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NCT06142825 Clinical Trial

Developing, Implementing and Evaluating Effective Community-facility Interactions to Improve Blood Availability and Transfusion in Three Distinct County Settings in Kenya

Blood Transfusion Clinical Trial

— CoBAnK  

Official title:
Developing, Implementing and Evaluating Effective Community-facility Interactions to Improve Blood Availability and Transfusion in Three Distinct County Settings in Kenya (CoBAnK): A Type III Hybrid Effectiveness-implementation Trial.

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06142825
Other study ID # B09
Secondary ID 5UH3HL151595-04
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2024
Est. completion date July 1, 2026

Study information
Verified date April 2024
Source University of Minnesota
Contact Collin M Van Ryn
Phone 6514724502
Email mcca0676@d.umn.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The strategy of the CoBAnK study is to establish and enable the function of Community-Facility Transfusion Committees (CFTCs) incorporating diverse representation involving hospital, community, and county leadership, to improve blood availability and transfusion at the point-of-care.

Description:

The strategy of the CoBAnK study is to establish and enable the function of Community-Facility Transfusion Committees (CFTCs) incorporating diverse representation involving hospital, community, and county leadership, to improve blood availability and transfusion at the point-of-care. The CFTC strategy will be evaluated across nine transfusing facilities across three counties in Kenya (two intervention and one control site in each county). While the intervention will be tested in "beta" facilities (i.e., facilities without a co-located blood bank) in each county, blood availability will also be measured in "alpha" facilities (i.e., facilities with co-located blood banks) in the three counties, which supply blood to the beta facilities.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 9
Est. completion date July 1, 2026
Est. primary completion date July 1, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Eligibility criteria for study sites (beta hospitals): - Transfusing hospital at level 3 or higher - Has conducted at least 20 blood transfusions in the preceding year - Does not have a KTTA-approved blood bank (regional or satellite) in the facility premises - Receives blood from a blood bank at an Alpha Facility in the same county

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Community-Facility Transfusion Committee (CFTC)
Community-Facility Transfusion Committees (CFTCs) are intended to incorporate diverse representation involving hospital, community, and county leadership, to improve blood availability and transfusion at the point-of-care.

Locations
Country Name City State
n/a

Sponsors (5)
Lead Sponsor Collaborator
University of Minnesota Center for Public Health and Development, Kenya (CPHD), National Heart, Lung, and Blood Institute (NHLBI), Strathmore University, University of Pittsburgh

Outcome
Type Measure Description Time frame Safety issue
Primary Met blood need The proportion of transfusion requests resulting in dispatch of blood products from the laboratory The time required for the hospital laboratory to process a request for blood for transfusion, up to two weeks.
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