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Completed

NCT Number: NCT02274064

Motivating Type O- Blood Donors to Return

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ohio University

Athens, Ohio, 45701, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • donor with New York Blood Center or Hoxworth Blood Center
  • one previous donation
  • O- or O+ blood
  • eligible to donate again

Treatment and study plan

Motivational Interview and Implementation Intention

Behavioral

Telephone call that includes motivational interviewing techniques and develops an implementation intention plan.

Primary outcomes

  1. 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

Secondary outcomes

  1. Donation attitude

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  2. Donation subjective norm

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  3. Donation perceived behavioral control

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  4. Donation intention

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  5. Donation decisional balance

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  6. Donor identity

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  7. Donation moral norm

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  8. Donation anticipated regret

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  9. Donation anxiety

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

  10. Donor self-efficacy (action and coping)

    Time frame: 1 week pre- and 1 week post-intervention

    questionnaire

Sponsors and collaborators

Lead sponsor

Ohio University

Other

Collaborators

  • Hoxworth Blood Center
  • New York Blood Center

Registry information

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Oct 24, 2014
Registry last updated
Sep 27, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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