Nonorganic sleep disorders. Nonorganic sleep disorders
Conditions
Interventions
Intervention 1: Intervention in the first treatment group included using blinders from 10 pm to 7 am since the second night of attending CCU. Intervention 2: Intervention in the second treatment group
Treatment - Other
Intervention in the first treatment group included using blinders from 10 pm to 7 am since the second night of attending CCU.
Intervention in the second treatment group included using earplugs from 10 pm to 7 am since the second night of attending CCU.
Intervention in the third treatment group included using both blinders and earplugs from 10 pm to 7 am since the second night of attending CCU.
Sponsors
Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion study: recognizing time; place and people; having no operation; having no visual or auditory problems; not using psychic medicine; having no mental disorders; having no known sleeping disorders; no addiction to drugs; not having disorders affecting sleeping such as migraine; staying CCU for at least 3 days; least GCS equal to 12; not having the patient intubed. Exclusion indexes: having serious problems being in CCU; quitting the study on patients will; cardiac-pulmonary revival throughout the study; receiving drugs which affect night sleep such as duretics ; prescribing sedative drugs.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: Beginning and end of attending hospital. Method of measurement: According to Pitsburg questionnaire.;Delirium range. Timepoint: Daily, since the second day of attending till leaving hospital. Method of measurement: According to dizziness evaluation questionnaire NEE CHAM.;During attending hospital. Timepoint: Leaving hospital. Method of measurement: According to patient profile.;Blood pressure. Timepoint: Daily during attending hospital. Method of measurement: Using an automatic pressure check equipment while seating from left arm.;Temperature. Timepoint: Daily during attending hospital. Method of measurement: Using a mercury thermometer in mouth.;Heart beats. Timepoint: Daily during attending hospital. Method of measurement: Using monitoring tools.;Breath counts. Timepoint: Daily during attending hospital. Method of measurement: Chest movement counts by an expert in one minute.;SPO2. Timepoint: Daily during attending hospital. Method of measurement: Using pals eximeter.;Consciousness level. Timepoint: Daily during attending hospital. Method of measurement: Considering three visual, verbal and motor response parameters. | — |
Countries
Iran (Islamic Republic of)
Outcome results
None listed