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Study identifier: NCT07093307 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Docudrama for Blood Donation in Ghana (DDID)

Condition: Blood Donation  ·  Sponsor: University of Minnesota

PhaseNA
Planned participants180
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

A cluster pilot RCT to evaluate the effectiveness of the docudrama compared to a control group (usual engagement with blood services) on repeat blood donation attempts among first-time blood donors. Secondary outcomes will be blood donor retention, attitudes, subjective norms, perceived behavioral control and intention as potential mediators of blood donation behavior among first-time blood donors. The cluster pilot RCT will have two arms: 1) docudrama and 2) control. Randomization will stratify by the type of site: mobile versus fixed. Each participant in the docudrama arm will receive the intervention one time immediately after blood donation. Participants in both the docudrama arm and control arm will receive standard blood donor communications and will be followed for six months. Actualized blood donation is possible every four months using NBSG guidelines; however, blood donation sessions may not occur at the blood donation sites until six months. Return blood donation attempts will be evaluated using the Southern Zonal Blood Center (SZBC) records (primary outcome) and participant self-report (secondary outcome) at six months. Secondary measures will be evaluated at baseline and six months from enrollment. The duration of the study will be 11 months, allowing for five months to achieve enrollment goals and six months of follow-up for the last individual enrolled.

This description comes directly from the study's public registry record.

Talk to the study team

Susan E Telke, MS  ·  +1 612-590-2697  ·  telke001@umn.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Southern Zonal Blood Centre, National Blood Service GhanaAccra, GhanaRecruiting

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Source record: clinicaltrials.gov/study/NCT07093307