Determining the effect of inhibiting visual and auditory stimuli during night sleep

Determining the effect of inhibiting visual and auditory stimuli during night sleep on the amount of analgesic medication required

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230506058100N3

Enrollment

Registered

2024-07-14

Start date

2024-07-22

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

burn. Burns of multiple regions, unspecified degree

Interventions

Intervention 1: Intervention group: During the 48 hours of examining the patients, during night sleep from 22:00 to 6:00, light and sound stimuli will be controlled with the help of ear muffs and blin

Eligibility

Sex/Gender

All

Age

15 Years to 55 Years

Inclusion criteria

Inclusion criteria: Age between 15-55 years Burn percentage between 30 and 60 consciousness Having a sleep disorder The minimum stay of the patient in the Intensive Care Unit is expected to be eight days and nights

Exclusion criteria

Exclusion criteria: Vision or hearing impairment History of addiction Mental disorder Sleep apnea Head and face burns Phobia of the dark

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 6 am, after a night's sleep, for 48 hours. Method of measurement: Numeric scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEbrahim Eskandari

Iran University of Medical Sciences

dreskandari2016@gmail.com+98 21 6435 2222

Outcome results

None listed

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