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The effect of reminiscence on delirium in patients admitted to intensive care units and intensive care syndrome in their family caregivers

The effect of reminiscence on delirium in patients admitted to intensive care units and intensive care syndrome in their family caregivers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251101067839N1
Enrollment
50
Registered
2025-11-11
Start date
2025-11-10
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Delirium. Delirium superimposed on dementia

Interventions

Intervention group: Intervention group: In addition to receiving standard intensive care care, patients in the intervention group will receive a reminiscence intervention for 5 days, 20 minutes a day,

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients admitted to the intensive care unit with a level of consciousness =10 GCS. It has been shown that patients with GCS <7 are unable to respond to cognitive stimuli such as reminiscence due to their very low level of consciousness. Patients age 18 years and older Obtaining informed consent from the patient or their legal guardian The presence of chronic cognitive impairment (such as dementia), severe psychiatric illness, and a previous diagnosis of chronic delirium in the patient Absence of cognitive impairment and severe psychiatric illnesses in family caregivers according to their own self-reports and those around them

Exclusion criteria

Exclusion criteria: Patients admitted to the intensive care unit with a GCS level of consciousness <10 Age under 18 years The presence of chronic cognitive impairment (such as dementia), severe psychiatric illness, and a previous diagnosis of chronic delirium in the patient The presence of cognitive impairment and severe psychiatric illnesses in family caregivers according to their own self-reports and those around them.

Design outcomes

Primary

MeasureTime frame
Severity of delirium in patients (measured with NEECHAM) and family intensive care unit syndrome in caregivers (measured with Family Intensive Care Units syndrome Inventory). Timepoint: Day 6 of the study compared to day zero (before the start). Method of measurement: Delirium Assessment Scale and Family Intensive Care Syndrome Questionnaire.

Secondary

MeasureTime frame
Level of consciousness, use of sedatives, and length of stay in the ICU. Timepoint: Day Zero to Day Six. Method of measurement: Level of consciousness variable with Glasgow Coma Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVajihe Zabihi

Mashhad University of Medical Sciences

Zabihiv4032@mums.ac.ir+98 51 3623 8022

Outcome results

None listed

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