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Evaluation of anxiety using faces anxiety scale in ICU patients using noise ablating headphones during night time versus ICU patients receiving usual care

Evaluation of anxiety using faces anxiety scale in ICU patients using noise ablating headphones during night time versus ICU patients receiving usual care.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032030
Enrollment
100
Registered
2021-03-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Control Intervention1: To evaluate whether reduction of stressful ICU noise during night time has some effect on patientâ??s anxiety levels over the course of their stay in ICU: This study seeks to ex

Sponsors

Rouble Jalota
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Eligible patients are any patients in ICU who could interact even intermittently in order to respond to questions about their feelings and emotions , opened their eyes in response to hearing their name or spontaneously or are awake , understand Hindi and have sufficient corrected vision to see Faces scale. These patients must be admitted in ICU for atleast 48 hours.

Exclusion criteria

Exclusion criteria: Patients having: a)severe to profound hearing loss. b)head or oromaxillofacial trauma. c)Baseline use of hearing aids. d)any other contradiction to use of ear plugs or headphones.

Design outcomes

Primary

MeasureTime frame
Study seeks to examine the effects of overnight noise reduction in ICU patients. Subjects will randomly be placed in two groups. receiving usual care ( control group) Standard nose ablating headphones applied from 11pm to 6am nightly for atleast four nights or until ICU discharge. In morning patients will be asked to grade their anxiety as shown in Faces Anxiety Scale. Assessment will be done for four days of their stay in ICU or until they are transfered to their respective wards. Timepoint: Study seeks to examine the effects of overnight noise reduction in ICU patients. Subjects will randomly be placed in two groups. receiving usual care ( control group) Standard nose ablating headphones applied from 11pm to 6am nightly for atleast four nights or until ICU discharge. In morning patients will be asked to grade their anxiety as shown in Faces Anxiety Scale. Assessment will be done for four days of their stay in ICU or until they are transfered to their respective wards.

Secondary

MeasureTime frame
Secondary: Effect on the requirement of sedatives in ICU during the course of their stay. Timepoint: Secondary: Effect on the requirement of sedatives in ICU during the course of their stay.This will be viewed for atleast for days of their ICU stay that whether the requirement of sedatives increase or decrease on putting noise ablating headphones during night time.

Countries

India

Contacts

Public ContactDr M Parvez Khan

King George Medical University

mpk_786@yahoo.com9839070724

Outcome results

None listed

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