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NCT01458509 · ClinicalTrials.gov registry record

Feasibility and Psychometric Properties of Paper vs. Web vs. Automated Telephone Administration of Patient Reported Outcome Surveys

A clinical trial, sponsored by Memorial Sloan Kettering Cancer Center.

Completed
Registry status
325
Enrollment target

NCT01458509: Completed study, sponsored by Memorial Sloan Kettering Cancer Center.

NCT01458509 is a clinical trial that has completed, run by Memorial Sloan Kettering Cancer Center. The registered enrollment target is 325 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01458509 has completed, sponsored by Memorial Sloan Kettering Cancer Center.

COMPLETED
Registry status
325 participants
Enrollment target

Study Summary

It can be difficult to obtain the perspective of patients who have had bowel surgery. This study is being done because the investigators are trying to find out whether patient-reported outcomes, (results reported to investigators by the patient), on a regular basis, will help the investigators provide better patient care and symptom management. Therefore, the purpose of this study is to determine if it is possible and if it is useful to their medical care for patients who have had bowel surgery to complete surveys about their symptoms on a regular basis. In this study the surveys are completed from home, by web or by telephone, every month for 6 months. The results of this study will guide the design of large research studies on cancer-related bowel function. The purpose of this study is to develop a bowel function questionnaire for patients with colorectal cancer. The questionnaire will be used in future clinical trials to assess bowel function.

Interventions

  • BEHAVIORAL surveys
  • BEHAVIORAL Surveys

Trial Details

FieldValue
Enrollment Target 325 participants
Start Date 2011-10-11
Est. Completion 2021-09-08

Sponsor

Memorial Sloan Kettering Cancer Center

1,884 total trials

What the Registry Record Tells You About NCT01458509

The ClinicalTrials.gov registry entry for NCT01458509 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 325 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 1,884 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which surveys is the first listed.

NCT01458509 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01458509 about?

NCT01458509 is a clinical study titled "Feasibility and Psychometric Properties of Paper vs. Web vs. Automated Telephone Administration of Patient Reported Outcome Surveys". It can be difficult to obtain the perspective of patients who have had bowel surgery. This study is being done because the investigators are trying to find out whether patient-reported outcomes, (results reported to investigators by the patient), on a regular basis, will help the investigators provi...

What is the current status of trial NCT01458509?

This trial is currently completed. The enrollment target is 325 participants. The study started on 2011-10-11. Estimated completion is 2021-09-08.

What interventions are being tested in trial NCT01458509?

The interventions under investigation include: surveys (BEHAVIORAL), Surveys (BEHAVIORAL).

Who is sponsoring clinical trial NCT01458509?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 1,884 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.