Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Not Yet Recruiting NCT07867613

The Effect of White Noise on Sleep, Quality of Recovery, and Satisfaction in Patients Undergoing Laparoscopic Cholecystectomy

Conditions: Laparoscopic Cholecystectomy

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 64
Sponsor: Ataturk University

Summary

This randomized controlled trial aims to evaluate the effect of white noise on sleep, recovery quality, and satisfaction in patients undergoing laparoscopic cholecystectomy. In the postoperative period, patients encounter numerous physical and psychological stressors, such as pain, difficulty adapting to the hospital environment, immobilization, environmental noise, frequent nursing interventions, individual characteristics, and illness-related anxieties. These factors disrupt sleep patterns; a decline in sleep quality can negatively affect tissue healing, immune function, pain control, psychological well-being, and the overall recovery process. Consequently, patient satisfaction with the care process may also decrease. Although pharmacological methods are commonly used to manage postoperative insomnia, they are not always sufficiently effective and carry various limitations, such as sedation, drug interactions, and other adverse effects. Therefore, interest has grown in recent years regarding non-pharmacological interventions that are safe, cost-effective, easy to implement, and carry a low risk of side effects. White noise, one such intervention, can create a more favorable sleep environment by masking irregular environmental sounds, promote relaxation, and has the potential to improve sleep quality.

Eligibility Criteria

Inclusion Criteria: * Being 18 years of age or older,Undergoing laparoscopic cholecystectomy, * Being conscious, oriented, and cooperative, * Having no hearing impairment, * Having no condition that would prevent listening to white noise, * Having no physical condition that would prevent the use of a smartwatch, * Being in a stable general condition, * Volunteering to participate in the study. * Having no diagnosed psychiatric, neurological, or cognitive disorder. * Having no diagnosed sleep disorder and not regularly using sleep medication Exclusion Criteria: * Conversion from laparoscopic surgery to open surgery, * Developing a serious postoperative complication,

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07867613). StuddyBuddy aggregates publicly available trial information.