- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02274064
Motivating Type O- Blood Donors to Return
September 26, 2016 updated by: Christopher R. France, Ph.D., Ohio University
This study develops a motivational interview and implementation intention intervention for blood donor retention and tests the efficacy of this new approach among first-time, Group O donors.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In this study the investigators will recruit first-time Group O- and O+ donors four weeks after their donation using the donor databases of New York Blood Center and Hoxworth Blood Center.
Eligible donors will be contacted via email and invited to participate in the study.
Interested donors will be randomly assigned to either the Intervention condition where they will receive a motivational interview and implementation intention intervention phone call or to the Control condition where they will receive a standard donor recruitment phone call.
Outcome measures will be assessed before and after the telephone contact using online questionnaires, and donation attempts will be tracked for one year.
The investigators will use survival analysis to examine the effects of this intervention on retention during this one-year follow-up.
Path analyses will also be used to examine potential mediators of the intervention effect.
The investigators hypothesis is that donors who receive the motivational interview and implementation intention intervention will have larger increases in positive donation attitudes and perceived behavioral control which will contribute to enhanced intention and donation attempts.
Study Type
Interventional
Enrollment (Actual)
598
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
-
-
Ohio
-
Athens, Ohio, United States, 45701
- Ohio University
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- donor with New York Blood Center or Hoxworth Blood Center
- one previous donation
- O- or O+ blood
- eligible to donate again
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
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
Donors randomly assigned to this group will receive a motivational interview and implementation intention intervention telephone call.
|
Telephone call that includes motivational interviewing techniques and develops an implementation intention plan.
|
No Intervention: Control
Donors randomly assigned to this group will receive a standard donor recruitment telephone call.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Repeat donation
Time Frame: 1 year from the date of next donor eligibility (i.e., 13 months post-intervention)
|
number and timing of repeat donation attempts in one year following eligibility of donor return
|
1 year from the date of next donor eligibility (i.e., 13 months post-intervention)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Donation attitude
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation subjective norm
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation perceived behavioral control
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation intention
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation decisional balance
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donor identity
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation moral norm
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation anticipated regret
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donation anxiety
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
Donor self-efficacy (action and coping)
Time Frame: 1 week pre- and 1 week post-intervention
|
questionnaire
|
1 week pre- and 1 week post-intervention
|
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
November 1, 2014
Primary Completion (Actual)
August 1, 2016
Study Completion (Actual)
August 1, 2016
Study Registration Dates
First Submitted
October 21, 2014
First Submitted That Met QC Criteria
October 22, 2014
First Posted (Estimate)
October 24, 2014
Study Record Updates
Last Update Posted (Estimate)
September 27, 2016
Last Update Submitted That Met QC Criteria
September 26, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- R56HL119180 (U.S. NIH Grant/Contract)
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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