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Evaluation of Patient Functionality and Utility of Web-Based Personal Health History and Risk Assess

NCT ID: NCT00822822

Last Updated: 2013-11-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

17 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-03-31

Study Completion Date

2009-11-30

Brief Summary

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The purpose of this research study is to find out what Moffitt and Lifetime patients think of the electronic medical records process.

Detailed Description

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Patient will complete a questionnaire about their knowledge of computers and how long they think it will take them to finish the patient health history using a computer.

Patient will complete the electronic record carefully and tell us if they had any difficulties, questions or comments about the format.

Patient will answer a questionnaire about how well they liked or did not like using the electronic system to give their health history.

Participation in this study will take approximately 30 minutes to 1 hour.

Conditions

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Cancer Cancer Screening Patients Patient Volunteers

Keywords

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Questionnaire Electronic Health History

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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A

Health History Process

First Questionnaire

Intervention Type BEHAVIORAL

Complete questionnaire before completing health history

Health History

Intervention Type BEHAVIORAL

Complete electronic health history

Second Questionnaire

Intervention Type BEHAVIORAL

Complete questionnaire after completing electronic health history

Interventions

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First Questionnaire

Complete questionnaire before completing health history

Intervention Type BEHAVIORAL

Health History

Complete electronic health history

Intervention Type BEHAVIORAL

Second Questionnaire

Complete questionnaire after completing electronic health history

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* The breakdown of patients recruited by stratified dimensional sampling. Overall, we will attempt to equally recruit patients from the unique strata for each domain evaluation in this study. Patients health status will be determined by the ECOG Performance status . We assume that all patients being seen at the Lifetime Cancer Screening and Prevention center will be of good to fair health, while patients seen at the Cancer hospital will range from good- to- fair to poor health status. Gender is also used as a sampling factor because there are modules within this web-based health history forms that are specific for each gender.

Exclusion Criteria

* Respondents who refuse to participate or who become too ill at any point in the assessment, will be excluded. Non-English speaking patients will be excluded. Names and other identifying information will not be collected and all data will be reported in aggregate form. Due to the nature of our stratified samples strategy, some patients will be excluded if they meet the criteria for a recruitment stata, but that stata is full.
Minimum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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H. Lee Moffitt Cancer Center and Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Erin Siegel, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

H. Lee Moffitt Cancer Center and Research Institute

Locations

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H. Lee Moffitt Cancer Center & Research Institute

Tampa, Florida, United States

Site Status

Countries

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United States

Other Identifiers

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104330

Identifier Type: OTHER

Identifier Source: secondary_id

MCC-14731

Identifier Type: -

Identifier Source: org_study_id