Blood Donation and Subjective Well-being

Sponsor
Guangzhou Blood Center (Other)
Overall Status
Completed
CT.gov ID
NCT05213130
Collaborator
(none)
626
1
2
1.9
334.3

Study Details

Study Description

Brief Summary

Studies have suggested a positive relationship between prosociality and well-being. attempt to analyze the relationship between blood donation and subjective well-being, and try to figure out the moderators and mediators. Also, the investigators would like to compare difference of subjective well-being between donors who are explicitly presented with information that the participants' blood has saved patient's life and those who are not.

Condition or Disease Intervention/Treatment Phase
  • Other: Information
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
626 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
The Relationship Between Blood Donation and Subjective Well-being
Actual Study Start Date :
Jan 18, 2022
Actual Primary Completion Date :
Mar 12, 2022
Actual Study Completion Date :
Mar 16, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Information group

In this group, blood donors will receive a questionnaire 15-25 days after their blood donation, i.e., after their blood has been sent to the hospital and be transfused by patients. The questionnaire contains items measuring empathy, altruism, subjective well-being, etc., as well as a clear reminder to inform donors that their blood has saved patient's life.

Other: Information
A reminder to inform donors that their blood has saved patient's life in a questionnaire.

No Intervention: Non-information group

In this group, blood donors will receive a questionnaire 15-25 days after their blood donation, i.e., after their blood has been sent to the hospital and be transfused by patients. The questionnaire contains items measuring empathy, altruism, subjective well-being, etc., but there will be no reminder to inform donors that their blood has saved patient's life.

Outcome Measures

Primary Outcome Measures

  1. The scores of the subjective well-being in the questionnaire [1 day]

    Donors' self-rated average scores of the subjective well-being items, the higher score the better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Whole blood donors with negative serological results.
Exclusion Criteria:
  • Whole blood donors with positive or suspicious serological results.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Guangzhou Blood Center Guangzhou Guangdong China 510095

Sponsors and Collaborators

  • Guangzhou Blood Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
OUYANG Jian, Senior Investigator, Guangzhou Blood Center
ClinicalTrials.gov Identifier:
NCT05213130
Other Study ID Numbers:
  • Blood donation and well-being
First Posted:
Jan 28, 2022
Last Update Posted:
Mar 31, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 31, 2022