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Clinical Trials/NCT06670027
NCT06670027
Completed
Not Applicable

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

Damanhour University1 site in 1 country80 target enrollmentJuly 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Damanhour University
Enrollment
80
Locations
1
Primary Endpoint
severity of chest pain
Status
Completed
Last Updated
last year

Overview

Brief Summary

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.

Detailed Description

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)

Registry
clinicaltrials.gov
Start Date
July 1, 2024
End Date
December 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

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

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

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

Study Sites (1)

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