Improving Health of Patients With Colon Cancer Following Surgery: A Trial of SA-ICAN Via Videoconferencing
NCT ID: NCT02301338
Last Updated: 2017-03-13
Study Results
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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TERMINATED
2 participants
OBSERVATIONAL
2014-11-30
2016-03-16
Brief Summary
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The study will compare more frequent follow-up of patients by videoconferencing to routine follow-up of patients. The investigators will compare each type of follow-up to see the effect on the number of times patients need to visit emergency rooms or need admission to hospitals. The study will also look at the difference between each type of follow-up on patients' quality of life and social support thirty days after hospital discharge.
The study will also measure satisfaction and acceptability of this intervention among those who had follow-ups by videoconference.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Usual Care
The patient will get instructions on: - Follow-up appointment date/time with your surgeon - Proper diet - Medications - Communicating concerning symptoms with the surgeon
The patient will answer questions on:
* Social support
* Quality of life
Usual care
Phone Calls
In addition to what the usual care group gets, the patient will also receive weekly phone calls by a geriatrics RN following hospital discharge.
The patient will answer questions on:
* Social support
* Quality of life
Usual care
Phone Calls
Interventions
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Usual care
Phone Calls
Eligibility Criteria
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Inclusion Criteria
* Newly diagnosed cancer.
* Referred to the geriatrics service for pre-operative evaluation before surgical resection of his/her tumor.
Exclusion Criteria
* Deafness , measured by the Hearing Handicap Inventory for the Elderly Screening Version (HHIE-S) \[16\], score equal or above 30. (appendix 5)
* Cognitive impairment (score of 0-1 in Mini-Cog Test).
* Nursing home resident.
* Planned hospital length of stay of one day or less.
65 Years
ALL
No
Sponsors
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Memorial Sloan Kettering Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Armin Shahrokni, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Memorial Sloan Kettering Cancer Center
Locations
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Memorial Sloan Kettering Cancer Center
New York, New York, United States
Countries
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Related Links
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Memorial Sloan Kettering Cancer Center
Other Identifiers
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14-213
Identifier Type: -
Identifier Source: org_study_id
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