- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05135325
Encouraging Blood Donation in Patients With a Blood Type in Short Supply
25. juli 2022 opdateret af: Geisinger Clinic
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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
59093
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Pennsylvania
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Danville, Pennsylvania, Forenede Stater, 17822
- Geisinger
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- 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+
Exclusion Criteria:
- Hemoglobin test result < 12.5 within the 3 months prior to list creation
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: No-blood-type message
This 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.
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Portal message encourages patients to donate blood
|
|
Eksperimentel: Blood-type message
This group will receive a message that mentions the patient's blood type and that states their blood type is in short supply.
|
Portal message encourages patients to donate blood
Meddelelsen angiver, at der er mangel på patientens blodtype
|
|
Ingen indgriben: Shortage control
This group will not receive a message.
|
|
|
Ingen indgriben: No-shortage control
This group will not receive a message.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of Participants Who Attended a Donation Appointment
Tidsramme: Within 6 weeks of the final message send date
|
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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of Participants Who Successfully Donated Blood
Tidsramme: Within 6 weeks of the final message send date
|
Attended a donation appointment within 6 weeks of their message send date and successfully donated, excluding patients who were turned away from or left their appointment without donating.
|
Within 6 weeks of the final message send date
|
|
Number of Participants Who Scheduled a Blood Donation Appointment
Tidsramme: Within 2 weeks of the final message send date
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Scheduled an appointment within 2 weeks of their message send date.
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Within 2 weeks of the final message send date
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
15. november 2021
Primær færdiggørelse (Faktiske)
6. juni 2022
Studieafslutning (Faktiske)
6. juni 2022
Datoer for studieregistrering
Først indsendt
15. november 2021
Først indsendt, der opfyldte QC-kriterier
15. november 2021
Først opslået (Faktiske)
26. november 2021
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
26. juli 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
25. juli 2022
Sidst verificeret
1. juli 2022
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 2021-0476
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
Data with no personally identifiable information will be made available to other researchers on the Open Science Framework for transparency.
IPD-delingstidsramme
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.
IPD-delingsadgangskriterier
The data on the Open Science Framework will be open to anyone requesting that information.
IPD-deling Understøttende informationstype
- ANALYTIC_CODE
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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