- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04484896
Message Framing on Recruiting Rh-D Negative Blood Donors
Effects of Message Framing on Recruiting Rh-D Negative Blood Donors in an Emergency Situation
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jian OU-YANG
- Phone Number: +8615918771924
- Email: 434524249@qq.com
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510095
- Recruiting
- Guangzhou Blood Center
-
Contact:
- Jian OUYANG, Master
- Phone Number: 0086 15918771924
- Email: 434524249@qq.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- O and A Rh- negative blood donors Last donations were between January 1, 2018 and December 31, 2019
Exclusion Criteria:
- With an obviously invalid phone number Serological results of the last donation were positive
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control group
Donors in this group were not received SMS reminders.
|
|
Experimental: Gain-frame Message
Short messaging service (SMS) message: Dear group O/A Rh-D negative blood donor: Hello! The inventory of group O/A Rh-D negative blood product is low at present, but patients with such blood group are in urgent need of blood. If you can, please consider donating blood again to save lives. Thank you for your support. Please bring your identification (ID) card and show this message to our staff. Thank you. |
Emergency recruitment cell phone short messages that emphasizing donating blood can save patients' lives were sent to donors in this group.
|
Experimental: Loss-frame Message
SMS message: Dear group O/A Rh-D negative blood donor: Hello! The inventory of group O/A Rh-D negative blood product is low at present, but patients with such blood group are in urgent need of blood. If you can, please consider donating blood again to prevent the loss of life. Thank you for your support. Please bring your ID card and show this message to our staff. Thank you. |
Emergency recruitment cell phone short messages emphasizing that donating blood can prevent patients from death were sent to donors in this group.
|
Experimental: Information Message
SMS message: Dear group O/A Rh-D negative blood donor: Hello! The inventory of group O/A Rh-D negative blood product is low at present, if you can, please consider donating blood again. Thank you for your support. Please bring your ID card and show this message to our staff. Thank you. |
Emergency recruitment cell phone short messages that only mentioning the low Rh-negative blood stockpile were sent to donors in this group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Re-donation rate
Time Frame: 7 days
|
Intention-to-treat were applied.
Re-donation rate was defined as the number of donors in each group divided by donors who re-donated within 7 days.
|
7 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Recruiting Rh-D- blood donors
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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