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The effect of sensory stimulation on the level of consciousness and physiological parameters

Effect of sensory stimulation programs on level of consciousness and Physiological parameters in patients with head injury in intensive care units

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014031116942N1
Enrollment
60
Registered
2015-11-25
Start date
2014-05-22
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

trumatic brain injury. For primary coding of intracranial injuries with associated fractures, reference should be made to the morbidity or mortality coding rules and guidelines in Volume 2.

Interventions

Intervention 1: For control group did not perform any intervention and Patients affected by normal environmental stimulations. Intervention 2: Interventions in intervention group is a program consist
Rehabilitation
For control group did not perform any intervention and Patients affected by normal environmental stimulations.
Interventions in intervention group is a program consisted of sensory stimulation including :Tactile Gustatory, olfactory,auditory, visual and Kinetic Stimulation.Intervention done by the researcher

Sponsors

Vice chancellor for research,Kerman University of Medical Sciences ,Physiology Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: diagnosis of head trauma, GCS 8 and less than 8, aged 15-65 years, the absence of sensory disorders in patients (impaired sense of hearing, sight, smell, touch and taste) Exclusion criteria included : cerebral ischemia (confirmed by imaging studies), cardiac arrest, more than 4 minutes after admission

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Level of Consciousness. Timepoint: Before and after each intervention. Method of measurement: GCS and FOUR score.;Blood pressure. Timepoint: Before and after each intervention. Method of measurement: mm Hg and by cuff pressure of bed side monitoring device.;Heart rate. Timepoint: Before and after each intervention. Method of measurement: number / minute and by bed side monitoring device.;Respiratory rate. Timepoint: Before and after each intervention. Method of measurement: number / minute.;Arterial oxygen saturation. Timepoint: Before and after each intervention. Method of measurement: In percentage terms, and by pulse oxymeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHakimeh Hosseirezai

Kerman University of Medical Sciences

H_m5664@yahoo.com+98 343205177

Outcome results

None listed

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