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The effect of planned sensory stimulation on the level of consciousness ,vital signs and Oxygen saturation in patients in patients admitted to the ICU

The effect of planned sensory stimulation performed by family members and nurses on the level of consciousness ,vital signs and Oxygen saturation in patients admitted to Intensive care unit

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160308026961N5
Enrollment
115
Registered
2018-07-04
Start date
2018-05-10
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Patients with head trauma. Unspecified injury of head

Interventions

Intervention 1: The first intervention group will receive sensory stimulation by a family member every day for 2 hours, from 4 to 5 in the evening and 8 to 9 in the night with 3 hours distance and for

Sponsors

Vice chancellor for research of Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Visitors are only the main members of the family (father, mother, spouse, child, sister, brother) and their age is over 18 years of age. Patients is hospitalized with head trauma (Types of brain hematomas and other lesions, except diffuse axon damage) The patient has pupil reflexes at the entrance to the ICU section. The level of patients consciousness be between 6 and 12 The patient already has no history of mental illness, GCS fluctuations within a few days prior to the trauma (the Delirium term in this research) It has not been more than 3 days passed since the patient's admitted to the Intensive Care Unit

Exclusion criteria

Exclusion criteria: History of admission to a psychiatric hospital Visitors younger than 18 years of age

Design outcomes

Primary

MeasureTime frame
The level of consciousness. Timepoint: 10 minutes before the intervention and 30 minutes after the intervention. Method of measurement: Using the Glasgow Coma Scale (GCS).;Vital signs. Timepoint: 10 minutes before the intervention and 30 minutes after the intervention. Method of measurement: Using a cardio-respiratory monitoring device and an oxilary thermometer.;Arterial oxygen saturation. Timepoint: 10 minutes before the intervention and 30 minutes after the intervention. Method of measurement: Using a cardio-respiratory monitor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShila Amini

Emam Reza Hospital

k.vafaee1360@gmail.com+98 834276301

Outcome results

None listed

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