Blood Donation and Subjective Well-being

January 10, 2026 updated by: OUYANG Jian, Guangzhou Blood Center

The Relationship Between Blood Donation and Subjective Well-being

This study investigates the psychological effects of blood donation among adult donors at the Guangzhou Blood Center. The primary objective is to examine whether a brief gratitude-based intervention delivered after donation enhances donors' subjective well-being (SWB) and basic psychological need (BPN) satisfaction. Participants who complete a whole-blood donation are randomly assigned to either an Intervention group, receiving a standardized gratitude reinforcement message accompanied by a vignette emphasizing the life-saving impact of donation, or a Control group that receives no additional message. All participants complete questionnaires at Time 1 (immediately after donation) and at Time 2 (4-22 days later), assessing SWB and related psychosocial variables.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

601

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

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Successfully completed a whole-blood donation at the Guangzhou Blood Center during the study period.
  • Able to read and understand the study materials and provide informed consent.
  • Provided the correct answer to a control question in the questionnaire
  • Provided their phone number.
  • Donated blood was successfully supplied to the hospitals.

Exclusion Criteria:

  • Whole blood donors with positive or suspicious serological results.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: No Message
Participants in this group complete the standard post-donation procedure and receive no additional message or vignette. They complete the same questionnaires at Time 1 (post-donation) and Time 2 (4-22 days later) as the Intervention group. This arm serves as the comparison condition for evaluating the effect of the gratitude-based intervention on subjective well-being and related psychosocial outcomes.
Experimental: Gratitude-based intervention
Participants in this group receive a standardized gratitude-based intervention immediately after completing whole-blood donation. The intervention consists of (1) a written gratitude reinforcement message acknowledging the donor's contribution and emphasizing the life-saving impact of their donation, and (2) a brief vignette illustrating how donated blood benefits patients in need. The purpose of this intervention is to enhance donors' subjective well-being and psychological need satisfaction by reinforcing their sense of autonomy, competence, and relatedness. Participants complete questionnaires at Time 1 (post-donation) and Time 2 (4-22 days later).
A reminder to inform donors that their blood has saved patient's life in a questionnaire.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Score of Subjective Well-Being at Time 2
Time Frame: 4-22 days after donation

Subjective well-being (SWB) is assessed at follow-up using a validated multi-item measure capturing life satisfaction and affective well-being.

Affect-Adjective Scale (validated Chinese version): 9 items, each scored 1-7. Satisfaction with Life Scale (validated Chinese version): 5 items scored 1-7. An aggregate SWB score was calculated by standardizing and summing life satisfaction scores with positive affect scores and subtracting the negative affect score from them.

Scores range from low to high levels of well-being. The primary objective is to evaluate whether exposure to the gratitude-based intervention leads to higher SWB relative to the control condition.

4-22 days after donation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Re-Donation Rate within One Year
Time Frame: Up to 12 months after the initial donation
Actual re-donation rate is obtained from the Guangzhou Blood Centre's donation records. The variable indicates whether the participant returned for another whole-blood or component donation within one year.
Up to 12 months after the initial donation
Score of Subjective Well-being at Time 1
Time Frame: Immediately after donation

Baseline Subjective well-being (SWB) is measured using a validated multi-item measure capturing life satisfaction and affective well-being.

Affect-Adjective Scale (validated Chinese version): 9 items, each scored 1-7. Satisfaction with Life Scale (validated Chinese version): 5 items scored 1-7. An aggregate SWB score was calculated by standardizing and summing life satisfaction scores with positive affect scores and subtracting the negative affect score from them.

Scores range from low to high levels of well-being.

Immediately after donation
Score of Basic Psychological Needs Satisfaction at Time 1
Time Frame: Immediately after donation
Baseline basic psychological needs (BPN) satisfaction is measured using a 9-item Basic Psychological Needs Scale (validated Chinese version). The scale contains subscales for autonomy, competence, and relatedness, using a 7-point scale ranging from 1 (not at all true) to 7 (very much true). Each of the three subscales was averaged to form an index of general BPN satisfaction. This measure captures donors' immediate psychological experience following donation. Higher scores indicate greater psychological need satisfaction.
Immediately after donation
Score of Basic Psychological Needs Satisfaction at Time 2
Time Frame: 4-22 days after donation
The same basic psychological needs satisfaction (BPN) scale is administered at follow-up to examine changes after the intervention. It is measured using a 9-item Basic Psychological Needs Scale (validated Chinese version). The scale contains subscales for autonomy, competence, and relatedness, using a 7-point scale ranging from 1 (not at all true) to 7 (very much true). Each of the three subscales was averaged to form an index of general BPN satisfaction. Higher scores indicate greater psychological need satisfaction.
4-22 days after donation
Score of Blood Donation Intention at Time 1
Time Frame: Immediately after donation
Intention to donate blood again in the future at Time 1 is measured using a single self-report intention item rated from 1 (very unlikely) to 7 (very likely), with higher scores indicating stronger intention to donate. The same item is administered at Time 1 and Time 2 to assess changes over time and to examine potential effects of the intervention on future donation motivation.
Immediately after donation
Score of Blood Donation Intention Score at Time 2
Time Frame: 4-22 days after donation
Intention to donate blood again in the future at Time 2 is measured using a single self-report intention item rated from 1 (very unlikely) to 7 (very likely), with higher scores indicating stronger intention to donate. The same item is administered at Time 1 and Time 2 to assess changes over time and to examine potential effects of the intervention on future donation motivation.
4-22 days after donation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

January 18, 2022

Primary Completion (Actual)

March 12, 2022

Study Completion (Actual)

March 16, 2022

Study Registration Dates

First Submitted

January 15, 2022

First Submitted That Met QC Criteria

January 15, 2022

First Posted (Actual)

January 28, 2022

Study Record Updates

Last Update Posted (Estimated)

January 13, 2026

Last Update Submitted That Met QC Criteria

January 10, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • Blood donation and well-being

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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