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

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.

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

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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