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The effect of implementing sensory stimulations program on clinical outcomes of brain injury patients admitted in Intensive Care Unit

The effect of implementing sensory stimulations program on clinical outcomes of brain injury patients admitted in Intensive Care Unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120414009469N4
Enrollment
66
Registered
2021-05-08
Start date
2021-06-21
Completion date
Unknown
Last updated
2021-05-26

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

Conditions

Condition 1: Head trauma. Condition 2: Head trauma. Condition 3: Head trauma. Condition 4: Head trauma. Condition 5: Head trauma. Condition 6: Brain Injury. Focal traumatic brain injury Diffuse traumatic brain injury Epidural hemorrhage Traumatic subdural hemorrhage Traumatic subarachnoid hemorrhage Intracranial injury

Interventions

Intervention 1: Intervention group: Sensory simulations program (Include: olfactory stimulation, auditory stimulation, Vision Stimulation, Tactile stimulation, Motor stimulation, awakening stimulation

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 67 Years

Inclusion criteria

Inclusion criteria: The patient with brain injury Intubated and under ventilator GCS score between 6 and 12 having pupillary reflex Age between 18 and 67 years.

Exclusion criteria

Exclusion criteria: Having a history of mental illness and hospitalization in a mental hospital; More than 2 days have passed since the patient is admitted to the ICU; Having a history of debilitating underlying diseases such as kidney, heart and liver failure; History of alcohol and opioid addiction; Having delirium

Design outcomes

Primary

MeasureTime frame
Type and Incidence rate of delirium. Timepoint: During the patient's hospitalization in the ICU, Daily. Method of measurement: Confusion Assessment Method for the Intensive Care Unit (CAM-ICU).;Severity of pain. Timepoint: 5 minutes before intervention and 5 minutes after intervention. Method of measurement: Behavioral Pain Scale.;Consciousness level. Timepoint: 5 minutes before intervention and 5 minutes after intervention. Method of measurement: Glasgow coma score.

Secondary

MeasureTime frame
Dependence on mechanical ventilation period. Timepoint: Number of days dependence on mechanical ventilation. Method of measurement: Checklist.;Incidence rate of death. Timepoint: During hospitalization time. Method of measurement: Checklist.;Hospitalization period in Intensive Care Unit. Timepoint: Number of days hospitalized in Intensive Care Unit. Method of measurement: Checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Adineh

Ahvaz University of Medical Sciences

mohadineh@gmail.com+98 61 3554 2036

Outcome results

None listed

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