Evaluation of Patient Functionality and Utility of Web-Based Personal Health History and Risk Assess
This study has been completed.
Sponsor:
H. Lee Moffitt Cancer Center and Research Institute
Information provided by:
H. Lee Moffitt Cancer Center and Research Institute
ClinicalTrials.gov Identifier:
NCT00822822
First received: January 13, 2009
Last updated: October 29, 2010
Last verified: October 2010
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Purpose
The purpose of this research study is to find out what Moffitt and Lifetime patients think of the electronic medical records process.
| Condition | Intervention |
|---|---|
|
Cancer Cancer Screening Patients Patient Volunteers |
Behavioral: First Questionnaire Behavioral: Health History Behavioral: Second Questionnaire |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Evaluation of Patient Functionality and Utility of Web-Based Personal Health History and Risk Assessment |
Resource links provided by NLM:
Further study details as provided by H. Lee Moffitt Cancer Center and Research Institute:
Primary Outcome Measures:
- Create a system for collecting patient health histories that may be beneficial to patients and people receiving services at Moffitt Cancer Center or Lifetime Cancer Screening Center [ Time Frame: 1 hour per participant ] [ Designated as safety issue: No ]
| Enrollment: | 17 |
| Study Start Date: | March 2006 |
| Study Completion Date: | November 2009 |
| Primary Completion Date: | November 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
A
Health History Process
|
Behavioral: First Questionnaire
Complete questionnaire before completing health history
Behavioral: Health History
Complete electronic health history
Behavioral: Second Questionnaire
Complete questionnaire after completing electronic health history
|
Detailed Description:
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.
Eligibility| Ages Eligible for Study: | 30 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
People receiving services at Moffitt Cancer Center or Lifetime Cancer Screening Center
Criteria
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.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00822822
Locations
| United States, Florida | |
| H. Lee Moffitt Cancer Center & Research Institute | |
| Tampa, Florida, United States, 33612 | |
Sponsors and Collaborators
H. Lee Moffitt Cancer Center and Research Institute
Investigators
| Principal Investigator: | Erin Siegel, Ph.D. | H. Lee Moffitt Cancer Center and Research Institute |
More Information
No publications provided
| Responsible Party: | Erin Siegel, Ph.D., H. Lee Moffitt Cancer Center & Research Institute |
| ClinicalTrials.gov Identifier: | NCT00822822 History of Changes |
| Other Study ID Numbers: | MCC-14731, 104330 |
| Study First Received: | January 13, 2009 |
| Last Updated: | October 29, 2010 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by H. Lee Moffitt Cancer Center and Research Institute:
|
Questionnaire Electronic Health History |
ClinicalTrials.gov processed this record on May 23, 2013