Utilization of a novel interactive mobile health platform to evaluate functional outcomes and pain following septoplasty and functional endoscopic sinus surgery
Initiatives
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This study evaluates the utility of a digital patient engagement platform to track patient‐reported outcome measures (PROMs) following septoplasty and functional endoscopic sinus surgery (FESS).
Note: All published information has been collected from the article referenced in the Marker Paper box below. Therefore, there may be variations with more advanced versions of the study.
- Start Year
- 2017
- Funding
- Funding sources for the study: No industry funding was provided for this study. The use of the application, HealthLoop, was provided by Northwestern Medicine as a pilot program for innovation in healthcare delivery.
Design
- Study design
- Patients' cohort
Marker Paper
Khanwalkar AR, Shen J, Kern RC, et al. Utilization of a novel interactive mobile health platform to evaluate functional outcomes and pain following septoplasty and functional endoscopic sinus surgery. Int Forum Allergy Rhinol. 2019;9(4):345‐351. doi:10.1002/alr.22273
PUBMED 30586227
Recruitment
- Sources of Recruitment
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- Individuals
Number of participants
- Number of participants
- 288
- Number of participants with biosamples
Access
Availability of data and biosamples
| Data | |
| Biosamples | |
| Other |
Timeline
US patients
A prospective cohort was recruited at a tertiary care center from January 2017 to March 2018. A mobile phone application relayed PROMs, including pain (assessed on a 0 to 10 visual analogue scale [VAS] every other day for 2 weeks, as well as the patient‐reported outcome measure information system [PROMIS] pain interference short form 4a at baseline, 2 weeks, and 3 months) and timing of return to work.
Selection Criteria
- Newborns
- Twins
- Countries
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- United States of America
- Ethnic Origin
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- Health Status
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- Patient after septoplasty and functional endoscopic sinus surgery
Recruitment
- Sources of recruitment
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- Specific population
- Specific Population
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- Clinic patients
Number of participants
- Number of participants
- 288
- Number of participants with biosamples
Data Collection Event
A mobile phone application relayed PROMs, including pain (assessed on a 0 to 10 visual analogue scale [VAS] every other day for 2 weeks, as well as the patient‐reported outcome measure information system [PROMIS] pain interference short form 4a at baseline, 2 weeks, and 3 months) and timing of return to work.
- Start Date
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2017-01
- End Date
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2018-03
- Data sources
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Mobile data collection
- Mobile phone
- Smartphone apps
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Mobile data collection