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Electronic Reporting of Symptoms After Surgery

Electronic Patient-Reported Outcomes in Patients Recovering From Ambulatory Cancer Surgery: Measuring Early Postoperative Symptoms

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02700256
Enrollment
135
Registered
2016-03-07
Start date
2015-12-04
Completion date
2019-10-21
Last updated
2019-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients Scheduled to Undergo Surgery on the Gynecology Service

Keywords

surgery, 15-315

Brief summary

The purpose of this pilot study is to find out if patients are willing to self-report symptoms in the first 5 days following discharge, or when they leave the hospital after ambulatory surgery (ambulatory surgery is when the patient has surgery and then goes home within 24 hours).

Interventions

BEHAVIORALsurvey

All patients will submit a baseline survey following enrollment onto study. After successful completion of the AXR or 24-hour discharge pathway, the consented patient will be contacted by email or telephone for 5 days following discharge from surgery.

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The patients must be undergoing surgery for an indication tracked within the Gynecologic AXR program or have an expected postoperative discharge within 24 hours of surgery. These surgical procedures typically include: minimally invasive hysterectomy or radical hysterectomy, salpingo-oophorectomies \[mentioned above\], and minimally invasive staging procedures. * The patient must have a phone number or an email address. * The patient must be willing to self-report postoperative symptoms over an automated phone system or via an online platform. * The patient must speak and read fluent English.

Exclusion criteria

* Non-English speaking patients * Patients unwilling to provide contact information (email or phone number)

Design outcomes

Primary

MeasureTime frameDescription
number of patients who respond to the surveryup to 5 days after surgeryA patient will be deemed a responder if they complete at least 5 of the 8 symptom items on at least 3 days postoperatively. The symptom assessment method will be deemed successful if 32 of the 50 patients respond.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026