In: Nursing
The answer is "NO"
No physiological measurements were collected from the subjects for the purpose of this study
To collect data on the dependent
variable, a phone call was made to participants 30 days after their
index hospitalization to determine if they had an unplanned
readmission to the hospital within that 30 day period. For
participants that reported readmission, the PI reviewed their
hospital medical records for the admitting diagnosis
and reason for readmission.
At the designated time selected by
participants or within one week of hospital discharge, telephone
contact with all potential participants who expressed an interest
in the study and provided their contact information was made. At
that time, either the survey was administered, a voice mail message
left or an appointment made for another time, as some individuals
did not feel up to completing the 30 minute phone call at that
time. During the call, the PI or research assistant highlighted the
points of informed consent from the information sheet provided at
initial contact and included: (a) a statement that the study
involves research; (b) an explanation of the purpose of the
study;
(c) an explanation that there will be no direct benefits and no
anticipated risks to participation; (d) an assurance of
confidentiality, anonymity; and (e) an assurance of the
participant’s right to choose not to participate or to terminate
participation at any time.
Additionally, elements of the Health Insurance Portability and
Accountability Act Privacy Rule for release of protected health
information, in this study access to their medical records to
determine diagnosis if readmitted, was included as part of the
consent. When possible, telephone surveys were scheduled with the
research assistant that made initial in-person contact to improve
response rates.