Patient and Physician Intervention to Increase Organ Donation (DECIDE)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01697137|
Recruitment Status : Completed
First Posted : October 2, 2012
Last Update Posted : February 23, 2015
|Condition or disease||Intervention/treatment||Phase|
|Tissue and Organ Donation Communication||Behavioral: Participant Video and Provider Cueing||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||916 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Double (Participant, Outcomes Assessor)|
|Primary Purpose:||Health Services Research|
|Official Title:||Patient and Physician Intervention to Increase Organ Donation in Primary Care Settings|
|Study Start Date :||September 2012|
|Actual Primary Completion Date :||May 2014|
|Actual Study Completion Date :||May 2014|
No Intervention: Usual Care
Following enrollment, participants will visit with their primary care provider per usual.
Experimental: Participant Video and Provider Cueing
Participants will watch a video prior to meeting with their provider. Participants will then cue their providers to discuss organ donation with them.
Behavioral: Participant 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).
- Proportion of participants who consent to donate organs [ Time Frame: 1 Day ]Consent either on the electronic donor registry or by completion of a organ donor card.
- Proportion of participants who reported holding donation discussions with their primary care provider [ Time Frame: 1 Day ]
- Proportion of participants who were satisfied with time spent with their provider on the study date [ Time Frame: 1 Day ]Proportion of participants who were somewhat or very satisfied with the amount of time spent with their provider during the date of the study.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01697137
|United States, Ohio|
|The MetroHealth System|
|Cleveland, Ohio, United States, 44109|
|Principal Investigator:||John D Thornton, MD, MPH||Case Western Reserve University|