NCT02274064

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
598

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2014

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 21, 2014

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 24, 2014

Completed
8 days until next milestone

Study Start

First participant enrolled

November 1, 2014

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2016

Completed
Last Updated

September 27, 2016

Status Verified

September 1, 2016

Enrollment Period

1.8 years

First QC Date

October 21, 2014

Last Update Submit

September 26, 2016

Conditions

Blood Donors

Keywords

RetentionBlood Donor Motivation

Outcome Measures

Primary Outcomes (1)

  • Repeat donation

    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 Outcomes (10)

  • Donation attitude

    1 week pre- and 1 week post-intervention

  • Donation subjective norm

    1 week pre- and 1 week post-intervention

  • Donation perceived behavioral control

    1 week pre- and 1 week post-intervention

  • Donation intention

    1 week pre- and 1 week post-intervention

  • Donation decisional balance

    1 week pre- and 1 week post-intervention

  • +5 more secondary outcomes

Study Arms (2)

Intervention

EXPERIMENTAL

Donors randomly assigned to this group will receive a motivational interview and implementation intention intervention telephone call.

Behavioral: Motivational Interview and Implementation Intention

Control

NO INTERVENTION

Donors randomly assigned to this group will receive a standard donor recruitment telephone call.

Interventions

Motivational Interview and Implementation IntentionBEHAVIORAL

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

Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ohio University

Athens, Ohio, 45701, United States

Location

MeSH Terms

Interventions

Motivational Interviewing

Intervention Hierarchy (Ancestors)

Directive CounselingCounselingMental Health ServicesBehavioral Disciplines and ActivitiesHealth ServicesHealth Care Facilities Workforce and Services

Study Officials

  • Christopher R France, PhD

    Ohio University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Distinguished Professor

Study Record Dates

First Submitted

October 21, 2014

First Posted

October 24, 2014

Study Start

November 1, 2014

Primary Completion

August 1, 2016

Study Completion

August 1, 2016

Last Updated

September 27, 2016

Record last verified: 2016-09

Locations

US(1)