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Effect of ASMR and White Noise on Sleep Quality in Patients Undergoing Elective Lower Extremity Surgery

NCT07651228 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2026-06-16

No results posted yet for this study

Summary

This randomized controlled trial aims to evaluate the effects of Autonomous Sensory Meridian Response (ASMR) and white noise on postoperative sleep quality in patients undergoing elective lower extremity surgery. Postoperative sleep disturbances are common after orthopedic surgery and may negatively affect pain perception, recovery, and overall patient outcomes. Participants will be randomly assigned to one of three groups: ASMR intervention, white noise intervention, or control group. Patients in the intervention groups will listen to standardized 30-minute audio recordings before sleep during the postoperative period, while the control group will receive routine care with headphones only. Sleep quality will be assessed using the Richards-Campbell Sleep Questionnaire (RCSQ). The study aims to determine which non-pharmacological intervention is more effective in improving postoperative sleep quality.

Conditions

  • Postoperative Sleep Disturbance
  • Orthopedic Surgery Patients
  • Sleep Quality

Interventions

BEHAVIORAL

ASMR Audio Intervention

Standardized ASMR audio recordings administered for 30 minutes before sleep during the postoperative period.

BEHAVIORAL

White Noise Audio Intervention

Standardized white noise audio recordings administered for 30 minutes before sleep during the postoperative period.

Sponsors & Collaborators

  • muzeyyen ataseven

    lead OTHER

Principal Investigators

  • Müzeyyen Ataseven, PhD,RN · Medipol University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-09-05
Primary Completion
2026-11-05
Completion
2027-01-05

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07651228 on ClinicalTrials.gov