Virtual Reality in ICU - PARTNER

NCT ID: NCT06876168

Last Updated: 2025-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

32 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-07-02

Study Completion Date

2026-09-30

Brief Summary

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This project is designed to have patients participate in a virtual environment with various tasks such as breathing exercises, games to help the brain, and techniques that promote relaxation while hospitalized in the Intensive Care Unit (ICU). The participation in research will last about 5 days and take about 15 to 45 minutes each day.

Detailed Description

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This is a research study about interacting and engaging in strategies to promote relaxation, improve mood, and stimulate thinking in patients in the Intensive Care Unit (ICU) in the hospital; called PARTNER. PARTNER is played by using a readily available Virtual Reality headset while patients are in the ICU. The researchers hope to learn if engaging with exercises for emotional health and cognitive function reduces delirium and loneliness in the hospital. If patients agree, the patients will be asked to play PARNTER, with a Virtual Reality (VR) device to connect them to a virtual environment with games and/or relaxing scenes while in the ICU. The Virtual environment may include things such as breathing exercise, mindfulness training, and relaxation techniques.

Conditions

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Acute Respiratory Failure Sepsis

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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VR-PARTNER

Participants in ICU

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Admitted to ICU at University of Kentucky for acute respiratory failure, sepsis or other

Exclusion Criteria

* Are less than 18 years of age
* Have a pre-existing neurologic disorder
* Have a pre-existing emotional or personality disorder
* Have a history or active mental health disorder or disease
* Experienced an acute neurologic event (e.g., stroke)
* Are currently pregnant
* Are a prisoner
* Receiving hospice care
* Have existing open wounds or pressure ulcers on head or neck
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Center for Complementary and Integrative Health (NCCIH)

NIH

Sponsor Role collaborator

Kirby Mayer

OTHER

Sponsor Role lead

Responsible Party

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Kirby Mayer

Associate Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Kirby P. Mayer, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University of Kentucky

Locations

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University of Kentucky

Lexington, Kentucky, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Louisa A Summers, Ph.D.

Role: CONTACT

859-200-6008

Facility Contacts

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Louisa A Summers, Ph.D.

Role: primary

8592006008

Other Identifiers

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R43AT013038

Identifier Type: NIH

Identifier Source: secondary_id

View Link

97957

Identifier Type: -

Identifier Source: org_study_id

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