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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01653938
Other study ID # 2009-P-002083
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 2011

Study information

Verified date November 2020
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a randomized controlled trial of a CPR video decision aid in patients with advanced congestive heart failure (CHF).


Description:

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.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date
Est. primary completion date September 2012
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: 1. A diagnosis of advanced heart failure: - New York Heart Association Class III or IV (III: marked limitation in activity due to symptoms, even during less-than-ordinary activity; IV: severe limitations, experiences symptoms while at rest). AND - Two or more hospitalizations for heart failure in the last year. AND - Either a systolic blood pressure = 120 mm Hg OR Na = 135 mEq/L. 2. Ability to provide informed consent. 3. Ability to communicate in English. 4. Age 65 or older.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
video decision aid


Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary preferences preferences for cpr and intubation 5 minutes after survey
Secondary knowledge knowledge of cpr and intubation 5 minutes after survey
Secondary decisional conflict decisional conflict 5 minutes after survey
Secondary advance care planning documentation advance care planning in medical record by the end of one year
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