- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04078893
The Effect of Recruiting Inactive Blood Donors Using Different Means
October 18, 2019 updated by: Guangzhou Blood Center
The Effect of Recruiting Inactive Blood Donors Using Different Means : on "Need" or Just Keeping Communication
14098 inactive donors were randomly divided into three groups according to age, sex, blood donation frequency,time of last donation and blood donation site, one group acted as the control group, one will be recruited by telephone recruitment on "need", and one will just be called for improvement suggestions of blood donor service.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
14098
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
- Recruiting
- Guangzhou Blood Center
-
Contact:
- Jinyan Chen, MPH
- Phone Number: 5374 +862083593939
- Email: chenjinyanx@gmail.com
-
-
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
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- inactive donors during 2016-2018
Exclusion Criteria:
- inactive donors during 2016-2018 but not eligible to donate
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: control group
|
|
Experimental: on need group
|
using telephone to recruit inactive donors on two different methods
|
Experimental: communication group
|
using telephone to recruit inactive donors on two different methods
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
donate blood or not
Time Frame: 12 months
|
rate of donation after recruitment
|
12 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 (Anticipated)
October 20, 2019
Primary Completion (Anticipated)
November 29, 2019
Study Completion (Anticipated)
January 29, 2020
Study Registration Dates
First Submitted
August 27, 2019
First Submitted That Met QC Criteria
September 3, 2019
First Posted (Actual)
September 6, 2019
Study Record Updates
Last Update Posted (Actual)
October 21, 2019
Last Update Submitted That Met QC Criteria
October 18, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- recruit inactive blood donors
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
To compare the effect of recruiting inactive blood donors between on "need" and just keeping communication
IPD Sharing Supporting Information Type
- Study Protocol
- Statistical Analysis Plan (SAP)
- Informed Consent Form (ICF)
- Clinical Study Report (CSR)
- Analytic Code
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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