Mayo Clinic Upper Digestive Disease Survey

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

The Mayo Clinic Conduit Report Card Questionnaires have been created in order to have a consistent evaluation tools for patients undergoing esophageal reconstruction or treatment or patients that are experiencing an upper digestive disease in order to standardize and validate outcome measures. Data will be used to establish the validation of the questionnaires/survey. Data will also lead to the establishment of "normal" or expected scores for patients undergoing each type of esophagectomy procedure and for upper digestive diseases. Data will contribute to creating treatment algorithms for symptom management for upper digestive diseases and for post-operative complications and symptoms as well as contribute to pre-operative education.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients undergoing or having already undergone an esophagectomy or esophageal reconstruction.

Disqualifiers

None

Trial population

Patients undergoing or having already undergone an esophagectomy or esophageal reconstruction.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Mayo Clinic Upper Digestive Disease Survey on Paper

    Other intervention

    Mayo Clinic patients will be asked to complete the Mayo Clinic Upper Digestive Disease Survey at their one month surgical follow up visit and then every three months for 1 year after surgery, then with each surveillance clinic visit or a minimum of once per year for their lifetime. The questionnaire can be completed at their clinic visit, over the telephone, or by mail. The patient's medical record will also be reviewed to gather any other contributing information.

  • Upper Digestive Disease (UDD Monitor) App

    Other intervention

    Mayo Clinic and non Mayo Clinic patients can participate by loading the app through the app store. Patient consent will be completed in the app. Patients will be asked to complete questionnaires at their 1.5 month surgical or diagnosis follow up and then every three months for 1 year after their surgery or diagnosis, then with each surveillance clinic visit or a minimum of once per year for their lifetime or as long as they want to participate. for iOS: https://apps.apple.com/us/app/upper-digestive-disease/id6448756724 for Android: https://play.google.com/store/apps/details?id=com.mayoclinic.uddmobile\&pli=1

Treatment groups

1,000 Participants
are divided into 2 treatment groups
Group A: Esophagectomy/Esophageal Reconstruction/Treatment2 interventions
Group B: Upper Digestive Disease2 interventions

Trial outcomes

Primary outcomes

1

Completion of the Mayo Clinic Upper Digestive Disease Survey by patients at varying time points following surgery

Completed Mayo Clinic Upper Digestive Disease Survey will be analyzed and used to establish validation.

Time frame
1 year

Secondary outcomes

1

Establishment of "normal" or expected scores from the Mayo Clinic Upper Digestive Disease Survey

Completed Mayo Clinic Upper Digestive Disease Survey will be used in the establishment of "normal" or expected scores for patients undergoing each type of esophagectomy procedure at different time points following surgery.

Time frame
3 years

Other outcomes

Sponsors and contacts

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