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Effect of white noise on the pain of entube Patients

Effect of White Noise on the pain of Patients with Impairment of Consciousness in Neurology intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201006048951N1
Enrollment
46
Registered
2021-01-15
Start date
2020-01-10
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

Neurological patients with decreased level of consciousness.

Interventions

Intervention 1: Intervention group: Ten minutes before the intervention, pain intensity is assessed by the researcher with the help of pain behavioral instruments and physiological symptoms (pulse rat

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 18 to 60 years Hospitalization in the intensive care unit due to decreased level of consciousness Decreased level of consciousness to 7-13(FOUR score) Presence of pain in the patient based on BPS instrument No hearing problem (history of using hearing aids, ear surgery, deafness, history of tinnitus, working in a noisy environment ...) Do not take auto toxic drugs for more than a week Lack of expressing pain verbally Not receiving painkillers in the last 24 hours Hospitalization for at least one week Lack of quadriplegia, extensive facial injuries, and impaired muscle function Intubation of the patient Listen to music

Exclusion criteria

Exclusion criteria: Patients with surgical cases admitted to the intensive care unit

Design outcomes

Primary

MeasureTime frame
Patient pain level connected to mechanical ventilation. Timepoint: Ten minutes before the intervention and thirty minutes after the intervention for three consecutive days in the afternoon. Method of measurement: Behavioral pain scale.

Secondary

MeasureTime frame
Systolic blood pressure. Timepoint: 10 minutes before the intervention, 30 minutes after the intervention, 30 minutes after the intervention , Three consecutive days. Method of measurement: Observe the patient's pain behavior ? check vital signs from the monitor.;Diastolic blood pressure. Timepoint: 10 minutes before the intervention, 30 minutes after the intervention, 30 minutes after the intervention , Three consecutive days. Method of measurement: Observe the patient's pain behavior ? check vital signs from the monitor.;Arterial blood pressure. Timepoint: 10 minutes before the intervention, 30 minutes after the intervention, 30 minutes after the intervention , Three consecutive days. Method of measurement: Observe the patient's pain behavior ? check vital signs from the monitor.;Heart rate. Timepoint: 10 minutes before the intervention, 30 minutes after the intervention, 30 minutes after the intervention , Three consecutive days. Method of measurement: Observe the patient's pain behavior ? check vital signs from the monitor.;Respiration rate. Timepoint: 10 minutes before the intervention, 30 minutes after the intervention, 30 minutes after the intervention , Three consecutive days. Method of measurement: Observe the patient's pain behavior ? check vital signs from the monitor.;Percentage of blood oxygen saturation. Timepoint: 10 minutes before the intervention, 30 minutes after the intervention, 30 minutes after the intervention , Three consecutive days. Method of measurement: Observe the patient's pain behavior ? check vital signs from the monitor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZeynab Solimani

Ardabil University of Medical Sciences

Ajri.mehdi@gmail.com+98 45 3372 6085

Outcome results

None listed

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