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OpenTrials
Completed

NCT Number: NCT06670027

The Effects of Use of Auditory Stimulation Methods on Cardiac Patients' Clinical Outcomes

This study will be used to compare the effects of two auditory stimulation methods on improving vital signs parameters, reducing the severity of chest pain, and improving the sleep quality of cardiac patients.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of nursing Damanhour university

Damanhūr, Egypt

About this study

This study aims to To evaluate the relative efficacy of two auditory stimulation techniques in enhancing cardiac patients' vital sign assessments.

  • This study aims to examine two auditory stimulations for their ability to alleviate chest pain in patients with heart conditions.
  • The goal of this study is to evaluate two audio stimulations for their potential to help heart patients have a better night's rest.

This research made use of two different therapies including audio stimulation. Group A used familiar auditory stimulus, which was a spoken message, and group B used sounds of nature.

Patients with preexisting cardiac conditions who were admitted to a predetermined critical care unit and who subsequently intended to have percutaneous coronary artery intervention (PCI)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • adult (aged≥18 years).
  • diagnosed with cardiac disease.
  • patient with hemodynamic stability
  • consciousness and ability to communicate.

Exclusion criteria

  • patients unable to comply with study interventions
  • patients with cognitive impairment
  • patients with severe unstable cardiac condition
  • having a history of hearing loss or the use of a hearing aid.

Treatment and study plan

Family voice

Other

Group A receives the family voice

Nature sound

Other

Group B receives the nature sound.

Primary outcomes

  1. sleep quality

    Time frame: three days after intervention

    sleep quality used Richards-Campbell Sleep Questionnaire (RCSQ). it consisted of five items score from zero mean poor pattern and 100 mean good

  2. severity of chest pain

    Time frame: three days after intervention

    Visual analogue scale consisted of score from 0 to 10 zero mean no pain and 10 mean high pain

  3. level of anxiety and depression

    Time frame: three days after intervention

    The hospital Anxiety and Depression (HAD) questionnaire consisted of 14 questions 7 for anxiety and 7 for depression score score 0-7 mean normal; score 8-10 mean mild; score 11-15, mean moderate; and score 16-21, mean severely

Sponsors and collaborators

Lead sponsor

Damanhour University

Other

Registry information

Official study title

The Effects of Using Auditory Stimulation Methods on Cardiac Patients' Clinical Outcomes

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Nov 1, 2024
Registry last updated
Jan 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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