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Environmental Enhancements for Healthcare Facility Imaging Experience
N/A
Waitlist Available
Led By Michael V Knopp, MD, PhD
Research Sponsored by University of Cincinnati
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up temperature of the environment and of each participant may be monitored from the time the participant begins the environmental experience until the participant completes study procedures, up to roughly 1 hour
Awards & highlights
Study Summary
This trial is exploring how different environmental conditions and settings affect people's perceptions, and whether new technologies can help capture these perceptions.
Who is the study for?
This trial is for staff, volunteers, and patients over 18 at the Ohio State University who can consent to participate. Patients must have an imaging study scheduled at Wright Center. It excludes prisoners, non-English speakers, and those unable to consent without a guardian.Check my eligibility
What is being tested?
The study tests how different environmental factors like sound, light, smell, vibration, and voice activation in healthcare facilities affect patient experience and imaging quality. It also evaluates new biofeedback technologies for future clinical trials.See study design
What are the potential side effects?
Since this trial focuses on environmental perceptions rather than medical treatments or drugs, traditional side effects are not applicable. Participants may experience discomfort or stress from varied sensory conditions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ participants may complete physiological measurements through study completion, on average 1 year.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~participants may complete physiological measurements through study completion, on average 1 year.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Environmental preference
Feasibility of the use of voice activation within the imaging environment
Mood, Physiological State - Body Temperature
+2 moreSecondary outcome measures
Motion
Quality of imaging study
Temperature
Trial Design
3Treatment groups
Experimental Treatment
Group I: Staff populationExperimental Treatment5 Interventions
Staff participants who work in imaging-related healthcare environments will complete survey tools regarding their perception and preference of environmental factors and/or will participate in environmental experiences and provide feedback.
Group II: Patient populationExperimental Treatment5 Interventions
Patient participants will complete a survey tool and either participate in specific environmental experience testing or may be exposed to an environmental experience during the imaging examination. The imaging exam will be assessed in regard to quality factors such as motion artifacts as an indicator of being relaxed during the examination.
Group III: Healthy volunteer populationExperimental Treatment5 Interventions
Healthy volunteer participants will have one of two options for participation:
completion of an electronic survey tool to assess the perception and preference of environmental factors (virtual participation)
completion of the above survey and participation in environmental experiences and providing feedback about their experience (physical participation)
Find a Location
Who is running the clinical trial?
University of CincinnatiLead Sponsor
428 Previous Clinical Trials
634,371 Total Patients Enrolled
Ohio State UniversityLead Sponsor
829 Previous Clinical Trials
505,728 Total Patients Enrolled
Ohio Third FrontierOTHER
5 Previous Clinical Trials
676 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am an adult working at Ohio State University and can consent.I am 18 or older and can consent, or have a guardian who can, and I have an imaging study scheduled at the Wright Center.I am unable to give informed consent and do not have a legal guardian to do so for me.I cannot communicate in English.I am over 18 and can give my own consent or have a guardian who can.
Research Study Groups:
This trial has the following groups:- Group 1: Healthy volunteer population
- Group 2: Patient population
- Group 3: Staff population
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are any participants still enrolling in this trial?
"Per the clinicaltrials.gov page, this medical trial is actively recruiting participants. It was initiated on December 5th 2017 and last updated on April 15th 2022."
Answered by AI
What is the scope of involvement in this clinical trial?
"Affirmative. According to information found on clinicaltrials.gov, this medical study is actively seeking participants and was initially listed on December 5th 2017 with the latest update occurring in April 15th 2022. The experiment necessitates 1500 patients from a single site."
Answered by AI
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