NCT02301338

Brief Summary

The purpose of this study is to assess the impact of more frequent follow-up (by videoconference) of these patients. Videoconference is a method of communication over a distance. In this method, the patient will hear the person's voice (like on the telephone) and will see that person over video. 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.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Nov 2014

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2014

Completed
20 days until next milestone

First Submitted

Initial submission to the registry

November 21, 2014

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 25, 2014

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 16, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 16, 2016

Completed
Last Updated

March 13, 2017

Status Verified

March 1, 2017

Enrollment Period

1.4 years

First QC Date

November 21, 2014

Last Update Submit

March 8, 2017

Conditions

Keywords

VideoconferencingFollowing Surgery14-213

Outcome Measures

Primary Outcomes (1)

  • acute healthcare utilization (AHCU) rates

    (i.e. hospital readmission and/or ER visit)

    30 days post -discharge

Study Arms (2)

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

Other: 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

Other: Usual careOther: Phone Calls

Interventions

Phone CallsUsual Care
Phone Calls

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodProbability Sample
Study Population

Newly diagnosed older colon cancer patients require pre-operative evaluation before undergoing surgery.

You may qualify if:

  • Age 65 or older.
  • Newly diagnosed cancer.
  • Referred to the geriatrics service for pre-operative evaluation before surgical resection of his/her tumor.

You may not qualify if:

  • Inability to comprehend English.
  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Memorial Sloan Kettering Cancer Center

New York, New York, 10065, United States

Location

Related Links

MeSH Terms

Conditions

Colonic Neoplasms

Condition Hierarchy (Ancestors)

Colorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal Diseases

Study Officials

  • Armin Shahrokni, MD, PhD

    Memorial Sloan Kettering Cancer Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 21, 2014

First Posted

November 25, 2014

Study Start

November 1, 2014

Primary Completion

March 16, 2016

Study Completion

March 16, 2016

Last Updated

March 13, 2017

Record last verified: 2017-03

Locations