NCT07845734

Brief Summary

The aim of this study is to evaluate the effect of viewing nature imagery accompanied by music on blood pressure and pain in intensive care unit patients compared with standard care. The questions to be answered within the scope of the research are: Does viewing nature imagery accompanied by music affect blood pressure in intensive care unit patients compared with standard care? Does viewing nature imagery accompanied by music affect pain levels in intensive care unit patients compared with standard care? Participants will: The patients will be divided into two groups: an intervention group and a control group. The intervention group will Patients in the intervention group will be exposed to nature imagery accompanied by music once daily for 30 minutes over five consecutive days. Blood pressure and pain levels will be assessed before, during, and after each session. The control group will continue with routine intensive care unit follow-up treatments.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
5mo left

Started Sep 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress3%
Sep 2026Mar 2027

First Submitted

Initial submission to the registry

September 22, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 29, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

September 30, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2027

Expected
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2027

Last Updated

September 29, 2026

Status Verified

September 1, 2026

Enrollment Period

5 months

First QC Date

September 22, 2026

Last Update Submit

September 22, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Visual Analog Scale

    The study by Hayes and Patterson (1921) is considered a foundational source for the widespread adoption of the VAS in modern clinical pain measurement. Its clinical use in pain assessment was subsequently popularized, particularly by Huskisson (1974). It represents pain on a scale ranging from 0 (no pain) to 10 (severe pain). The patient indicates the intensity of the pain they are experiencing by marking a point on the line. The measurement can be scored on a 0-10 scale or a 0-100 mm scale.

    VAS measurements: Before the nature imagery and music viewing session (baseline value) At the 15th minute of the session At the end of the session (30th minute) 15 minutes after the nature imagery and music viewing session

  • Blood Pressure

    Systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial pressure (MAP) will be evaluated as primary physiological variables in the study. The values will be measured using a bedside monitor.

    Before the nature imagery and music viewing session (baseline value) • At the 15th minute of the session • At the end of the session (30th minute) • 15 minutes after the nature imagery and music viewing session

Study Arms (2)

Intervention Group: Viewing Nature Imagery Accompanied by Music

EXPERIMENTAL

Patients in the intervention group will complete a Demographic Information Form and the Visual Analog Scale (VAS). Blood pressure will be measured using a bedside patient monitor. Patients will view nature scenery (e.g., forests, seas, lakes, and waterfalls) displayed on a tablet while listening to relaxing, wordless instrumental music through headphones. Vivaldi's classical compositions with a tempo of 60-80 beats per minute will be used. The intervention will be administered by an intensive care nurse once daily for 30 minutes over five consecutive days. Blood pressure and pain levels will be assessed before the intervention, at the 15th minute, immediately after the intervention, and 15 minutes after completion on each of the five days.

Other: Viewing Nature Imagery Accompanied by Music

Control Group: Usual care

NO INTERVENTION

atients in the control group will complete the Demographic Information Form and VAS. Blood pressure and pain levels will be assessed at the same time points as in the intervention group over five consecutive days. No additional intervention will be provided, and routine intensive care treatment and nursing care will continue.

Interventions

As part of the non-invasive intervention to be administered to the intervention group, patients will be shown nature and landscape visuals accompanied by music once daily for 30 minutes over a total of five consecutive days. The intervention will consist of nature-themed visuals-such as forests, seas, lakes, and waterfalls-paired with relaxing, instrumental, and wordless music played at a tempo of 60-80 beats per minute (BPM). Classical music compositions by Vivaldi will be selected for the musical component.

Intervention Group: Viewing Nature Imagery Accompanied by Music

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being 18 years of age or older, Having a Glasgow Coma Scale (GCS) score of ≥14, Being hemodynamically stable, Having adequate hearing and visual functions, Being able to verbally express pain, Having a stay in the intensive care unit of at least 5 days, Having no speech or communication problems.

You may not qualify if:

  • Being under the age of 18, Having a diagnosis of delirium, Presence of hemodynamic instability, Receiving high-dose vasopressor therapy, Being under sedation, Having severe hearing or visual impairment, Declining to participate in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Esra Başer Akın, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

September 22, 2026

First Posted

September 29, 2026

Study Start

September 30, 2026

Primary Completion (Estimated)

February 28, 2027

Study Completion (Estimated)

March 1, 2027

Last Updated

September 29, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share