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The effects of sensory modification on delirium incidence and cognitive status in open heart surgery intensive care unit's patients

The effects of sensory modification on delirium incidence and cognitive status in open heart surgery intensive care unit's patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014121517237N6
Enrollment
120
Registered
2015-10-29
Start date
2015-10-23
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

Delirium. Other delirium (Postoperative delirium)

Interventions

Intervention 1: Intervention group: In addition to routine care, multidimensional intervention for sensory modification will be done including the use of blindfold (made of black cloth), earplugs (Mar
Prevention
Intervention group: In addition to routine care, multidimensional intervention for sensory modification will be done including the use of blindfold (made of black cloth), earplugs (Mark Elvex Quattro
Control group: without any intervention.

Sponsors

Vice Chancellor for research of Golestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Age between 18 and 65 years old 2. The lack of known visual disturbances 3. The lack of known hearing impairment 4. Absence of known psychiatric disorders 5. The lack of known motor disorders in limbs 6. Lack of delirium at baseline 7. Without preoperative cognitive impairment Exclusion criteria: 1. Patients who will be discharged or died during the study 2. The need for CPR during study 3. Patients dissuade for continuing to work with researchers 4. The need for re-operation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Delirium. Timepoint: Before and two days after intervention. Method of measurement: Using the NeaCham scale.

Secondary

MeasureTime frame
Cognitive status. Timepoint: From two to five days after operation. Method of measurement: By using the MMSE instrument.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Bakhshi

Golestan University of Medical Sciences

mostafa.darzi@yahoo.com+98 17 3436 8856

Outcome results

None listed

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