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Efficacy of Non-pharmacological Intervention Protocol in Reducing the Incidence of Postoperative Delirium in Elderly Patients Admitted to Surgical Intensive Care Units

Efficacy of Non-pharmacological Intervention Protocol in Reducing the Incidence of Postoperative Delirium in Elderly Patients Admitted to Surgical Intensive Care Units

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20181201001
Enrollment
300
Registered
2018-12-01
Start date
2018-06-04
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Postoperative Delirium Postoperative Delirium Non-pharmacological

Interventions

This study is a quasi&#45
experimental before&#45
and&#45
after design. The eligible patients will be enrolled following the inclusion criteria and excluded by exclusion criteria. Those patients will be allocated into standard of cares group (pre cohort) and
all of the process of care is based on the discretion of the responsible attending staffs. In the POST cohort&#44
pharmacological intervention protocols are implemented to all patients once they are admitted to the SICU and continued for 28 consecutive days or until they are discharged from the SICU or death. In
delirium is screened using the Thai&#45
version Confusion Assessment Method for the ICU (CAM&#45
ICU) by well&#45
trained research assistances twice a day between 08:00 to 10:00 and 18:00 to 20:00. The screening is carried out within 24 hours after SICU admission. In case of positive CAM&#45
ICU&#44
delirium is diagnosed and subsequently classified as hyperactive&#44
hypoactive&#44
or mixed types. In the PRE cohort&#44
delirious patients are managed based on the discretion of the attending staffs. In the POST cohort&#44
delirious patients are managed according to the pharmacological protocol initiated by trained attending staffs&#44
SICU fellows and residents.
Experimental Behavioral
Non&#45

Sponsors

Department of Anesthesiology Faculty of Medicine Siriraj Hospital, Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Age of 65 years old or more 2.Admitted to two SICUs at Siriraj hospital within seven days following surgery 3.Anticipated LOS in SICU of more than 24 hours.

Exclusion criteria

Exclusion criteria: 1.Patients undergoing surgery for more than seven days 2.Non-surgical patients 3.Patients who cannot communicate in Thai language 4.Patients with severe visual and auditory impairment that preclude communication

Design outcomes

Primary

MeasureTime frame
Postoperative delirium at 28 consecutive days or until they are discharged from the SICU or death non-pharmacological intervention protocol

Secondary

MeasureTime frame
Delirium free day at 28 consecutive days or until they are discharged from the SICU or death non-pharmacological intervention protocol

Countries

Thailand

Contacts

Public ContactAnnop Piriyapatsom

Mahidol university

annop.pir@mahidol.ac.th0922819241

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026