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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06670027
Enrollment
80
Registered
2024-11-01
Start date
2024-07-01
Completion date
2024-12-01
Last updated
2025-01-22

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

Conditions

Anxiety, Chest Pain, Sleep

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)

Interventions

OTHERFamily voice

Group A receives the family voice

Group B receives the nature sound.

Sponsors

Damanhour University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Intervention model description

Group A will receive a family voice message and Group B will be received nature sound

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
sleep qualitythree days after interventionsleep quality used Richards-Campbell Sleep Questionnaire (RCSQ). it consisted of five items score from zero mean poor pattern and 100 mean good
severity of chest painthree days after interventionVisual analogue scale consisted of score from 0 to 10 zero mean no pain and 10 mean high pain
level of anxiety and depressionthree days after interventionThe 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

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026