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NCT00870233 · OUTCOME

Feasibility of Electronic Capture of Patient-reported Symptoms From Home Following Major Gynecologic Cancer Surgery

Outcomes From Home in Patients Recovering From Major Gynecologic Cancer Surgery: Measuring Symptoms and Health-related Quality of Life · Source last updated 2018-10-15

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
once pre-operatively and then weekly starting 7 days after surgery until the 6-week post-operative period has ended.

Groups in this outcome

GYN Pts Undergoing Surgery

This study will assess patient use of WEBCORE, an online system designed for cancer patients to self-record toxicity-related symptoms based on NCI Common Terminology Criteria for Adverse Events and global quality of life (QoL) by European Organization for Research and Treatment of Cancer (EORTC QLQ-C30). online platform WEBCORE: Enrollees will be sent weekly email reminders to login to WEBCORE from home. Participants will be expected to complete the questionnaire once pre-operatively and then weekly starting 7 days after surgery until the 6-week post-operative period has ended.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
GYN Pts Undergoing Surgery120

Reported measurements

Source class 1

Requested to be removed from study

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
GYN Pts Undergoing Surgery18Not reportedNot reportedNot reportedNot reported

Did not undergo lapartomy

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
GYN Pts Undergoing Surgery3Not reportedNot reportedNot reportedNot reported

Incompatible internet browser

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
GYN Pts Undergoing Surgery2Not reportedNot reportedNot reportedNot reported

Died

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
GYN Pts Undergoing Surgery1Not reportedNot reportedNot reportedNot reported

Completed preoperative session in STAR

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
GYN Pts Undergoing Surgery69Not reportedNot reportedNot reportedNot reported

Didn't complete preop, completed other surveys

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
GYN Pts Undergoing Surgery27Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        18
      title
      Requested to be removed from study
    2. measurements
      1. group Id
        OG000
        value
        3
      title
      Did not undergo lapartomy
    3. measurements
      1. group Id
        OG000
        value
        2
      title
      Incompatible internet browser
    4. measurements
      1. group Id
        OG000
        value
        1
      title
      Died
    5. measurements
      1. group Id
        OG000
        value
        69
      title
      Completed preoperative session in STAR
    6. measurements
      1. group Id
        OG000
        value
        27
      title
      Didn't complete preop, completed other surveys
denoms
  1. counts
    1. group Id
      OG000
      value
      120
    units
    Participants
groups
  1. description
    This study will assess patient use of WEBCORE, an online system designed for cancer patients to self-record toxicity-related symptoms based on NCI Common Terminology Criteria for Adverse Events and global quality of life (QoL) by European Organization for Research and Treatment of Cancer (EORTC QLQ-C30). online platform WEBCORE: Enrollees will be sent weekly email reminders to login to WEBCORE from home. Participants will be expected to complete the questionnaire once pre-operatively and then weekly starting 7 days after surgery until the 6-week post-operative period has ended.
    id
    OG000
    title
    GYN Pts Undergoing Surgery
param Type
COUNT_OF_PARTICIPANTS
reporting Status
POSTED
time Frame
once pre-operatively and then weekly starting 7 days after surgery until the 6-week post-operative period has ended.
title
Feasibility of Electronic Capture of Patient-reported Symptoms From Home Following Major Gynecologic Cancer Surgery
type
PRIMARY
unit Of Measure
Participants

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice