Ohio University
Athens, Ohio, 45701, United States
NCT Number: NCT02274064
This study develops a motivational interview and implementation intention intervention for blood donor retention and tests the efficacy of this new approach among first-time, Group O donors.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Athens, Ohio, 45701, United States
In this study the investigators will recruit first-time Group O- and O+ donors four weeks after their donation using the donor databases of New York Blood Center and Hoxworth Blood Center. Eligible donors will be contacted via email and invited to participate in the study. Interested donors will be randomly assigned to either the Intervention condition where they will receive a motivational interview and implementation intention intervention phone call or to the Control condition where they will receive a standard donor recruitment phone call. Outcome measures will be assessed before and after the telephone contact using online questionnaires, and donation attempts will be tracked for one year. The investigators will use survival analysis to examine the effects of this intervention on retention during this one-year follow-up. Path analyses will also be used to examine potential mediators of the intervention effect. The investigators hypothesis is that donors who receive the motivational interview and implementation intention intervention will have larger increases in positive donation attitudes and perceived behavioral control which will contribute to enhanced intention and donation attempts.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Telephone call that includes motivational interviewing techniques and develops an implementation intention plan.
Time frame: 1 year from the date of next donor eligibility (i.e., 13 months post-intervention)
number and timing of repeat donation attempts in one year following eligibility of donor return
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Time frame: 1 week pre- and 1 week post-intervention
questionnaire
Ohio University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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