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effect of nature phonics and voice of patient acquaintances on pain and vital criteria in patients with decreased consciousness

Comparison the effect of natural voice and family voice on pain and physiological indices in unconscious patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190908044729N1
Enrollment
105
Registered
2019-09-21
Start date
2019-10-12
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

unconscious patients. Coma

Interventions

Intervention 1: Intervention group: family voice, in this intervention, physiological indices such as respiratory rate, heart rate, blood pressure and arterial blood oxygenation were measured using a

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Minimum enrollment age is 18 years Patient with low level of consciousness (Glasgow coma score of 5-9) Lack of hearing (hearing loss) in the person No bandage or ear surgery Lack of paralysis in four organs of the body No hearing aids Pain in the patient based on CPOT instrument (minimum score of 1)

Exclusion criteria

Exclusion criteria: -fracture in diseased organs use of neuromuscular blockers high-dose painkillers and sedatives previous history of intensive care unit admission Unstable hemodynamic status

Design outcomes

Primary

MeasureTime frame
Pain: A pain score, which is measured by the CRITICAL-CARE PAIN OBSERVION TOOL criterion, ranging from 0 to 8. Its value is measured before and after the intervention. Timepoint: Immediately before and after the intervention for two weeks in the morning and evening. Method of measurement: CRITICAL-CARE PAIN OBSERVION TOOL Pain Assessment Tool.;Physiological indices: Physiological indices in this study are systolic and diastolic blood pressure, mean arterial blood pressure, heart rate, respiratory rate and arterial blood oxygen level, measured by monitoring device before and after intervention in the experimental and control groups. Timepoint: Immediately before and after the intervention for two weeks in the morning and evening. Method of measurement: Cardiovascular Monitoring Machine.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKaveh Ebadi

Tehran University of Medical Sciences

k-ebadi@razi.tums.ac.ir+98 21 6692 7171

Outcome results

None listed

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