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Patient and Physician Intervention to Increase Organ Donation

Patient and Physician Intervention to Increase Organ Donation in Primary Care Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01697137
Acronym
DECIDE
Enrollment
916
Registered
2012-10-02
Start date
2012-09-30
Completion date
2014-05-31
Last updated
2015-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Communication, Tissue and Organ Donation

Brief summary

The number of persons on the national solid organ waiting list continues to increase while the number of donated organs has failed to keep pace. In some portions of northeastern Ohio the donation rate is as low as 32%. There is a positive association between discussing organ donation with a primary care physician and signing a donor card. However, such discussions are rare. The investigators propose a blinded randomized controlled trial to evaluate the effectiveness of two interventions: 1) showing a donation video to patients in primary care settings waiting to see their physician and 2) cueing of primary care providers to have donation discussions with their patients. The study will be conducted throughout Cuyahoga County in at least 10 ambulatory clinics associated with a single county medical system. Nine hundred patients over 15.5 years of age will be enrolled. The investigators hypothesize that patients exposed to the interventions will be 1) more likely to consent to donate organs, 2) more likely to have donation discussions with their primary care providers, and 3) equally satisfied with the time spent with their doctor compared to patients who are not exposed to the interventions.

Interventions

BEHAVIORALParticipant Video and Provider Cueing

Participants will watch a 5-minute video and then select a question about donation to discuss with their primary care provider (provider cueing).

Sponsors

Case Western Reserve University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
15 Years to 78 Years
Healthy volunteers
Yes

Inclusion criteria

* At least 2 visits with their primary care provider in the last 3 years * Not previously consented to organ donation * At least 15.5 years of age * Less than 78 years of age

Exclusion criteria

* Visually impaired * Cognitively impaired * Non-English speaking

Design outcomes

Primary

MeasureTime frameDescription
Proportion of participants who consent to donate organs1 DayConsent either on the electronic donor registry or by completion of a organ donor card.

Secondary

MeasureTime frame
Proportion of participants who reported holding donation discussions with their primary care provider1 Day

Other

MeasureTime frameDescription
Proportion of participants who were satisfied with time spent with their provider on the study date1 DayProportion of participants who were somewhat or very satisfied with the amount of time spent with their provider during the date of the study.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026