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Impact of sensory excitation performed by family members and nurses on the level of consciousness and vital signs in patients who are admitted to Intensive care unit and the general health of their families

Impact of sensory excitation performed by family members and nurses on the level of consciousness and vital signs in patients who are admitted to Intensive care unit and the general health of their families

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201204149469N1
Enrollment
73
Registered
2012-06-30
Start date
2012-03-20
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

head trauma. Focal brain injury, Epidural hemorrhage, Traumatic subdural hemorrhage, Traumatic subarachnoid hemorrhage, Intracranial injury with prolonged coma, Other intracranial injuries, Intracranial injury, unspecified

Interventions

Intervention 1: Second test group patient: Dying sensory excitation program will be delivered by nurses. It will be applied two hours a day at 4-5 pm and 8-9 pm to the test groups for six days. Inter
Treatment - Other
Second test group patient: Dying sensory excitation program will be delivered by nurses. It will be applied two hours a day at 4-5 pm and 8-9 pm to the test groups for six days.
Control group patient: do not received Dying sensory excitation program, received Routine care.
First test group patient: Dying sensory excitation program will be delivered by family members. It will be applied two hours a day at 4-5 pm and 8-9 pm to the test groups for six days.

Sponsors

Vice chancellor for research, Lorestan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria (patients): head injury - GCS 5 to 10 - age16 to 65 years - obtained informed consent to participate in the study from family members,... Exclusion criteria: discharge from the ICU before sixth day,... Inclusion criteria (family members): first-degree relatives - older than 18 years,... Inclusion criteria ( nurses): Trained Nurses

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patient's consciousness level. Timepoint: 5 minutes before intervention and 30 minutes after intervention. Method of measurement: Glasgow coma score.;Patient's vital signs. Timepoint: 5 minutes before intervention and 30 minutes after intervention. Method of measurement: Respiratory-cardiac monitoring system.;Family members general health. Timepoint: immediately before and after the 1st, 6th and 12th hourly intervention session. Method of measurement: GHQ.—

Secondary

MeasureTime frame
Hospitalization period in ICU. Timepoint: Number of days hospitalized. Method of measurement: Checklist.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Adinevand

Lorestan university of medical sciences

mohadineh@gmail.com+66 16200140

Outcome results

None listed

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