique position to help someone in need as compared to a more general message that may suffer from a diffusion of responsibility effect.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 15, 2021
CompletedStudy Start
First participant enrolled
November 15, 2021
CompletedFirst Posted
Study publicly available on registry
November 26, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 6, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
June 6, 2022
CompletedJuly 26, 2022
July 1, 2022
7 months
November 15, 2021
July 25, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of Participants Who Attended a Donation Appointment
Attended a donation appointment within 6 weeks of their message send date, regardless of whether they donated. This outcome includes patients who were unable to donate for any reason (e.g. low hemoglobin) or patients who showed up to the appointment but decided to leave before donating.
Within 6 weeks of the final message send date
Secondary Outcomes (2)
Number of Participants Who Successfully Donated Blood
Within 6 weeks of the final message send date
Number of Participants Who Scheduled a Blood Donation Appointment
Within 2 weeks of the final message send date
Study Arms (4)
No-blood-type message
EXPERIMENTALThis group will receive a message that does not mention the patient's blood type, or that the patient's blood type is in short supply.
Blood-type message
EXPERIMENTALThis group will receive a message that mentions the patient's blood type and that states their blood type is in short supply.
Shortage control
NO INTERVENTIONThis group will not receive a message.
No-shortage control
NO INTERVENTIONThis group will not receive a message.
Interventions
Portal message encourages patients to donate blood
Message specifies that there is a shortage of the patient's blood type
Eligibility Criteria
You may qualify if:
- Documented blood type in short supply (for message groups and shortage control group)
- Documented blood type not in short supply (for no-shortage control group)
- Age 18+
You may not qualify if:
- Hemoglobin test result \< 12.5 within the 3 months prior to list creation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Geisinger Cliniclead
Study Sites (1)
Geisinger
Danville, Pennsylvania, 17822, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Amir Goren, PhD
Geisinger Clinic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Masking Details
- The patients in the study will not know that other messages are being sent to other patients, although they will see the text of their own message. Providers will be blind to patient conditions.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 15, 2021
First Posted
November 26, 2021
Study Start
November 15, 2021
Primary Completion
June 6, 2022
Study Completion
June 6, 2022
Last Updated
July 26, 2022
Record last verified: 2022-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- ANALYTIC CODE
- Time Frame
- The data will become available after publication of study results in a scientific journal and will be available as long as the Open Science Framework hosts the data.
- Access Criteria
- The data on the Open Science Framework will be open to anyone requesting that information.
Data with no personally identifiable information will be made available to other researchers on the Open Science Framework for transparency.