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The Influence of Natural Sounds on the Well-being of Patients After Orthopaedic Surgery

Evaluating the Impact of Nature Soundscapes on Post-Operative Stress and Anxiety in Orthopedic Surgery Patients

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07090915
Enrollment
120
Registered
2025-07-29
Start date
2025-08-31
Completion date
2026-06-30
Last updated
2025-07-29

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

Conditions

Postoperative Stress

Brief summary

For many people, a stay in hospital can be associated with stress and anxiety, especially after surgery. In order to potentially make the stay more pleasant for patients in future, the investigators are conducting a study to investigate the use of natural sounds to promote relaxation. Participation in this study usually lasts until 3 days after the operation in hospital. If the participants decide to take part, the participants will be randomly assigned to one of two groups: The intervention group or the control group. In the intervention group, the participants will listen to different natural sounds twice a day. In the control group, the participants will not receive any nature sounds. During the stay, the participants will be given two questionnaires to fill in about how you feel. Participants assigned to the intervention group will additionallyreceive a short telephone interview 14 days after the operation.

Interventions

Modern audio technology is used to create a 3D natural atmosphere.

Sponsors

Michael Tobias Hirschmann
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. duly completed declaration of consent 2. the age of the patient is at least 18 years 3. only patients undergoing orthopaedic surgery

Exclusion criteria

1. deafness 2. severe cognitive impairment 3. chronic pain patient 4. pain catheter insertion during the trial period 5. psychiatric disorders (e.g. anxiety disorders, depression, post-traumatic stress disorder, ...) 6. severe postoperative complications 7. no consent to participate

Design outcomes

Primary

MeasureTime frameDescription
Depressions-Angst-Stress-Skalen (DASS-21)From the first day after surgery until the third day after surgery.0 to 63 (0 is best 63 is bad)

Secondary

MeasureTime frameDescription
Relaxation State Questionnaire (RSQ), to measure the RelaxationFrom the first day after the surgery to the third day after the surgery.10 to 50 (10 is not relaxed, 50 is most relaxed)
NRS, to measure the PainlevelFrom the first day after the surgery to the third day after the surgery.0 to 10 (0 is no pain, 10 is most pain)
NRS, to measure the sleep qualityFrom the first day after the surgery to the third day after the surgery.0 to 10 (0 is no sleep, 10 ist best sleep)

Countries

Germany

Contacts

Primary ContactDaniel Basic
daniel.basic@ksbl.ch004161 400 60 89

Outcome results

None listed

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