- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03741413
The Effect of Message Framing on Blood Donation-Study 1
May 2, 2020 updated by: OUYANG Jian, Guangzhou Blood Center
Saving a Life or Preventing a Death: the Effect of Message Framing on Blood Donation Among Rh Negative Donors
Rh negative blood group is a rare blood group in China, as it only accounts for 0.3-0.4
percent of the Han population.
Therefore, low inventory is often found in blood collection and supply agencies in many regions in China.
On July 18, 2018 blood stockpile of O-negative and B-negative in Guangzhou Blood Center reached the warning line, and we took measures for emergency recruitment.
O-negative and B-negative blood donors whose last donation dates were between January 1, 2015 and December 31, 2017 were identified and randomly assigned to three groups.
Three different recruitment text messages were send to these groups respectively.
At the same time, A-negative and AB-negative blood donors were marked as control group.
We observed the re-donation rates among four groups within three months.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
2074
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510095
- Guangzhou Blood Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 56 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Rh- negative blood donors whose last donations were between January 1, 2015 and December 31, 2017.
Exclusion Criteria:
- Donors with an obviously invalid phone number. Donors whose serological results of the last donation were positive.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Gain-frame SMS
SMS messages "Dear Rh negative blood donors: Hello!
As the Rh negative O/B blood stockpile is low now, but patients who are this blood type are in urgent need.
If you are available, we hope that you can offer a helping hand to save their lives.
Thank you for your support."
were send to donors in this group.
|
Emergency recruitment cell phone short messages that emphasizing donating blood can save patients' lives were sent to donors in this group.
|
|
Experimental: Loss-frame SMS
SMS messages "Dear Rh negative blood donors: Hello!
As the Rh negative O/B blood stockpile is low now, but patients who are this blood type are in urgent need.
If you are available, we hope that you can offer a helping hand to prevent them from death.
Thank you for your support."
were send to donors in this group.
|
Emergency recruitment cell phone short messages emphasizing that donating blood can prevent patients from death were sent to donors in this group.
|
|
Experimental: Control SMS
SMS messages "Dear Rh negative blood donors: Hello!
As the Rh negative O/B blood stockpile is low now, but patients who are this blood type are in urgent need.
If you are available, we hope that you can donate blood again.
Thank you for your support."
were send to donors in this group.
|
Emergency recruitment cell phone short messages that only mentioning the low Rh-negative blood stockpile were sent to donors in this group.
|
|
No Intervention: Control group
Donors in this group were not received SMS reminders.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Re-donation rate
Time Frame: 3 months
|
Intention-to-treat were applied.
Re-donation rate was defined as the number of donors in each group devided by donors who re-donated within 3 months.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 18, 2018
Primary Completion (Actual)
October 18, 2018
Study Completion (Actual)
October 18, 2018
Study Registration Dates
First Submitted
November 11, 2018
First Submitted That Met QC Criteria
November 11, 2018
First Posted (Actual)
November 14, 2018
Study Record Updates
Last Update Posted (Actual)
May 5, 2020
Last Update Submitted That Met QC Criteria
May 2, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- Message framing effect
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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