NCT05227352

Brief Summary

Recharge Rooms are immersive, biophilic private spaces designed to ameliorate trauma, anxiety, and stress. They feature multisensory input that is inspired by nature, as has previously been found to confer physiological benefits. These environments include silk imitation plants, projected scenes of soothing natural landscapes, low lighting that is tailored in color to match the landscapes that are being projected, high definition audio recordings of nature sounds paired with relaxing music, and infusion of essential oils and calming scents. The aim is to investigate the physiological and mental health outcomes that the short and long term exposure to these rooms have on healthcare workers. The data will be collected through online surveys. No identifiable information will be assessed or collected. The plan is to have 60 participants.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
85

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 26, 2022

Completed
12 days until next milestone

First Posted

Study publicly available on registry

February 7, 2022

Completed
8 months until next milestone

Study Start

First participant enrolled

September 27, 2022

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 8, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 8, 2025

Completed
Last Updated

March 7, 2025

Status Verified

September 1, 2024

Enrollment Period

2.3 years

First QC Date

January 26, 2022

Last Update Submit

March 4, 2025

Conditions

Keywords

biophilic designmental healthcognitionPTSDanxietystress

Outcome Measures

Primary Outcomes (1)

  • Well-Being Index

    This assesses a variety of dimensions such as burnout, fatigue, mental and physical quality of life (QOL), depression and anxiety, and is used as a screening tool to assess residents at "high risk," who may be in distress, and who benefit from added resources and subsequent help seeking. It uses yes/no response categories, and a total score is calculated by adding the number of 'yes' responses. Full scale range from 0 to 7, with higher score indicating poorer health outcome, and a threshold score of 5 is used to identify "high risk" residents.

    6 weeks

Secondary Outcomes (16)

  • Generalized Anxiety Disorder 7 (GAD7)

    6 weeks

  • The Patient Health Questionnaire (PHQ-9)

    6 weeks

  • The Insomnia Severity Index (ISI)

    6 weeks

  • The Fatigue Severity Scale (FSS)

    6 weeks

  • Brief Resilience Scale (BRS)

    6 weeks

  • +11 more secondary outcomes

Study Arms (1)

Biophilic experience

EXPERIMENTAL

Healthcare workers will experience the biophilic-designed room

Behavioral: Biophilic design experience

Interventions

Recharge Rooms are immersive, biophilic private spaces featuring multisensory input that is inspired by nature.

Biophilic experience

Eligibility Criteria

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

You may qualify if:

  • Adults over the age of 18
  • Current healthcare employee of Mount Sinai Hospital or the Icahn School of Medicine at Mount Sinai

You may not qualify if:

  • Age under 18
  • Not employed by Mount Sinai or Icahn School of Medicine at Mount Sinai

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Recharge Room at Mount Sinai Hospital

New York, New York, 10029, United States

Location

MeSH Terms

Conditions

Psychological Well-BeingAnxiety DisordersStress Disorders, Post-Traumatic

Condition Hierarchy (Ancestors)

Personal SatisfactionBehaviorMental DisordersStress Disorders, TraumaticTrauma and Stressor Related Disorders

Study Officials

  • Mar Cortes, MD

    Icahn School of Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor Rehabilitation and Human Performance

Study Record Dates

First Submitted

January 26, 2022

First Posted

February 7, 2022

Study Start

September 27, 2022

Primary Completion

January 8, 2025

Study Completion

January 8, 2025

Last Updated

March 7, 2025

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

There is no plan to share IPD at this time.

Locations