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Comparison of the Effects of Organized Sensorry Stimulation Program by The Nurse and Family on level of Conciousness and Cognitive -Behavioral State in Head Injured Comatose Patients

Comparison of the Effects of Organized Sensorry Stimulation Program by The Nurse and Family on level of Conciousness and Cognitive -Behavioral State in Head Injury Comatose Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201111262621N9
Enrollment
60
Registered
2012-11-01
Start date
2010-05-01
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

Comatose Brain Injury. Multiple injuries of head

Interventions

Intervention 1: Sensory stimulation by the nurse in addition to the standard care. Sensory stimulation program covered 5 parts, namely awakening, auditory, visual, tactile and olfactory Sensory stimul
Rehabilitation
Sensory stimulation by the nurse in addition to the standard care. Sensory stimulation program covered 5 parts, namely awakening, auditory, visual, tactile and olfactory Sensory stimulation program co
Control group received standard care.
Sensory stimulation by a selected family member in addition to the standard care as above.

Sponsors

Research vice chancellor of Shiraz Univesity of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: i) State of coma at least from the previous three days; ii) age above 17 years; iii) Glasgow score (GCS) 3-8; iiii) Ranchlos score (RLA) I-II; iv) stable vital signs. Exclusion criteria: age above 60 years; opium and drug addiction; blindness; deafness and delusional disorder.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
GCS for Level of conciousness. Timepoint: The day before the study and seven days in the afternoon. Method of measurement: A double blind numerical scales are used with all patients observation.

Secondary

MeasureTime frame
RlA, WNSS for Cognitive-Behavioral state. Timepoint: The day before the study and seven days in the afternoon. Method of measurement: patient observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Moattari

Shiraz University of Medical Sciences

moattari@yahoo.com ; moattarm@sums.ac.ir+98 71 1647 4250

Outcome results

None listed

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