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Survey of effectiveness of a multifactorial intervention in prevent of delirium in hospitalized patients in the Intensive Care Unit Cardiac Surgery

Survey of effectiveness of a multifactorial intervention in prevent of delirium in hospitalized patients in the Intensive Care Unit Cardiac Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015011220645N1
Enrollment
96
Registered
2015-07-22
Start date
2015-01-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Postoperative Delirium. Other delirium, Postoperative Delirium

Interventions

Intervention 1: By convenience sampling patient selected in control and intervention groups. In each group, 48 samples recruited. Research tools included: assessment scale of turbulence, quietness Ri
Prevention
By convenience sampling patient selected in control and intervention groups. In each group, 48 samples recruited. Research tools included: assessment scale of turbulence, quietness Richmond "RASS" To
There was no intervention in the control group and only RASS and Neecham scale was used to assess delirium in the control group.

Sponsors

Vice chancellor for research, Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patient's satisfaction and fellows to participate in the survey; age18 years and over; lack of understanding and underlying disease such as dementia; lack of alcoholism; ability to communicate and understand the Persian language; being healthy vision and hearing or eliminating defects by using of eyeglasses or hearing aids; not having a constant infusion of sedatives; the availability of the patient's family; restlessness and lack of level -5 and -4 based on RASS; lack of taking psychotropic medication. Exclusion criteria: dispensing with sick; transfer the patient to a medical center or other center; start sedative drugs constant infusion; cardiopulmonary resuscitation and endotracheal intubation and died of patient.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Delirium. Timepoint: every day until the fourth day after surgery in both groups performed. Method of measurement: Neecham & RASS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Babaee

Qazvin University of Medical Sciences

rbabee@qums.ac.ir; rezababaee54@yahoo.com+98 28 3323 7267

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026