Evaluating Interventions to Improve Stem Cell Donor Availability

Last registered on January 28, 2026

Pre-Trial

Trial Information

General Information

Title
Evaluating Interventions to Improve Stem Cell Donor Availability
RCT ID
AEARCTR-0017571
Initial registration date
January 21, 2026

Initial registration date is when the trial was registered.

It corresponds to when the registration was submitted to the Registry to be reviewed for publication.

First published
January 28, 2026, 6:53 AM EST

First published corresponds to when the trial was first made public on the Registry after being reviewed.

Locations

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Primary Investigator

Affiliation
University of Cologne

Other Primary Investigator(s)

Additional Trial Information

Status
In development
Start date
2026-01-21
End date
2029-12-31
Secondary IDs
Prior work
This trial does not extend or rely on any prior RCTs.
Abstract
This study tests whether behavioral narrative video interventions increase stem cell donors’ availability for confirmatory typing (CT). The research includes five arms: three narrative video treatments (targeting reciprocity, community, and “zero cost”), one non-narrative information video, and one plain no-video control. The primary outcomes are (i) stated CT availability (self-reported) and (ii) actual CT availability.
External Link(s)

Registration Citation

Citation
Ndiaye, Yero Samuel. 2026. "Evaluating Interventions to Improve Stem Cell Donor Availability." AEA RCT Registry. January 28. https://doi.org/10.1257/rct.17571-1.0
Experimental Details

Interventions

Intervention(s)
Behavioral narrative interventions and one video treatment designed to increase stem cell donor availability for confirmatory typing.
Intervention Start Date
2026-01-22
Intervention End Date
2027-12-31

Primary Outcomes

Primary Outcomes (end points)
Stated CT availability, Actual CT availability
Primary Outcomes (explanation)

Secondary Outcomes

Secondary Outcomes (end points)
Survey completion rates (1), knowledge about extraction methods (2), contact information updates (3), absence reporting (4), actual CT availability (5)
Secondary Outcomes (explanation)

Experimental Design

Experimental Design
This RCT tests whether behavioral narrative interventions increase stem cell donors’ availability for confirmatory typing (CT). The study uses five arms: three narrative video treatments, one video control, and one plain (no-video) control, and evaluates effects on both stated and actual CT availability. The narratives target reciprocity, community, and “zero cost.” The primary outcomes are (i) stated CT availability (self-reported) and (ii) actual CT availability.
Experimental Design Details
Not available
Randomization Method
Computer-generated random assignment
Randomization Unit
Individual donor-level
Was the treatment clustered?
No

Experiment Characteristics

Sample size: planned number of clusters
NA
Sample size: planned number of observations
Planned sample sizes follow the invitation split of 1.8M total invitations: Plain control (no video): 40,000 invitations Each of the four video arms (3 narrative treatments + 1 video control): 440,000 invitations each (total 1,760,000) Assuming 8% survey completion, the planned number of observations for stated CT availability (survey completers) is: Plain control: 40,000 × 0.08 = 3,200 Each video arm (T1, T2, T3, video control): 440,000 × 0.08 = 35,200 Total stated-outcome N: 144,000 Assuming 2% CT requests among completers over two years, the planned number of observations for actual CT availability (among CT requests) is: Plain control: 3,200 × 0.02 = 64 Each video arm (T1, T2, T3, video control): 35,200 × 0.02 = 704 Total CT-request N: 2,880
Sample size (or number of clusters) by treatment arms
The experiment has five arms: three narrative video treatments (T1–T3), one video control, and one plain (no-video) control. We will send 1,800,000 invitations in total. The plain control receives 40,000 invitations; the remaining 1,760,000 invitations are allocated equally across the four video arms (440,000 each).
Assuming an 8% survey completion rate, the expected number of observations for survey-based outcomes (stated CT availability) is 3,200 in the plain control and 35,200 in each video arm, for a total of 144,000 completed surveys.
Assuming a 2% CT request rate among survey completers over two years, the expected number of observations for behavioral outcomes (actual CT availability among CT requests) is 64 in the plain control and 704 in each video arm, for a total of 2,880 CT requests.
Minimum detectable effect size for main outcomes (accounting for sample design and clustering)
(1) Stated CT availability (1.1) Planned comparisons: 3 treatments vs. video control Using a Bonferroni-adjusted α = 0.0167 for the family of three comparisons and 80% power, with 35,200 participants per group, the minimum detectable standardised mean difference is Cohen’s d = 0.0244. (1.2) Video control vs. plain (without video) control Assuming a two-sided t-test with α = 0.05 and 80% power, and n = 35,200 (video control) vs. n = 3,200 (plain no-video control), the minimum detectable effect is Cohen’s d = 0.0517. (2) Actual CT availability (binary; among CT requests) (2.1) Planned comparisons: 3 treatments vs. video control Using a Bonferroni-adjusted α = 0.0167 for the family of three comparisons and 80% power, with 704 observations per group and a baseline rate of 80%, the minimum detectable difference in proportions is 0.0642 (6.42 pp.).
IRB

Institutional Review Boards (IRBs)

IRB Name
RESEARCH ETHICS REVIEW FACULTY OF MANAGEMENT, ECONOMICS, AND SOCIAL SCIENCES UNIVERSITY OF COLOGNE
IRB Approval Date
2025-10-08
IRB Approval Number
240124YN