RECRUITING

Comparing Use of Incentive Spirometry with and Without Reminder

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Conditions

Post OperativeIncentive spirometrycompliance

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Comparing Post Operative Utilization of Incentive Spirometry with and Without Electronic Patient Reminder

Quick Facts

Study Start:2024-01-16
Study Completion:2025-07-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06101030

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patient has undergone a qualifying surgical procedure.
  2. * Patient is aged 18 years or over.
  3. * 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.
  4. * Patient is able to comply with all study required incentive spirometry instructions.
  5. * 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.
  1. * Patients meeting any of the following exclusion criteria at baseline will be excluded from study participation:
  2. * Vulnerable Populations (Pregnant, minors, prisoners, those with significantly reduced mental acuity).
  3. * Patients where incentive spirometry is inappropriate (patients with Tractotomy, patients who are hemodynamically unstable, patients in reverse isolation due to infection).
  4. * 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.
  5. * Any medical condition that, in the opinion of the investigator, would place the patient at increased risk if they participated.
  6. * Any Physician determination that the patient should not participate.

Contacts and Locations

Study Contact

Michael Martin, RN
CONTACT
18582121728
michael@tidalmed.tech
Mehdi Arani
CONTACT
mehdi@tidalmed.tech

Principal Investigator

Hassan Study Director, M.D.
STUDY_DIRECTOR
Tidal Medical Technologies

Study Locations (Sites)

Tidal Reseach Site
Silver Spring, Maryland, 20904
United States
Tidal Study Site
Rochester, Minnesota, 55905
United States
Tidal Study Site
New Brunswick, New Jersey, 08901
United States

Collaborators and Investigators

Sponsor: Tidal Medical Technologies

  • Hassan Study Director, M.D., STUDY_DIRECTOR, Tidal Medical Technologies

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-16
Study Completion Date2025-07-07

Study Record Updates

Study Start Date2024-01-16
Study Completion Date2025-07-07

Terms related to this study

Keywords Provided by Researchers

  • Incentive spirometry
  • Post Operative
  • compliance

Additional Relevant MeSH Terms

  • Post Operative