Warning You have reached the maximum number of saved studies Listing a study does not mean it has been evaluated by the U. Federal Government. Read our disclaimer for details. Last Update Posted : July 30, Study Description. We hypotheses that: Patients in the MDASI-IVR plus triage group will have less symptom burden less symptom severity, less symptom related interference, and better satisfaction of symptom control, better physical and emotional well-being over the month of the trial compared to the control group.
Patients in the MDASI-IVR plus triage group will have more frequent documentation of symptom management in line with treatment guidelines compared to the control group.
Detailed Description:. FDA Resources. Arms and Interventions. Calls twice weekly, where the system will ask you to rate types of symptoms on a scale from 0 to A report of severe symptoms will be sent to your doctor or nurse.
Outcome Measures. Primary Outcome Measures : To study the effectiveness of the interactive voice response system IVRS , which is designed to send a report to a patient's doctor about severe symptoms they are experiencing. Secondary Outcome Measures : To study if systematic symptom assessment by the use of IVRS is another way to report symptoms rather than the usual method, which is calling the doctor when there is a problem. Eligibility Criteria. Information from the National Library of Medicine Choosing to participate in a study is an important personal decision.
Inclusion Criteria: Patients scheduled for thoracic surgery for NSCLC, esophageal cancer and lung metastasis Patients 18 years of age or older Men and women of all ethnic groups who are English-speaking, and Patients residing in the United States.
The IVR system is not yet available in other languages. The United States residency requirement MDACC is an international referral center will allow us to follow patients for the duration of the study. Exclusion Criteria: Patients with a current diagnosis of psychosis or dementia Patients who have difficulty understanding the intent of the study Patients who cannot complete the assessment tools independently.
Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
As you make your decision, we also recommend you reference our guide to key features to look for in an IRT. The faster they can be built and deployed, the faster your trial can start getting results. To get that speed, you need a state-of-the-art IRT platform that combines the fast set-up times of configurable systems with the flexibility of custom programming.
You need Cenduit. Eclipse : " Eclipse IRT serves as a platform for our extensible web application suite. IRT seamlessly integrates with other technology solutions, like Electronic Data Capture EDC , to allow you to easily inform data management teams to updates in your clinical trial. It is a full fledged RTSM Randomization and Trial Supply Management solution that tracks your product throughout the entire clinical trial including dispensing!
Basically, all three refer to the technology clinical research sites use to control patient randomization and drug supply in clinical trials. IVRS Interactive Voice Response Systems : Used before internet connections were commonplace at all sites, this technology allows site administrators to interact with a database by pressing keypad buttons on a phone.
The administrator follows voice prompts in order to enter in information. They can integrate with other systems automatically, so you can easily connect with patient data or lab eligibility results, for example. Patient management: With these systems, you can both register new patients and randomize patients into a trial.
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