Encouraging Blood Donation in Patients With a Blood Type in Short Supply

Sponsor
Geisinger Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT05135325
Collaborator
(none)
59,093
1
4
6.7
8860.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Patient portal message
  • Behavioral: Social responsibility
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
59093 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Masking Description:
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.
Primary Purpose:
Health Services Research
Official Title:
Encouraging Blood Donation in Patients With a Blood Type in Short Supply
Actual Study Start Date :
Nov 15, 2021
Actual Primary Completion Date :
Jun 6, 2022
Actual Study Completion Date :
Jun 6, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: 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.

Behavioral: Patient portal message
Portal message encourages patients to donate blood

Experimental: 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.

Behavioral: Patient portal message
Portal message encourages patients to donate blood

Behavioral: Social responsibility
Message specifies that there is a shortage of the patient's blood type

No Intervention: Shortage control

This group will not receive a message.

No Intervention: No-shortage control

This group will not receive a message.

Outcome Measures

Primary Outcome Measures

  1. Number of Participants Who Attended a Donation Appointment [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.

Secondary Outcome Measures

  1. Number of Participants Who Successfully Donated Blood [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.

  2. Number of Participants Who Scheduled a Blood Donation Appointment [Within 2 weeks of the final message send date]

    Scheduled an appointment within 2 weeks of their message send date.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Geisinger Danville Pennsylvania United States 17822

Sponsors and Collaborators

  • Geisinger Clinic

Investigators

  • Principal Investigator: Amir Goren, PhD, Geisinger Clinic

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Geisinger Clinic
ClinicalTrials.gov Identifier:
NCT05135325
Other Study ID Numbers:
  • 2021-0476
First Posted:
Nov 26, 2021
Last Update Posted:
Jul 26, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Geisinger Clinic

Study Results

No Results Posted as of Jul 26, 2022