A Trial of a CPR Video in Heart Failure Patients
Recruitment status was: Recruiting
|Study Design:||Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Health Services Research
|Official Title:||A Randomized Controlled Trial of a CPR Video in Heart Failure Patients|
- preferences [ Time Frame: 5 minutes after survey ]preferences for cpr and intubation
- knowledge [ Time Frame: 5 minutes after survey ]knowledge of cpr and intubation
- decisional conflict [ Time Frame: 5 minutes after survey ]decisional conflict
- advance care planning documentation [ Time Frame: by the end of one year ]advance care planning in medical record
|Study Start Date:||April 2011|
|Estimated Primary Completion Date:||September 2012 (Final data collection date for primary outcome measure)|
|No Intervention: control group|
Experimental: Video Arm
Use of video decision aid in the experimental arm.
|Behavioral: video decision aid|
Aim 1: To compare the care preferences for CPR and intubation among subjects randomized to video and subjects randomized to the current standard of care without the video.
Hypothesis 1: Subjects randomized to the video intervention will be significantly more likely to opt against CPR and intubation compared to those who do not see the video.
Aim 2: To compare code-status documentation in the electronic medical records between subjects randomized to the video and those who are receiving the current standard of care without the video.
Hypothesis 2: Subjects randomized to the video are more likely to have their code status correctly documented in the electronic medical records compared to those who do not see the video.
Aim 3: To compare knowledge and decisional conflict of subjects randomized to video and subjects randomized to the current standard of care without the video.
Hypothesis 3: When compared to subjects randomized to the current standard of care, subjects in the video intervention group will have higher knowledge and lower decisional conflict (lower decisional conflict scores) when asked to choose CPR and intubation preferences.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01653938
|United States, Massachusetts|
|Massachusetts General Hospital||Recruiting|
|Boston, Massachusetts, United States, 02114|
|Contact: Angelo Volandes 617-643-4266 firstname.lastname@example.org|
|Principal Investigator: Angelo Volandes|