Retaining Donors and Increasing Donation Frequency
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|ClinicalTrials.gov Identifier: NCT00005721|
Recruitment Status : Completed
First Posted : May 26, 2000
Last Update Posted : April 11, 2016
|Condition or disease|
The study continued research previously funded as part of a National Research and Demonstration Center (NRDC) in Transfusion Medicine.
There were six components to the study. The first identified significant factors influencing regular blood donations by individuals with different donation histories - first-time, second-time, committed (frequent), and lapsed donors. The second component developed and assessed the validity of behavioral models to increase donor retention and to predict whether first and second time donors would contribute again. The third developed donor-retention interventions, especially for the first and second time donors. The fourth component identified homogeneous subgroups among first, second and committed donors who might be receptive to different types of intervention strategies to increase the frequency of their donations. The fifth component evaluated the success of cost-effectiveness of the new interventions compared to existing blood center maintenance strategies. The sixth identified whether or not donors had a limit or ceiling on how often they donated per year.
The investigators drew on two related social psychological theories to combine cognitive and behavioral approaches to blood donor retention and to use the findings to construct a multiattribute model of donor decision-making. A behavioral decision model was used to predict donor behavior prospectively and to target and direct the design of interventions to increase donor retention and the frequency of donations.
Approximately 33 percent of the total project supported the subproject on retaining donors.
|Study Type :||Observational|
|Study Start Date :||September 1990|
|Actual Primary Completion Date :||December 1993|
|Study Completion Date :||December 1994|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00005721