Post OperativeDigital healthDevice
What this study is
This study is designed to determine if patients using an incentive spirometer with visual and auditory signals will increase their use of the incentive spirometer and prevent lung complications.
What's being tested
- Signal On
Intervention · DEVICE
InSee monitor patient signals are on.
Study details
- Official title
- Comparing Post Operative Utilization of Incentive Spirometry With and Without Electronic Patient Reminder
- Sponsor
- Tidal Medical Technologies
- Conditions
- Post Operative
- Enrolling
- 500 people
- Starts
- 2024-01-16
- Est. completion
- 2025-09-07
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Patient has undergone a qualifying surgical procedure.
- Patient is aged 18 years or over.
- Patient has incentive spirometry ordered or incentive spirometry must be part of the study site's standard of care which is implemented by hospital staff.
- Patient is able to comply with all study required incentive spirometry instructions.
- Patient is without severe hearing or impaired visual acuity deficiency such that they cannot hear or see the audible and visual signal for the InSee monitor.
You can't join if
- Vulnerable Populations (Pregnant, minors, prisoners, those with significantly reduced mental acuity).; Patients where incentive spirometry is inappropriate (patients with Tractotomy, patients who are hemodynamically unstable, patients in reverse isolation due to infection).; Patients with a history of prior non-compliance or the presence or history of psychiatric condition (including drug or alcohol addiction), or cognitive issue which would in the opinion of the investigator, make it difficult for the patient to comply with the study procedures or follow the investigators instructions.; Any medical condition that, in the opinion of the investigator, would place the patient at increased risk if they participated.; Any Physician determination that the patient should not participate.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (3)
2 openTidal Study Site
Rochester, Minnesota, United States
- William LeTourneau · Contact
RecruitingTidal Study Site
New Brunswick, New Jersey, United States
- Brian Raffel, DO · Contact
RecruitingTidal Reseach Site
Silver Spring, Maryland, United States
Terminated
Study team
Sponsor
Tidal Medical Technologies
Study ID InSee 202301
Study director
Hassan Study Director, M.D.
Tidal Medical Technologies
Have questions? The contacts above can answer them before you apply.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.