Validation of electronic (web-based and smartphone) administration of measures of pelvic floor dysfunction
Validation of electronic (web-based and smartphone) administration of measures of pelvic floor dysfunction
Sponsor: Internal
Enrolling: Male and Female Patients
Study Length: 3 Months
IRB Number: AAAO8451
Contact: Linda Hardy: 212-932-4309 / lh2158@cumc.columbia.edu
Additional Study Information: You will be randomly assigned to complete questionnaires via either a paper format, web-based format, or smartphone format. About 2 weeks later but before treatment begins, you will be asked to complete a different form of the questionnaire either in the office or at home. You will be emailed and/or called by research staff to remind you to complete the second set of questionnaires. If you are asked to complete bowel or bladder diaries as part of your treatment plan, you will be randomly selected to either complete these on the smartphone or paper and then two weeks later, you will be asked to complete it in the other format. You will be emailed and/or called by research staff to remind you to complete the second diary format.About 216 people are expected to be enrolled in this study from multiple sites, including 150 from Columbia UniversityMedical Center.
This study is closed
Investigator
Doreen Eleanor Chung, MD
Do You Qualify?
Do you have pelvic floor dysfunction? Yes No
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Place Holder




For more information, please contact:
Linda Hardy
lh2158@cumc.columbia.edu
212-932-4309